Table of Contents

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549


FORM 10-Q

(Mark One)

xQUARTERLY REPORT PURSUANT TO SECTION
Quarterly report pursuant to Section 13 ORor 15(d) OF THE SECURITIES EXCHANGE ACT OFof the SecuritiesExchange Act of 1934

For the quarterly period ended June 30, 2020

OR

2023
or
¨TRANSITION REPORT PURSUANT TO SECTION
Transition report pursuant to Section 13 ORor 15(d) OF THE SECURITIES EXCHANGE ACT OFof the SecuritiesExchange Act of 1934

Therapeutics Acquisition Corp.

For the transition period from ______to ______.

Commission file number: 001-39311

POINT BIOPHARMA GLOBAL INC.
(Exact name of registrant as specified in its charter)

Delaware001-3937385-0800493
Delaware85-0800493
(State or other jurisdiction
of incorporation)
(Commission
File Number)
(IRS Employer
Identification No.)
incorporation or organization)
4850 West 78th Street
Indianapolis,IN46268
(Address of principal executive offices)(Zip Code)

200 Berkeley Street

18th Floor

Boston, MA 02116

(Address of principal executive offices, including zip code)


Registrant’s telephone number, including area code: (617) 778.2500

Not Applicable
(Former name or former address, if changed since last report)

(317) 543-9957

Securities registered pursuant to Section 12(b) of the Act:


Title of each classTrading Symbol(s)Trading
Symbol(s)
Name of each exchange on
which
registered
Class A common stock, par value $0.0001 per share  Common StockPNTRACATheNasdaqThe Nasdaq StockCapital Market LLC


Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yesx No ¨

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files).

Yes x No ¨

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

Large accelerated filer¨Accelerated filer¨
Non-accelerated filerxSmaller reporting companyx
Emerging growth companyx

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ¨

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes x No ¨

As

Indicate the number of August 14, 2020, 14,041,000 Class Ashares outstanding of each of the issuer’s classes of common stock, as of the latest practicable date.
Common Stock, par value $0.0001 and 3,392,500 Class B common stock, par value $0.0001, were issued and outstanding.

per share – 105,765,954
shares outstanding as of August 9, 2023.

Therapeutics Acquisition Corp.

d/b/a Research Alliance Corp. I

Quarterly Report on Form 10-Q


Table of Contents

Content
s
INDEX
Page No. 

Unaudited Condensed Financial Statements
2
Unaudited Condensed Statement of Changes in Stockholders’ Equity for the period from April 15, 2020 (inception) through June 30, 20203
Unaudited Condensed StatementConsolidated Statements of Cash Flows for the period from April 15, 2020 (inception) through Six Months ended June 30, 2020 30, 2023 and June 30, 2022
Management’s Management's Discussion and Analysis of Financial Condition and Results of Operations
Quantitative and Qualitative Disclosures Aboutabout Market Risk
Controls and Procedures
22
Item 1A.Risk Factors22
Unregistered Sales of Equity Securities and Use of Proceeds from Registered Securities
Defaults Upon Senior Securities
Mine Safety Disclosures
23
Exhibits23
SIGNATURES



PART I -I. FINANCIAL INFORMATION

Item 1. Unaudited

ITEM 1 – FINANCIAL STATEMENTS
POINT Biopharma Global Inc.
Interim Condensed Financial Statements.

THERAPEUTICS ACQUISITION CORP.

d/b/a RESEARCH ALLIANCE CORP. I

UNAUDITED Condensed BALANCE SHEET

  June 30, 2020 
ASSETS    
Cash $64,690 
Total Current Assets  64,690 
Deferred offering costs  449,452 
Total Assets $514,142 
LIABILITIES AND STOCKHOLDERS’ EQUITY    
Current liabilities:    
Accounts payable $6,108 
Accrued expenses  227,403 
Notes payable – related party  275,000 
Total Current Liabilities  508,511 
Commitments and Contingencies    
Stockholders’ Equity    
Preferred Stock, $0.0001 par value; 1,000,000 shares authorized; none outstanding    - 
Class A common stock, $0.0001 par value; 100,000,000 shares authorized, none outstanding  - 
Class B common stock, $0.0001 par value; 10,000,000 shares authorized; 3,392,500 issued and outstanding(1)  339 
Additional paid-in capital  24,661 
Accumulated deficit  (19,369)
Total Stockholders’ Equity  5,631 
TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY $514,142 

(1) This number includes up to 442,500 shares of Class B common stock held by the Sponsor that were subject to forfeiture if the over-allotment option is not exercised in full or in part by the underwriters. On July 10, 2020, the underwriters exercised the over-allotment option in full; thus, these shares are no longer subject to forfeiture.

TheConsolidated Balance Sheets

(In U.S. dollars)
June 30, 2023
(Unaudited)December 31, 2022
$$
ASSETS  
Current assets  
Cash and cash equivalents57,293,338 286,428,371 
Short-term investments365,932,523 238,783,470 
Prepaid expenses and other current assets5,750,433 5,610,889 
Income taxes receivable3,399,009 — 
Total current assets432,375,303 530,822,730 
Non-current assets
Long-term investments11,570,701 16,119,430 
Note receivable5,028,767 — 
Property, plant and equipment, net48,394,217 31,380,576 
Operating lease right-of-use asset405,784 — 
Total non-current assets65,399,469 47,500,006 
Total assets497,774,772 578,322,736 
LIABILITIES & STOCKHOLDERS' EQUITY
Current liabilities
Accounts payable13,899,941 7,703,150 
Accrued liabilities10,099,052 19,094,454 
Deferred revenue15,899,770 23,242,290 
Income taxes payable— 29,698,546 
Finance lease current liability1,011,217 — 
Operating lease current liability245,814 — 
Total current liabilities41,155,794 79,738,440 
Deferred revenue, net of current portion3,197,547 10,178,147 
Long-term income taxes payable1,452,356 1,452,356 
Finance lease liability, net of current portion4,348,112 — 
Operating lease liability, net of current portion169,045 — 
Total liabilities50,322,854 91,368,943 
Commitments and contingencies (Note 12)
Stockholders’ equity
Common Stock, par value $0.0001 per share, 430,000,000 authorized, 105,765,954 and 105,649,741 issued and outstanding as of June 30, 2023 and December 31, 2022, respectively10,576 10,565 
Additional paid-in capital451,443,330 448,391,574 
Retained earnings(2,933,005)39,008,505 
Accumulated other comprehensive loss(1,068,983)(456,851)
Total stockholders’ equity447,451,918 486,953,793 
Total liabilities and stockholders’ equity497,774,772 578,322,736 
See accompanying notes are an integral partto the unaudited interim condensed consolidated financial statements
1


POINT Biopharma Global Inc.

THERAPEUTICS ACQUISITION CORP.

d/b/a RESEARCH ALLIANCE CORP. I

UNAUDITED

Unaudited Interim Condensed STATEMENT OF OPERATIONS

  For the period from
April 15, 2020
(inception)
through June 30, 2020
 
Formation and operating costs $19,369 
Net loss $(19,369)
Weighted average shares outstanding, basic and diluted(1)  3,392,500 
Basic and diluted net loss per share $(0.01)

(1) This number includes an aggregate Consolidated Statements of up to 442,500 shares of Class B common stock held by the Sponsor subject to forfeiture if the over-allotment option is not exercised in full or in part by the underwriters. On July 10, 2020, the underwriters exercised the over-allotment option in full; thus, these shares are no longer subject to forfeitures.

TheOperations

(In U.S. dollars, except share amounts)
For the three months endedFor the six months ended
June 30,
2023
June 30,
2022
June 30,
2023
June 30,
2022
$ $$$
Revenue
Other revenue4,865,856 — 14,323,120 — 
Total revenue4,865,856  14,323,120  
Operating expenses 
Research and development31,276,573 20,813,882 58,187,045 33,314,730 
General and administrative5,088,403 4,080,401 10,098,532 7,888,343 
Total operating expenses36,364,976 24,894,283 68,285,577 41,203,073 
Loss from operations(31,499,120)(24,894,283)(53,962,457)(41,203,073)
Other income (expenses)
Investment income5,335,753 509,700 11,099,967 557,673 
Foreign currency loss(168,770)(12,259)(238,960)(43,900)
Total other income (expenses)5,166,983 497,441 10,861,007 513,773 
Loss before income taxes(26,332,137)(24,396,842)(43,101,450)(40,689,300)
Income tax benefit (provision)921,298 (183,405)1,159,940 (271,521)
Net loss(25,410,839)(24,580,247)(41,941,510)(40,960,821)
Net loss per basic and diluted common share:
Basic and diluted net loss per common share$(0.24)$(0.27)$(0.40)$(0.45)
Basic and diluted weighted average common shares outstanding105,724,215 90,124,295 105,692,615 90,123,288 
See accompanying notes are an integral partto the unaudited interim condensed consolidated financial statements
2


POINT Biopharma Global Inc.

THERAPEUTICS ACQUISITION CORP.

d/b/a RESEARCH ALLIANCE CORP. I

UNAUDITED

Unaudited Interim Condensed STATEMENT OF CHANGES IN STOCKHOLDERS’ EQUITY

  For the period from April 15, 2020 (inception)
through June 30, 2020
 
  Common Stock  Additional     Total 
  Class A  Class B  Paid-In  Accumulated  Stockholders’ 
  Shares  Amount  Shares  Amount  Capital  Deficit  Equity 
Balance – April 15, 2020 (Inception) -  $-   -  $-  $-  $-  $- 
Issuance of common stock to Sponsor(1)  -   -   3,392,500   339   24,661   -   25,000 
Net loss  -   -   -   -   -   (19,369)  (19,369)
Balance – June 30, 2020  -  $-   3,392,500  $339  $24,661  $(19,369) $5,631 

(1) This number includes up to 442,500 shares Consolidated Statements of Class B common stock held by the Sponsor that were subject to forfeiture if the over-allotment option is not exercised in full or in part by the underwriters. On July 10, 2020, the underwriters exercised the over-allotment option in full; thus, these shares are no longer subject to forfeitures.

TheComprehensive Loss

(In U.S. dollars)
For the three months endedFor the six months ended
June 30,
2023
June 30,
2022
June 30,
2023
June 30,
2022
$ $$$
Net loss(25,410,839)(24,580,247)(41,941,510)(40,960,821)
Other comprehensive income, net of tax
Net unrealized loss on available-for-sale debt securities(813,426)(342,378)(612,132)(342,378)
Total comprehensive loss(26,224,265)(24,922,625)(42,553,642)(41,303,199)

See accompanying notes are an integral partto the unaudited interim condensed consolidated financial statements
3


POINT Biopharma Global Inc.

THERAPEUTICS ACQUISITION CORP.

d/b/a RESEARCH ALLIANCE CORP. I

UNAUDITED

Unaudited Interim Condensed STATEMENT OF CASH FLOWS

  Period From April 15, 2020
(Inception)
to June 30, 2020
 
Cash Flows from Operating Activities    
Net loss $(19,369)
Changes in operating assets and liabilities:    
Accounts payable  1,363 
Net cash used in operating activities  (18,006)
     
Cash Flows from Financing Activities:    
Proceeds from issuance of common stock to Sponsor  25,000 
Deferred offering costs  (217,304)
Proceeds from related party note  275,000 
Net cash provided by financing activities  82,696 
     
Net Change in Cash  64,690 
Cash – beginning of the period  - 
Cash – end of the period $64,690 
     
Non-cash investing and financing activities:    
Deferred offering costs included in accrued offering costs $227,403 
Deferred offering costs included in accounts payable $4,745 

The Consolidated Statements of Stockholders’ Equity

(In U.S. dollars, except share amounts)
Common StockAdditional
Paid-in Capital
Accumulated DeficitAccumulated Other Comprehensive LossTotal Equity
Number Amount   
 # $ $ $$ $
Balance at December 31, 2022105,649,741 10,565 448,391,574 39,008,505 (456,851)486,953,793 
Issuance of shares of Common Stock in connection with stock option exercises32,936 145,861 — — 145,864 
Stock-based compensation— — 1,009,496 — — 1,009,496 
Net loss— — — (16,530,671)— (16,530,671)
Other comprehensive income, net of tax— — — — 201,294 201,294 
Balance at March 31, 2023105,682,677 10,568 449,546,931 22,477,834 (255,557)471,779,776 
Issuance of shares of Common Stock in connection with stock option exercises83,277 186,050 — — 186,058 
Stock-based compensation— — 1,710,349 — — 1,710,349 
Net loss— — — (25,410,839)— (25,410,839)
Other comprehensive loss, net of tax— — — — (813,426)(813,426)
Balance at June 30, 2023105,765,954 10,576 451,443,330 (2,933,005)(1,068,983)447,451,918 
Common StockAdditional
Paid-in
Capital
Accumulated
Deficit
Accumulated Other Comprehensive LossTotal Equity
Number Amount   
 # $ $ $$ $
Balance at December 31, 202190,121,794 9,012 314,488,782 (59,284,708) 255,213,086 
Issuance of shares of Common Stock in connection with stock option exercises678 — 942 — — 942 
Stock-based compensation— — 440,450 — — 440,450 
Net loss— — — (16,380,574)— (16,380,574)
Balance at March 31, 202290,122,472 9,012 314,930,174 (75,665,282) 239,273,904 
Issuance of shares of Common Stock in connection with stock option exercises2,490 — 3,461 — — 3,461 
Stock-based compensation— — 1,027,563 — — 1,027,563 
Net loss— — — (24,580,247)— (24,580,247)
Other comprehensive loss, net of tax— — — — (342,378)(342,378)
Balance at June 30, 202290,124,962 9,012 315,961,198 (100,245,529)(342,378)215,382,303 
See accompanying notes are an integral partto the unaudited interim condensed consolidated financial statements
4

POINT Biopharma Global Inc.
Unaudited Interim Condensed Consolidated Statements of Cash Flows
(In U.S. dollars)
For the six months ended
June 30, 2023June 30, 2022
$$
Cash flows from operating activities  
Net loss:(41,941,510)(40,960,821)
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation on property, plant and equipment1,322,329 584,076 
Stock-based compensation expense2,719,845 1,468,013 
Operating lease expense50,499 — 
Payments on operating lease(49,321)— 
Amortization of premiums (accretion of discounts) on investments, net(7,066,456)(128,150)
Changes in operating assets and liabilities:
Prepaid expenses and other current assets(139,544)(441,829)
Accounts payable4,285,143 4,290,469 
Accrued liabilities(9,178,905)3,734,644 
Deferred revenue(14,323,120)— 
Income taxes receivable and payable(33,097,555)258,425 
Change in accrued interest and dividends within investments691,359 126,192 
Net cash used in operating activities(96,727,236)(31,068,981)
Cash flows from investing activities
Purchase of investments, net of sales and maturities(116,749,966)(126,563,131)
Purchase of property, plant and equipment(10,856,112)(3,080,040)
Purchase of note receivable(5,000,000)— 
Net cash used in investing activities(132,606,078)(129,643,171)
Cash flows from financing activities
Issuance of shares of Common Stock in connection with stock option exercises331,922 4,403 
Payments on finance lease(133,641)— 
Net cash provided by financing activities198,281 4,403 
Net decrease in cash and cash equivalents(229,135,033)(160,707,749)
Cash and cash equivalents, beginning of period286,428,371 238,815,991 
Cash and cash equivalents, end of period57,293,338 78,108,242 
Supplemental disclosure of cash flow information:
Cash paid for income taxes31,913,750 3,022 
Non-cash investment activities:
Purchase of property, plant and equipment recorded in accounts payable and accrued liabilities3,504,652 3,345,729 

See accompanying notes to the unaudited interim condensed consolidated financial statements.

statements

5

THERAPEUTICS ACQUISITION CORP.

d/b/a RESEARCH ALLIANCE CORP. I


Table of ContentNOTES TO UNAUDITED s
Notes to the Unaudited Interim Condensed FINANCIAL STATEMENTS

1.Organization, Business Operations and Basis of Presentation

Therapeutics Acquisition Corp. d/b/a Research Alliance Corp. I (the "Company" Consolidated Financial Statements


1. Nature of business
POINT Biopharma Global Inc., together with its consolidated subsidiaries ("POINT" or the “Company”), is a blank checkglobally focused radiopharmaceutical company incorporated on April 15, 2020 (inception) asbuilding a Delaware corporationplatform for the purposeclinical development and commercialization of effecting a merger, capital stock exchange, asset acquisition, share purchase, reorganization or similar business combination with one or more businesses (the "Business Combination"). While the Company may pursue an acquisition opportunity in any business, industry, sector or geographical location, it intends to focus on industriesradioligands that complement its management team's background, and to capitalize on the ability of its management team to identify and acquire a business, focusing on the healthcare industry. In particular, the Company will target companies in the biotechnology sector where its management has extensive investment experience.fight cancer. The Company is an emerging growth companywas founded on a mission to make radioligand therapy applicable to more cancers and as such,available to more people, thereby improving the Company is subject to alllives of the risks associated with emerging growth companies.

As of June 30, 2020, the Company had not commenced any operations. All activity for the period from April 15, 2020 (inception) through June 30, 2020 relates to the Company's formationcancer patients and the initial public offering (the "Initial Public Offering") described below. The Company will not generate any operating revenues until after the completion of its initial Business Combination, at the earliest. The Company will generate non-operating income in the form of interest income on cash and cash equivalents from the proceeds derived from the Initial Public Offering. their families everywhere.

The Company has selected December 31 as its fiscal year end.

The Company's sponsor is Therapeutics Acquisition Holdingsfour wholly-owned subsidiaries, POINT Biopharma Inc., POINT Biopharma USA Inc. and West 78th Street, LLC, a Delaware limited liability company (the "Sponsor"). The registration statement for the Company’s Initial Public Offering was declared effective on July 7, 2020. On July 10, 2020, the Company consummated the Initial Public Offering, and sold 13,570,000 shares of Class A common stock for $10.00 per share, generating gross proceeds of $135.7 million, and incurring offering costs of approximately $8.1 million, inclusive of approximately $4.8 million in deferred underwriting commissions (Note 5).

Concurrently with the closing of the Initial Public Offering, the Company completed the private sale of 471,400 shares of Class A Common Stock (the "Private Placement Shares") at a purchase price of $10.00 per Private Placement Share, to the Sponsor, generating gross proceeds to the Company of approximately $4.7 million. The Private Placement Shares are identical to the Class A Common Stock soldeach located in the Initial Public Offering, except that, so long as they are held by the SponsorU.S., and their permitted transferees: (i) they may not, subject to certain limited exceptions, be transferred, assigned or sold by the Sponsor until the earlier of (A) one year after the completion of the Company’s initial Business Combination or (B) subsequent to the Company’s initial Business Combination, the date on which the Company completes a liquidation, merger, capital stock exchange, reorganization or other similar transaction that results in all of the Company’s stockholders having the right to exchange their common stock for cash, securities or other property, and (ii) they are entitled to registration rights. Additionally, if the closing price of the Company’s common stock equals or exceeds $12.00 per share (as adjusted for stock splits, stock capitalizations, reorganizations, recapitalizations and the like) for any 20 trading days within any 30-trading day period commencing at least 150 days after the Company’s initial Business Combination, the Private Placement Shares will be released from the lock-up. In addition, the Sponsor has agreed to waive its redemption rights with respect to the Private Placement Shares in connection with (i) the consummation of the Company’s initial Business Combination, including, without limitation, any such rights available in the context of a stockholder vote to approve such Business Combination, or (ii) a stockholder vote to approve an amendment to the Company’s second amended and restated certificate of incorporation to modify the substance or timing of the Company’s obligation to redeem 100% of the shares of Class A common stock sold in the Company’s Initial Public Offering if the Company has not consummated a Business Combination within 24 months of the closing of its Initial Public Offering or with respect to any other material provisions relating to our stockholders’ rights or pre-initial Business Combination activity or in the context of a tender offer made by the Company to purchase Offering Shares (although the Sponsor, shall be entitled to redemption and liquidation rights with respect to any Initial Public Offering shares it holds if the Company fails to consummate a Business Combination within 24 months of the closing of the Initial Public Offering).


The Company's management has broad discretion with respect to the specific application of the net proceeds of the Company’s Initial Public Offering and the sale of the Private Placement shares, although substantially all of the net proceeds are intended to be applied generally toward consummating a Business Combination. There is no assurance that the Company will be able to complete a Business Combination successfully. The Company must complete one or more initial Business Combinations having an aggregate fair market value of at least 80% of the assets held in the Trust Account (as defined below) (excluding the deferred underwriting commissions and taxes payable on income earned on the Trust Account) at the time of the agreement to enter into the initial Business Combination. However, the Company will only complete a Business Combination if the post-transaction company owns or acquires 50% or more of the outstanding voting securities of the target or otherwise acquires a controlling interest in the target sufficient for it not to be required to register as an investment company under the Investment Company Act of 1940, as amended (the "Investment Company Act"). Upon the closing of the Initial Public Offering, $135,700,000 ($10 per share) of the net proceeds of the Initial Public Offering and certain of the proceeds of the Private Placement Shares were placed in a trust account ("Trust Account")POINT Biopharma Corp., located in Canada (collectively the United States at JP Morgan Chase Bank, N.A., maintained by Continental Stock Transfer & Trust Company, acting as trustee, and invested only in U.S. government securities, within the meaning set forth in Section 2(a)(16) of the Investment Company Act, with a maturity of 185 days or less or in any open-ended investment company that holds itself out as a money market fund selected by the Company meeting the conditions of paragraphs (d)(2), (d)(3) and (d)(4) of Rule 2a-7 of the Investment Company Act, as determined by the Company, until the earlier of: (i) the completion of a Business Combination and (ii) the distribution of the assets held in the Trust Account as described below.

The Company will provide the holders of its outstanding shares of Class A common stock, par value $0.0001 (the "Class A common stock""Subsidiaries"), sold in the Initial Public Offering (the "Stockholders") with the opportunity to redeem all or a portion of their Public Shares (as defined in Note 3) upon the completion of a Business Combination either (i) in connection with a stockholder meeting called to approve the Business Combination or (ii) by means of a tender offer. The decision as to whether the Company will seek stockholder approval of a Business Combination or conduct a tender offer will be made by the Company, solely in its discretion. The Stockholders will be entitled to redeem their Public Shares for a pro rata portion of the amount then in the Trust Account (initially anticipated to be $10.00 per Public Share). The per-share amount to be distributed to Stockholders who redeem their Public Shares will not be reduced by the deferred underwriting commissions the Company will pay to the underwriters (as discussed in Note 5). These Public Shares will be recordedCompany’s headquarters is located at a redemption value and classified as temporary equity upon the completion4850 West 78th Street, Indianapolis, Indiana, 46268.

2. Summary of the Initial Public Offeringsignificant accounting policies
Basis of presentation
The accompanying unaudited interim condensed consolidated financial statements have been prepared in accordance with the Financial Accounting Standards Board's ("FASB"Board (“FASB”) Accounting Standards Codification ("ASC"(“ASC”) Topic 480 "Distinguishing Liabilities from Equity." In such case,270, Interim Reporting and include the Company will proceed with a Business Combination if the Company has net tangible assets of at least $5,000,001 upon such consummation of a Business Combination and a majority of the shares voted are voted in favor of the Business Combination. If a stockholder vote is not required by law and the Company does not decide to hold a stockholder vote for business or other legal reasons, the Company will, pursuant to its second amended and restated certificate of incorporation, conduct the redemptions pursuant to the tender offer rules of the U.S. Securities and Exchange Commission ("SEC") and file tender offer documents with the SEC prior to completing a Business Combination. If, however, stockholder approval of the transactions is required by law, or the Company decides to obtain stockholder approval for business or legal reasons, the Company will offer to redeem shares in conjunction with a proxy solicitation pursuant to the proxy rules and not pursuant to the tender offer rules. Additionally, each Stockholder may elect to redeem their Public Shares irrespective of whether they vote for or against the proposed transaction. If the Company seeks stockholder approval in connection with a Business Combination, the Company’s Sponsor, directors and executive officers have agreed to vote their Founder Shares (as defined below in Note 4), Private Placement Shares and any Public Shares purchased during or after the Initial Public Offering in favor of a Business Combination. In addition, the Company’s Sponsor, directors and executive officers have agreed to waive its redemption rights with respect to their Founder Shares, Private Placement Shares and Public Shares owned by it in connection with the completion of a Business Combination.


Notwithstanding the foregoing, the Company's second amended and restated certificate of incorporation provides that a Stockholder, together with any affiliate of such stockholder or any other person with whom such stockholder is acting in concert or as a "group" (as defined under Section 13 of the Securities Exchange Act of 1934, as amended (the "Exchange Act")), will be restricted from redeeming its shares with respect to more than an aggregate of 15% or more of the shares of Class A common stock sold in the Initial Public Offering, without the prior consent of the Company.

The Sponsor, directors and executive officers have agreed not to propose an amendment to the second amended and restated certificate of incorporation to modify the substance or timing of the Company's obligation to redeem 100% of its Public Shares if the Company does not complete a Business Combination or with respect to any other material provisions relating to stockholders' rights or pre-initial Business Combination activity, unless the Company provides the stockholders with the opportunity to redeem their shares of Class A common stock in conjunction with any such amendment.

If the Company is unable to complete a Business Combination within 24 months from the closing of the Initial Public Offering, or July 10, 2022 (the "Combination Period"), the Company will (i) cease all operations except for the purpose of winding up, (ii) as promptly as reasonably possible but not more than ten business days thereafter, redeem the Public Shares, at a per-share price, payable in cash, equal to the aggregate amount then on deposit in the Trust Account including interest earned on the funds held in the Trust Account and not previously released to the Company to pay its income taxes (less up to $100,000 of interest to pay dissolution expenses), divided by the number of then outstanding Public Shares, which redemption will completely extinguish Stockholders' rights as stockholders (including the right to receive further liquidating distributions, if any), subject to applicable law, and (iii) as promptly as reasonably possible following such redemption, subject to the approval of the Company's remaining stockholders and the Company's board of directors, proceed to commence a voluntary liquidation and thereby a formal dissolutionaccounts of the Company subject in each case to the Company's obligations to provide for claims of creditors and the requirements of other applicable law.

The Sponsor, directors and executive officers have agreed to waive their liquidation rights with respect to the Founder Shares and Private Placement shares if the Company fails to complete a Business Combination within the Combination Period. However, if the Sponsor, directors or executive officers acquire Public Shares in or after the Initial Public Offering, they will be entitled to liquidating distributions from the Trust Account with respect to such Public Shares if the Company fails to complete a Business Combination within the Combination Period. The underwriters have agreed to waive their rights to their deferred underwriting commission (see Note 5) held in the Trust Account in the event the Company does not complete a Business Combination within in the Combination Period and, in such event, such amounts will be included with the funds held in the Trust Account that will be available to fund the redemption of the Company's Public Shares. In the event of such distribution, it is possible that the per share value of the residual assets remaining availableSubsidiaries, for distribution (including Trust Account assets) will be only $10.00 per share initially held in the Trust Account (or less than that in certain circumstances). In order to protect the amounts held in the Trust Account, the Sponsor has agreed to be liable to the Company if and to the extent any claims by a vendor for services rendered or products sold to the Company, or a prospective target business with which the Company has discussed entering into a transaction agreement, reduce the amount of funds in the Trust Account. This liability will not apply with respect to any claims by a third party who executed a waiver of any right, title, interest or claim of any kind in or to any monies held in the Trust Account or to any claims under the Company's indemnity of the underwriters of the Initial Public Offering against certain liabilities, including liabilities under the Securities Act of 1933, as amended (the "Securities Act"). Moreover, in the event that an executed waiver is deemed to be unenforceable against a third party, the Sponsor will not be responsible to the extent of any liability for such third party claims. The Company will seek to reduce the possibility that the Sponsor will have to indemnify the Trust Account due to claims of creditors by endeavoring to have all vendors, service providers (except for the Company's independent registered public accounting firm), prospective target businesses or other entities with which the Company does business, execute agreements with the Company waiving any right, title, interest or claim of any kind in or to monies held in the Trust Account.


Note 2 — Summary of Significant Accounting Policies

Basis of Presentation

The accompanying unaudited condensed financial statements are presented in U.S. dollars in conformity with accounting principles generally accepted in the United States of America ("U.S. GAAP") for interim financial information and pursuant to the rules and regulations of the SEC.Securities and Exchange Commission ("SEC"). Accordingly, they do not include all of the information and footnotes required by U.S. GAAP.accounting principles generally accepted in the United States of America (“GAAP”). All intercompany accounts and transactions have been eliminated in consolidation. In the opinion of management, the unaudited interim condensed consolidated financial statements reflect all adjustments, which include only normal recurring adjustments, necessary for the fair statement of the balances and results for the periods presented. Operating resultsExcept as described below, the accounting policies and methods of computation applied in the unaudited interim condensed consolidated financial statements and related notes contained therein are consistent with those applied by the Company in its audited consolidated financial statements as of and for the period from April 15, 2020 (inception) through June 30, 2020 are not necessarily indicative of the results that may be expected throughyear ended December 31, 2020.

The accompanying2022 contained in our Annual Report on Form 10-K for the year ended December 31, 2022, as filed with the SEC on March 27, 2023 (the “2022 Financial Statements”). These unaudited interim condensed consolidated financial statements should be read in conjunction with the audited2022 Financial Statements.

These unaudited interim condensed consolidated financial statements and accompanying notes thereto includedhave been prepared in accordance with the provisions of ASC Topic 205-40, Presentation of Financial Statements—Going Concern on the basis that the Company will continue as a going concern, which contemplates the realization of assets and the settlement of liabilities and commitments in the final prospectus filed bynormal course of business.
Impact of COVID-19 Pandemic, macroeconomics and other geopolitical events
Although the World Health Organization declared in early May of 2023 that COVID-19 no longer constitutes a public health emergency, the Company withcontinues to actively monitor the SECCOVID-19 developments and potential impact on July 9, 2020the Company's employees, business and with the audited balance sheet includedoperations. The impact from global economic conditions and potential and continuing disruptions to and volatility in the Form 8-K filed bycredit and equity markets in the Company with the SEC on July 16, 2020.

Emerging Growth Company

United States and worldwide are highly uncertain and cannot be predicted. The Company is an "emerging growth company,"currently operating in a period of significant economic uncertainty, resulting from, among other things, the impact of the COVID-19 pandemic, geopolitical tensions, such as the ongoing military conflict between Russia and Ukraine and heightened tensions between China and Taiwan, trade uncertainty, including changes in tariffs, sanctions, international treaties, and other trade restrictions, rising inflation and interest rates, and uncertainty and liquidity concerns in the broader financial services industry, including those caused by certain recent banking failures.


The Company is continuing to monitor the development and potential impact of these global economic and geopolitical events on its business and unaudited interim condensed consolidated financial statements. To date, the Company has not experienced any material business disruptions or incurred any impairment losses in the carrying values of its assets as a result of these events and it is not aware of any specific related event or circumstance that would require it to revise its estimates reflected in these unaudited interim condensed consolidated financial statements. However, estimates and assumptions about future events and their effects cannot be determined with certainty and therefore require the exercise of judgment; as a result, the Company’s estimates may change as new events occur and additional information is obtained.
Risks and uncertainties
Except for the upfront payment received pursuant to the Lantheus License Agreements (as defined in Section 2(a)Note 3 below), the Company has incurred significant net losses and has funded operations primarily through equity financings. Operating losses and negative cash flows were incurred in the three and six months ended June 30, 2023 and are expected to continue
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to be incurred in future periods. The Company is subject to risks and uncertainties common to early-stage companies in the Securities Act, as modified by the Jumpstart our Business Startups Act of 2012 (the "JOBS Act"), and it may take advantage of certain exemptions from various reporting requirements that are applicable to other public companies that are not emerging growth companiesbiotechnology industry, including, but not limited to, not being required to comply with the auditor attestation requirementssuccessful discovery and development of Section 404 of the Sarbanes-Oxley Act, reduced disclosure obligations regarding executive compensation in its periodic reports and proxy statements, and exemptions from the requirements of holding a nonbinding advisory vote on executive compensation and stockholderproduct candidates, regulatory approval of any golden parachute payments not previously approved.

Further, section 102(b)(1)its product candidates, development by competitors of new technological innovations, dependence on key personnel, the JOBS Act exempts emerging growth companiesability to attract and retain qualified employees, protection of proprietary technology, compliance with governmental regulations, the impact of macroeconomic disruptions, such as those arising from being requiredpublic health crisis or military conflicts and adverse developments affecting the financial services industry, the ability to comply with new or revised financial accounting standards until private companies (thatsecure additional capital to fund operations and commercial success of its product candidates. Product candidates currently under development will require extensive preclinical and clinical testing and regulatory approval prior to commercialization. These efforts require significant amounts of capital, adequate personnel, and infrastructure and extensive compliance-reporting capabilities. Even if the Company’s drug development efforts are successful, it is those that have not had a Securities Act registration statement declared effective or do not have a class of securities registered under the Exchange Act) are required to comply with the new or revised financial accounting standards. The JOBS Act provides that an emerging growth company can elect to opt out of the extended transition period and comply with the requirements that apply to non-emerging growth companies but any such election to opt out is irrevocable. The Company has elected not to opt out of such extended transition period, which means thatuncertain when, a standard is issued or revised and it has different application dates for public or private companies,if ever, the Company as an emerging growth company, can adopt the new or revised standard at the time private companies adopt the new or revised standard.

This may make comparison of the Company's financial statements with another public company which is neither an emerging growth company nor an emerging growth company which has opted out of using the extended transition period difficult or impossible because of the potential differences in accounting standards used.


Net Loss Per Share of Common Stock

The Company complies with accounting and disclosure requirements of FASB ASC Topic 260, "Earnings Per Share." Net loss per share is computed by dividing net loss by the weighted average number of shares of common stock outstanding during the period. This number includes an aggregate of up to 442,500 shares of Class B common stock held by the Sponsor subject to forfeiture if the over-allotment option is not exercised in full or in part by the underwriters. On July 10, 2020, the underwriters exercised the over-allotment option in full; thus, these shares are no longer subject to forfeiture. At June 30, 2020, the Company did not have any dilutive securities and other contracts that could, potentially, be exercised or converted into common stock and then share in the earnings of the Company. As a result, diluted loss per share is the same as basic loss per share for the period presented.

Concentration of Credit Risk

Financial instruments that potentially subject the Company to concentrations of credit risk consist of cash accounts in a financial institution, which, at times, may exceed the Federal Depository Insurance Coverage of $250,000. As of June 30, 2020, the Company has not experienced losses on these accounts and management believes the Company is not exposed towill realize significant risks on such accounts.

Financial Instruments

The fair value of the Company's assets and liabilities, which qualify as financial instruments under the FASB ASC 820, "Fair Value Measurements and Disclosures," approximates the carrying amounts represented in the unaudited condensed balance sheet.

revenue from product sales.

Use of Estimates

estimates

The preparation of the unaudited interim condensed consolidated financial statements in conformity with U.S. GAAP requires the Company's management to make estimates, judgments and assumptions that affect the reported amounts of assets and liabilities, andrelated disclosure of contingent assets and liabilities at the date of the unaudited interim condensed consolidated financial statements, and the reported amounts of expenses duringfor the reporting period.periods presented. Significant estimates and assumptions reflected in these unaudited interim condensed consolidated financial statements include, but are not limited to, the allocation of consideration and the recognition of revenues in respect of the performance obligations under the Lantheus License Agreements, the accrual of research and development expenses, incremental borrowing rates determined in connection with finance and operating lease obligations and the valuations of stock options. The Company bases its estimates on historical experience, known trends and other market-specific or other relevant factors that it believes to be reasonable under the circumstances. On an ongoing basis, management evaluates its estimates when there are changes in circumstances, facts and experience. Changes in estimates are recorded in the period in which they become known. Actual results couldmay differ from those estimates.

Deferred Offering Costs

Deferred offering costs consist of legal, accounting, and other costs incurred through the balance sheet date that are directly related to the Initial Public Offering. $8.1 million of offering-costs and were charged to stockholders’ equity upon the completion of the Initial Public Offering in July 2020.

Income Taxes

estimates or assumptions.

Leases
The Company followsaccounts for leases in accordance with ASC Topic 842, Leases ("ASC 842"). At the assetinception of an arrangement, the Company determines whether the arrangement is or contains a lease based on the unique facts and liability methodcircumstances present. The Company has elected not to recognize leases with an original term of accountingone year or less in the unaudited interim condensed consolidated balance sheets. The Company has also elected to account for income taxes under FASB ASC 740, "Income Taxes." Deferred taxthe lease and non-lease components as a combined lease component for its current lease portfolio. Right-of-use assets and lease liabilities are recognized at the commencement date based on the present value of lease payments over the lease term. Options to renew or early terminate a lease are included in the initial lease term of a lease when there is reasonable certainty that the option will be applied.

ASC 842 requires a lessee to discount its unpaid lease payments using the interest rate implicit in the lease or, if that rate cannot be readily determined, its incremental borrowing rate. The Company's incremental borrowing rate is determined using a secured borrowing rate for the estimated future tax consequences attributable to differences betweensame currency and term as the financial statements carrying amounts of existing assetsassociated lease in a similar economic environment.

Lease expense for operating leases is recognized on a straight-line basis over the lease term and liabilities and their respective tax bases. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable incomeincluded in operating expenses in the years in which those temporary differences are expected to be recovered or settled. The effect on deferred tax assetsunaudited interim condensed consolidated statements of operations and liabilities of a change in tax rates is recognized in income in the period that included the enactment date. Valuation allowances are established, when necessary, to reduce deferred tax assets to the amount expected to be realized.

FASB ASC 740 prescribes a recognition threshold and a measurement attribute for the financial statement recognition and measurement of tax positions taken or expected to be taken in a tax return. For those benefits to be recognized, a tax position must be more likely than not to be sustained upon examination by taxing authorities. There were no unrecognized tax benefits as of June 30, 2020. comprehensive loss.


Recent accounting pronouncements
The Company recognizes accrued interest and penalties related to unrecognized tax benefits as income tax expense. There were no amounts accrued for interest and penalties as of June 30, 2020. The Company is currently not aware of any issues under review that could result in significant payments, accruals or material deviation from its position.


The Company may be subject to potential examination by U.S. federal, U.S. state or foreign taxing authorities in the area of income taxes. These potential examinations may include questioning the timing and amount of deductions, the nexus of income among various tax jurisdictions and compliance with U.S. federal, U.S. state and foreign tax laws. The Company's management does not expect that the total amount of unrecognized tax benefits will materially change over the next twelve months.

Recent Accounting Pronouncements

The Company's management does not believe that anyhas evaluated accounting pronouncements recently issued but not yet effective,adopted and believes that the current accounting pronouncements if currently adopted, woulddo not apply to the Company’s operations and are not expected to have a material effectimpact on the Company'sCompany’s unaudited interim condensed financial statements.

Note 3 — Initial Public Offering

On July 10, 2020, pursuant to the Initial Public Offering, the Company sold 13,570,000 shares of Class A common stock (the “Public Shares”), including the issuance of 1,770,000 shares as a result of the underwriters’ exercise in full of their over-allotment option. The Class A common stock was sold at a price of $10.00 per share, generating gross proceeds to the Company of $135.7 million.

Note 4 — Related Party Transactions

Founder Shares

On April 30, 2020, the Sponsor paid $25,000 in consideration for 2,875,000 shares (the "Founder Shares") of the Company's common stock, par value $0.0001 per share (the "common stock").

On July 8, 2020 the Company effected a 1:1.18 stock split resulting in the initial stockholders holding 3,392,500 Founder Shares, of which up to an aggregate of 442,500 shares were subject to forfeiture. Unless the context otherwise implies, all share and per-share amounts in theseconsolidated financial statements have been retroactively restated to reflect the stock split.

The Company filed an Amendedor disclosures.

3. Revenue
In November 2022, POINT announced strategic collaboration and Restated Certificate of Incorporation on June 15, 2020, such that the Company is authorized to issue shares of Class B common stock. Pursuant to the amendment, the Founder Shares were converted into shares of Class B common stock.

The Founder Shares will automatically convert into shares of Class A common stock at the time of the Company's initial Business Combinationexclusive license agreements with Lantheus Holdings Inc. ("Lantheus") for exclusive worldwide rights for POINT's programs in prostate cancer (PNT2002) and are subject toneuroendocrine tumors (PNT2003), excluding certain transfer restrictions, as described in Note 6. The Company’s Sponsor had agreed to forfeit up to 442,500 Founder Shares to the extent that the over-allotment option was not exercised in full by the underwriters. On July 10, 2020, the underwriters exercised the over-allotment option in full; thus, these Founder Shares are no longer subject to forfeiture.

The Sponsor, directorsterritories (Japan, South Korea, Singapore, Indonesia, and executive officers have agreed, subject to limited exceptions, not to transfer, assign or sell any of its Founder Shares or Private Placement Shares until the earlier to occur of: (A) one year after the completion of the initial Business Combination or (B) subsequent to the initial Business Combination, (x) if the last sale price of the shares of Class A common stock equals or exceeds $12.00 per share (as adjusted for share splits, share dividends, reorganizations, recapitalizationsChina including Hong Kong, Macau and Taiwan) (the "PNT2002 Agreement" and the like)"PNT2003 Agreement", respectively, and collectively the "Lantheus License Agreements"). The collaboration pairs POINT's expertise in next generation radioligand development and manufacturing with Lantheus’ commercial leadership in Prostate-Specific Membrane Antigen ("PSMA") PET and radiopharmaceuticals.


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In December 2022, closing conditions for any 20 trading days within any 30-trading day period commencing at least 150 days after the initial Business Combination, or (y)transaction, including Hart-Scott-Rodino antitrust clearance, were satisfied. POINT received a $250.0 million upfront payment under the date on which the Company completes a liquidation, merger, capital stock exchange or other similar transaction that results in all of the Company's stockholders having the right to exchange their common stock for cash, securities or other property.


Private Placement Shares

Concurrently with the closing of the Initial Public Offering, the Sponsor purchased 471,400 Private Placement Shares, at a price of $10.00 per share in a private placement forPNT2002 Agreement and will receive an aggregate purchase price of $4.7 million. The Private Placement Shares are identical to the shares of Class A common stock sold in the Initial Public Offering, subject to certain limited exceptions as described in Note 1.

The Sponsor and the Company's officers and directors have agreed, subject to limited exceptions, not to transfer, assign or sell any of their Private Placement Shares until 30 days after the completion of the initial Business Combination.

Related Party Loans

On April 30, 2020, the Sponsor agreed to loan the Company an aggregateadditional payment of up to $300,000$250.0 million upon U.S. regulatory approval. In addition, once certain return on investment financial thresholds have been achieved and other conditions satisfied, POINT will be eligible to cover expenses relatedreceive royalties of 20% on all net sales (prior to which there is a period of sales in which the Initial Public Offering pursuant to a promissory note (the "Note"). In May 2020, the Company borrowed $275,000 under the Note. The loan was non-interest bearing and the borrowings outstanding under the Note of $275,000 were repaid in full in July 2020.

In order to finance transaction costs in connection with a Business Combination, the Sponsor or an affiliate of the Sponsor, or certain of the Company's officers and directors may, but are not obligated to, loan the Company funds asroyalty may be required ("Working Capital Loans"). If the Company completes a Business Combination, the Company would repay the Working Capital Loans out of the proceeds of the Trust Account released to the Company. Otherwise, the Working Capital Loans would be repaidbased on only out of funds held outside the Trust Account. In the event that a Business Combination is not completed, the Company may use a portion of the proceeds held outsidegross profit), and contingent upon the Trust Account to repay the Working Capital Loans but no proceeds held in the Trust Account would be used to repay the Working Capital Loans. Except for the foregoing, the termssatisfaction of such Working Capital Loans, if any, have not been determined and no written agreements exist with respect to such loans. The Working Capital Loans would either be repaid upon consummationcertain net sales milestones, additional payments of a Business Combination, without interest, or, at the lender's discretion, up to $1.5$1.3 billion. POINT received a $10.0 million upfront payment under the PNT2003 Agreement, and will receive up to an additional $30.0 million upon U.S. regulatory approval. The PNT2003 Agreement also provides that POINT will receive royalties of such Working Capital Loans may be convertible into Private Placement Shares at a price15% on net sales and, contingent upon the satisfaction of $10.00 per share. Ascertain net sales milestones, an additional payment of June 30, 2020, the Company had no outstanding Working Capital Loans.

Private Placement of Common Stock

The Sponsor has indicated an interestup to purchase $25 million of the Company's common stock in a private placement that would occur concurrently$275.0 million.


In connection with the consummation of the initial Business Combination. The funds from such private placement would be used as part of the consideration to the sellers in the initial Business Combination, and any excess funds from such private placement would be used for working capital in the post-transaction company. However, because indications of interest are not binding agreements or commitments to purchase, the Sponsor may determine not to purchase any such shares, or to purchase fewer shares than it indicated an interest in purchasing. Furthermore,PNT2002 Agreement, the Company is not under any obligationresponsible for completing the Company's multi-center, randomized, open label phase 3 Study evaluating metastatic castration-resistant Prostate cancer using 177Lu-PNT2002 PSMA therapy After Second-line Hormonal treatment (“SPLASH") trial and the parties will work together to sell any such shares.

Note 5 — Commitments and Contingencies

Registration Rights

Holders offile the Founder Shares will be entitled to registration rights with respect to the Founder Shares and Private Placement Shares (in the case of the Founder Shares, only after conversion of such shares into shares of Class A common stock) pursuant to a registration and stockholder rights agreement entered into in connectionNew Drug Application (“NDA”), with the consummation of the Initial Public Offering. Holders of the Founder Shares and Private Placement Shares are entitled to certain demand and "piggyback" registration and stockholder rights. However, the registration and stockholder rights agreement provides that the Company will not permit any registration statement filed under the Securities Act to become effective until the termination of the applicable lock-up period for the securities to be registered. The Company will bear the expensescosts incurred in connection with the filingU.S. Food and Drug Administration ("FDA") submission being borne by Lantheus. Thereafter, Lantheus will be responsible for all additional clinical and regulatory costs in the U.S., as well as all costs for development, clinical trials and regulatory approval in the rest of any such registration statements.

its territories outside the U.S., except Asia.

To determine the appropriate amount of revenue to be recognized under ASC Topic 606, Revenue from Contracts with Customers, the Company performs the following steps: (i) identify the promised goods or services in the contract, (ii) determine whether the promised goods or services are performance obligations, including whether they are distinct in the context of the contract, (iii) measure the transaction price, including the constraint on variable consideration, (iv) allocate the transaction price to the performance obligations and (v) recognize revenue when (or as) the Company satisfies each performance obligation.

Underwriting

In connection with the PNT2002 Agreement,

the Company identified the following performance conditions: (i) the license it conveyed to Lantheus with respect to certain intellectual property, (ii) service provided to complete the SPLASH trial, support the NDA submission and participate in joint steering activities and (iii) manufacturing activities. The Company granteddetermined the underwriterstransaction price under ASC Topic 606 at the inception of the PNT2002 Agreement to be the $250.0 million upfront payment and has allocated this to the first two performance obligations based on a 45-dayrelative standalone selling price basis. The standalone selling prices for the first two performance obligations were determined using the adjusted market assessment approach and the expected cost plus a margin assessment approach, respectively. The Company concluded that variable consideration associated with the product manufacturing relates solely to the manufacturing activities performance obligation on the basis that it believes that the expected margin associated with this consideration is in line with market standards and specifically relates to the Company's efforts to satisfy its manufacturing obligations.

In connection with the PNT2003 Agreement, the Company identified the following performance conditions: (i) the license it conveyed to Lantheus with respect to certain intellectual property, (ii) service provided to complete the necessary submissions for regulatory approval and participate in joint steering activities and (iii) manufacturing activities. The Company determined the transaction price under ASC Topic 606 at the inception of the PNT2003 Agreement to be the $10.0 million upfront payment and has allocated this to the first two performance obligations based on a relative standalone selling price basis. The standalone selling prices for the first two performance obligations were determined using the adjusted market assessment approach and the expected cost plus a margin assessment approach, respectively. The Company concluded that variable consideration associated with the product manufacturing relates solely to the manufacturing activities performance obligation on the basis that it believes that the expected margin associated with this consideration is in line with market standards and specifically relates to the Company's efforts to satisfy its manufacturing obligations.
The Company does not include variable consideration to the extent that it is probable that a significant reversal in the amount of cumulative revenue recognized will occur. Variable consideration in the PNT2002 Agreement and PNT2003 Agreement consists of:
Potential future regulatory milestone payments. The Company concluded that this variable consideration is constrained considering that achievement of the milestones is outside its control and contingent upon the future success of clinical trials and regulatory approval by the FDA and in respect of other territories outside the U.S.
Potential future milestone payments in connection with certain sales targets as well as any future royalties. The Company concluded that these payments qualify for the royalty exception. Under the royalty exception, sales-based royalties are recognized at the later of when (1) the subsequent sale or usage occurs or (2) the performance obligation to which some or all of the sales- or usage-based royalty has been allocated is satisfied (in whole or in part). That is, an entity does not estimate the amount of a sales-based royalty at contract inception; rather, revenue would be recognized when the subsequent sales occur (under the assumption that the associated performance obligation has been satisfied or partially satisfied).
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Potential payments for the manufacturing and supply of commercial product. The Company concluded that this variable consideration is constrained as it is contingent upon future regulatory approvals and the execution of a manufacturing and supply agreement.
The estimate of the Company’s variable consideration to be included in the transaction price is updated at each reporting date as a change in estimate. For the potential future regulatory milestone payments, the Company utilizes the most likely amount approach to determine the amounts recognized and timing of recognition. For the potential payments for manufacturing and supply of commercial product, the Company utilizes the expected value approach to determine the amounts recognized and timing of recognition. Once the constraint is removed, the milestone payments will be accounted for and allocated to the performance obligations.
For the licenses conveyed to Lantheus, the Company recognized revenue upon execution and regulatory approval of the Lantheus License Agreements. The Company concluded that the licenses represent that of functional intellectual property as each has significant standalone functionality and derives a substantial portion of their utility from that standalone functionality.
For the obligations to complete the SPLASH trial, support the NDA submission and participate in joint steering activities in connection with the PNT2002 Agreement as well as the obligations to complete the necessary submissions for regulatory approval and participate in joint steering activities for the PNT2003 Agreement, the Company recognizes revenue using the cost-to-cost method, which it concluded best depicts the transfer of control to the customer. Under the cost-to-cost method, the extent of progress towards completion is measured based on the ratio of actual costs incurred to the total estimated costs expected upon satisfying the identified performance obligation. Under this method, revenue is recorded as a percentage of the estimated transaction price based on the extent of progress towards completion.
The following table presents the Company’s contract liabilities as of June 30, 2023 and December 31, 2022:
June 30, 2023December 31, 2022
Deferred revenue
Deferred revenue, current$15,899,770 $23,242,290 
Deferred revenue, net of current portion3,197,547 10,178,147 
Total$19,097,317 $33,420,437 
At inception of the Lantheus License Agreements, deferred revenue of $34.8 million was recognized in connection with future performance. During the three and six months ended June 30, 2023, the Company recognized $4.9 million and $14.3 million in revenue for services performed (three and six months ended June 30, 2022 — $nil and $nil, respectively). The current portion of deferred revenue reflects the Company’s estimate of the revenue it expects to recognize within the next 12 months. The Company expects to recognize the remainder of the deferred revenue in subsequent periods through the year ending December 31, 2028. No contract assets were recognized in connection with the Lantheus License Agreements, including costs incurred in obtaining the agreements.
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4. Cash, cash equivalents and investments
Cash, cash equivalents and investments consisted of the following:
As of June 30, 2023As of December 31, 2022
Cash$5,540,926 $12,429,627 
Cash equivalents:
Money market funds47,656,269 273,998,744 
Commercial paper4,096,143 — 
Total cash and cash equivalents57,293,338 286,428,371 
Short-term investments
Commercial paper131,797,284 115,156,455 
Corporate bonds102,294,737 45,219,042 
U.S. Government agency debt securities56,130,624 42,577,762 
Asset backed securities75,709,878 35,830,211 
Total short-term investments365,932,523 238,783,470 
Long-term investments
Asset backed securities750,129 16,119,430 
Corporate bonds10,820,572 — 
Total long-term investments11,570,701 16,119,430 
Total cash, cash equivalents and investments$434,796,562 $541,331,271 
Available-for-sale investments
The amortized cost, gross unrealized gains, gross unrealized losses and fair value of available-for-sale investments by type of security as of June 30, 2023 were as follows:

Amortized CostUnrealized GainsUnrealized LossesFair ValueCurrentNon-current
Commercial paper$131,908,748 $15 $(111,479)$131,797,284 $131,797,284 $— 
Corporate bonds113,657,153705$(542,549)113,115,309102,294,73710,820,572 
Asset backed securities76,699,026— (239,019)76,460,00775,709,878750,129 
U.S. Government agency debt securities56,306,438— (175,814)56,130,62456,130,624— 
Total available-for-sale securities$378,571,365 $720 $(1,068,861)$377,503,224 $365,932,523 $11,570,701 

The following table summarizes the fair value of available-for-sale investments based on stated contractual maturities as of June 30, 2023:
Amortized CostFair Value
Due within one year$366,912,175 $365,932,523 
Due between one and five years11,659,190 11,570,701 
Total$378,571,365 $377,503,224 

The primary objective of our investment portfolio is to maintain safety of principal balances, provide sufficient levels of liquidity and enhance overall returns in an efficient manner with acceptable levels of risk. Our investment policy limits interest-bearing security investments to certain types of debt and money market instruments issued by institutions with primarily investment-grade credit ratings, and it places restrictions on maturities and concentration by asset class and issuer.

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During the three and six months ended June 30, 2023, we had no realized gains or losses on available-for-sale investments.
5. Fair value measurements
We measure fair value based on the prices that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants at the measurement date. Fair value measurements are based on a three-tier hierarchy that prioritizes the inputs used to measure fair value. These tiers include the following:
Level 1: Quoted prices (unadjusted) in active markets for identical assets or liabilities that are accessible at the measurement date. The fair value hierarchy gives the highest priority to Level 1 inputs.

Level 2: Observable prices that are based on inputs not quoted on active markets, but corroborated by market data. These inputs include quoted prices for similar assets or liabilities; quoted market prices in markets that are not active; or other inputs that are observable or can be corroborated by observable market data for substantially the full term of the assets or liabilities.

Level 3: Unobservable inputs are used when little or no market data is available. The fair value hierarchy gives the lowest priority to Level 3 inputs.

The following table presents information about the Company’s financial assets and liabilities as of June 30, 2023 that are measured at fair value on a recurring basis and indicates the level of the fair value hierarchy used to determine such fair values:
Level 1Level 2Level 3Total
June 30, 2023
Cash equivalents:
Money market mutual fund$47,656,269 $— $— $47,656,269 
Commercial paper— 4,096,143 — 4,096,143 
Available-for-sale debt securities:
Commercial paper— 131,797,284 — 131,797,284 
Corporate bonds— 113,115,309 — 113,115,309 
Asset backed securities— 76,460,007 — 76,460,007 
U.S. Government agency debt securities56,130,624 — — 56,130,624 
Total$103,786,893 $325,468,743 $ $429,255,636 

Certain of our available-for-sale debt securities, including U.S. Government agency debt securities, are valued using inputs observable in active markets for identical securities and are therefore classified as Level 1 within the fair value hierarchy.

On May 7, 2023, POINT Biopharma Inc. entered into a Convertible Note Purchase Agreement (the "Convertible Note Agreement") with Ionetix Alpha Corporation ("Ionetix-α"), a subsidiary of IONETIX Corporation. On June 1, 2023, the Company purchased $5.0 million in unsecured promissory notes (the "Note Receivable") convertible into common stock of Ionetix-α at a conversion price that is subject to certain conditions as defined in the Convertible Note Agreement. Pursuant to the Convertible Note Agreement, the Company will purchase an additional $5.0 million of the Note Receivable six months following the initial purchase. Management assessed all features in the Convertible Note Agreement to determine embedded derivatives requiring bifurcation. In accordance with the Convertible Note Agreement, Ionetix-α has a voluntary redemption option, subject to certain terms and conditions, and may provide notice to the Company upon which the Company can elect to either redeem the Note Receivable at 150% of principal and interest outstanding or convert it into common stock of Ionetix-α. Management concluded that this put option meets the definition of a derivative and it is not clearly and closely related to the Note Receivable, thus requiring bifurcation from the datehost instrument and recognition at fair value. Further, management concluded the Note Receivable host instrument is to be classified as a loan receivable and therefore is measured at amortized cost but disclosure of fair value is required. Management determined the fair values of both the Note Receivable and embedded derivative under Level 3 in the fair value hierarchy. Management concluded that the fair value of the final prospectus relatingNote Receivable as at June 30, 2023 was equal to its amortized cost and that the fair value of the embedded derivative was nil both at inception of the arrangement and at June 30, 2023.

We did not have any financial liabilities measured at fair value on a recurring basis as of June 30, 2023.

There have been no transfers of assets or liabilities between the fair value measurement levels as of June 30, 2023.
11

6. Prepaid expenses and other current assets
Prepaid expenses and other current assets consisted of the following:
As of June 30, 2023 As of December 31, 2022
$ $
Prepaid clinical trial expenses3,418,491 4,011,419 
Prepaid insurance1,781,969 1,310,314 
Canadian harmonized sales tax receivable332,654 60,222 
Other217,319 228,934 
Total5,750,433 5,610,889 
7. Property, plant and equipment, net
Property, plant and equipment, net consisted of the following:
As of June 30, 2023 As of December 31, 2022
$ $
Land and building18,976,410 18,163,962 
Machinery and equipment10,415,742 5,328,639 
Property, plant and equipment, in development15,459,230 8,434,384 
Facility lease5,384,707 — 
Furniture and fixtures721,595 698,728 
Computer equipment153,891 149,892 
51,111,575 32,775,605 
Less: Accumulated depreciation(2,717,358)(1,395,029)
Total48,394,217 31,380,576 

In July 2020, the Company purchased land and a building in Indianapolis, Indiana (which has been expanded to approximately 81,000 square feet) for the purpose of retrofitting the existing building into a state-of-the-art, Good Manufacturing Practices ("GMP") compliant facility that will support the Company’s drug manufacturing operations. The Company commenced the manufacture of clinical supply in the Indianapolis manufacturing facility in January 2022. Construction continues on the facility to expand capacity.

On February 2, 2023, POINT Biopharma Corp., entered into a Facility Agreement (the "UHN Agreement") with University Health Network (“UHN”), a not-for-profit corporation incorporated under the laws of Canada. Pursuant to the Initial Public OfferingUHN Agreement, the Company was provided access to purchase uputilize a 7,700 square foot, licensed research and development space with cGMP manufacturing suites (the “Facility”) under a lease effective April 1, 2023, which the Company will use to 1,770,000develop and expand its pipeline of next-generation radioligands. The lease is accounted for as a finance lease in accordance with ASC 842 and the right-of-use asset has been included within property, plant and equipment. See Note 9 for additional sharesdetails.

Property, plant and equipment that have finite lives are recorded at cost less accumulated depreciation and impairment losses. Depreciation is expensed from the month the particular asset is available for its intended use, using the straight-line method over the estimated useful life of Class A common stocksuch asset at the following rates, which in each case are intended to cover over-allotments, if any,reduce the carrying value of the asset to the estimated residual value:
Asset CategoryEstimated Useful Life
Computer equipment5 years
Machinery and equipment7 years
Furniture and fixtures7 years
Facility lease7 years
Building20 years
8. Accrued liabilities
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Accrued liabilities consisted of the following:
As of June 30, 2023As of December 31, 2022
$$
Accrued personnel costs3,772,849 7,116,382 
Accrued research and development costs5,233,075 9,645,594 
Accrued corporate legal fees and other professional services666,995 2,068,793 
Accrued costs for purchases of property, plant and equipment289,244 105,741 
Other accrued costs136,889 157,944 
Total10,099,052 19,094,454 
9. Leases
Right-of-use assets and lease liabilities are recognized at $10.00 per share, less underwriting discounts and commissions. The underwriters exercised this option in fullthe commencement date based on July 10, 2020.

The underwriters were entitledthe present value of lease payments over the lease term. ASC 842 requires a lessee to an underwriting discount of $0.20 per share, or approximately $2.7 millionits unpaid lease payments using the interest rate implicit in the aggregate, paid upon the closing of the Initial Public Offering. An additional fee of $0.35 per share,lease or, approximately $4.8 million in the aggregate, willif that rate cannot be payable to the underwriters for deferred underwriting commissions. The deferred underwriting commissions will become payable to the underwriters from the amounts held in the Trust Account solely in the event that the Company completes a Business Combination, subject to the terms of the underwriting agreement.

Risks and Uncertainties

Management continues to evaluate the impact of the COVID-19 pandemic on the industry and has concluded that while it is reasonably possible that the virus could have a negative effect on the Company's financial position, results ofreadily determined, its operations and/or search for a target company, the specific impact isincremental borrowing rate. As an implicit interest rate was not readily determinable in the Company’s current portfolio of leases, the incremental borrowing rate was used based on the information available at the commencement date in determining the present value of lease payments.

On February 2, 2023, POINT Biopharma Corp. entered into the UHN Agreement. The lease commencement date was determined to be April 1, 2023, the date upon which the Company was provided access to the Facility. The lease is accounted for as a finance lease in accordance with ASC 842 and the right-of-use asset has been included within property, plant and equipment. Management concluded that the lease represents a finance lease on the basis that management believes that the lease term covers a substantial portion of the economic life of the primary lease component. See Note 7 for additional details. The initial term of the UHN Agreement will run for five years from the lease commencement date, with an option to renew for additional two-year terms thereafter, subject to certain conditions described in the UHN Agreement. Management included the first option to renew for two years as part of the lease term in determining the right-of-use asset and lease liability. The agreement does not transfer any title in the Facility to the Company. During the term, the Company shall be responsible for day-to-day management, activities and decision-making regarding the Facility. General governance of the Facility will be exercised by the Company and UHN through a joint committee. The joint committee, which will meet quarterly, will have a minimum of six people and will be comprised of an equal number of members from each of the Company and UHN.
On April 12, 2023, the Company entered into an operating lease for laboratory space with a lease term of two years. The lease is recorded separately on the interim condensed consolidated balance sheet as an operating lease right-of-use asset with a related operating lease liability as of June 30, 2023. The agreement does not transfer any title in the datelaboratory space to the Company.

The components of these financial statements. lease expense are as follows:

For the six months ended June 30, 2023For the six months ended June 30, 2022
Operating lease expense$50,499$
Finance lease cost
Amortization of right-of-use asset192,311 — 
Interest on lease liability99,199 — 
Total finance lease cost$291,510$

Supplemental cash flow information related to leases are as follows:

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For the six months ended June 30, 2023For the six months ended June 30, 2022
Cash flow information:
Cash paid for amounts included in the measurement of lease liabilities:
Operating cash flow use from operating leases$49,321 $— 
Operating cash flow use from finance leases$99,199 $— 
Financing cash flow use from finance leases$133,641 $— 
Non-cash activity:
Right-of-use assets obtained in exchange for lease obligations:
Operating lease$453,490 $— 
Finance lease$5,384,707 $— 

The financial statements dofollowing table summarizes the weighted average remaining lease terms for the Company’s leases:

As of June 30, 2023
Weighted-average remaining lease term (in years):
Operating lease1.8
Finance lease6.8

As the interest rate implicit in the leases was not include any adjustmentsreadily determinable at the time that might result from the outcomeleases were evaluated, the Company used its incremental borrowing rate based on the information available in determining the present value of this uncertainty.

Note 6 — Stockholder's Equity

Class A common stocklease payments. The Company’s incremental borrowing rate was based on the term of the lease, the economic environment of the lease and reflect the rate the Company would have had to pay to borrow on a secured basis. Below is information on the weighted average discount rates used at the time that the leases were evaluated:


As of June 30, 2023
Weighted-average discount rates:
Operating lease7.6 %
Finance lease7.7 %

The following table summarizes the future maturities of the Company's lease liabilities as of June 30, 2023:

Operating LeaseFinance Lease
2023$121,091 $505,608 
2024249,446 1,011,217 
202574,938 1,011,217 
2026— 1,011,217 
2027— 1,011,217 
Thereafter— 2,275,237 
Total lease payments$445,475 $6,825,713 
Less: imputed interest(30,616)(1,466,384)
Present value of lease liabilities$414,859 $5,359,329 
10. Stockholders’ equity
The Company is authorized to issue 100,000,000430,000,000 shares of Class A common stock, with a par value of $0.0001 per share. As of June 30, 2020 there were no Class A shares issued or outstanding. Subsequent to the completion of the IPO on July 10, 2020, there was 14,041,000 Class A shares issued and outstanding.

Class B common stock – The Company is authorized to issue 10,000,000 shares of Class B common stock, par value $0.0001 per share. In connection with the filing of the Amended and Restated Certificate of Incorporation, the 3,392,500 shares of common stock that were outstanding became shares of Class B common stock, of which 442,500 share were subject to forfeiture to the extent that the underwriters' over-allotment option was not exercised in full or in part, so that the Company’s Sponsor would collectively own 20.0% of the Company's issued and outstanding shares of common stock after the Public Offering. The underwriters exercised this option in full on July 10, 2020; thus these Founder Shares are no longer subject to forfeiture.

The shares of Class B common stock will automatically convert into shares of Class A common stock at the time of the Company’s initial Business Combination on a one-for-one basis (subject to adjustment for stock splits, stock dividends, reorganizations, recapitalizations and the like)("Common Stock"), and subject to further adjustment as provided herein. In the case that additional shares of Class A common stock, or equity-linked securities, are issued or deemed issued in excess of the amounts offered in this prospectus and related to the closing of the Business Combination, including pursuant to a specified future issuance, the ratio at which shares of Class B common stock shall convert into shares of Class A common stock will be adjusted (unless the Sponsor agrees to waive such adjustment with respect to any such issuance or deemed issuance, including a specified future issuance) so that the numberwell as 20,000,000 of shares of Class A commonpreferred stock, issuable upon conversion of all shares of Class B common stock will equal, in the aggregate, on an as-converted basis, 20% of the sum of the total number of all shares of common stock outstanding upon completion of this offering plus all shares of Class A common stock and equity-linked securities issued or deemed issued in connection with the Business Combination (after giving effect to any redemptions of shares of Class A common stock by public stockholders) (excluding any shares or equity-linked securities issued, or to be issued, to any seller in the Business Combination and any private placement shares). The Company’s Sponsor may also elect to convert their shares of Class B common stock into an equal number of shares of Class A common stock, subject to adjustment as provided above, at any time.


Preferred stock – The Company is authorized to issue 1,000,000 shares of preferred stock,a par value of $0.0001 per share (“Preferred Stock”).

During the three months ended June 30, 2023, the Company issued (a) 71,585 shares of Common Stock in connection with such designations, votingthe exercise of stock options granted to non-employee consultants, resulting in total cash proceeds of $99,503 and other rights(b)
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11,692 shares of Common Stock in connection with the exercise of stock options granted to employees, resulting in total cash proceeds of $86,555. During the six months ended June 30, 2023, the Company issued (i) 86,585 shares of Common Stock in connection with the exercise of stock options granted to non-employee consultants, resulting in total cash proceeds of $120,353 and preferences(ii) 29,628 shares of Common Stock in connection with the exercise of stock options granted to employees and directors, resulting in total cash proceeds of $211,569.

During the three months ended June 30, 2022, the Company issued 2,490 shares of Common Stock in connection with the exercise of stock options issued to non-employee consultants, resulting in total cash proceeds of $3,461. During the six months ended June 30, 2022, the Company issued 3,168 shares of Common Stock in connection with the exercise of stock options issued to non-employee consultants, resulting in total cash proceeds of $4,403.
As of June 30, 2023, the total number of issued and outstanding shares of Common Stock was 105,765,954 (December 31, 2022 — 105,649,741). As of June 30, 2023, there were no issued and outstanding shares of Preferred Stock (December 31, 2022 — nil).
Each share of Common Stock entitles the holder to one vote on all matters submitted to a vote of the Company’s stockholders. Holders of Common Stock are entitled to receive dividends, if any, as may be determineddeclared by the Company’s board of directors (the “Board”). During the three and six months ended June 30, 2023, no cash dividends were declared or paid by the Company (June 30, 2022 — $nil).
The Board has the authority to issue shares of Preferred Stock from time to time on terms it may determine, to divide shares of Preferred Stock into one or more series and to fix the designations, preferences, privileges, and restrictions of Preferred Stock, including dividend rights, conversion rights, voting rights, terms of redemption, liquidation preference, sinking fund terms, and the number of shares constituting any series or the designation of any series to the fullest extent permitted by the Company'sDelaware General Corporation Law ("DGCL"). During the six months ended June 30, 2023, no shares of Preferred Stock were issued by the Company.
11. Stock-based compensation
In March 2020, the board of directors. directors of POINT Biopharma Inc. approved the 2020 Equity Incentive Plan (the “2020 EIP”). The 2020 EIP provided for the granting of incentive and non-qualified stock options, stock appreciation rights, restricted stock units, performance awards and other stock-based awards to employees, directors, and consultants of POINT Biopharma Inc. Effective as of June 30, 2021, the Board adopted the POINT Biopharma Global Inc. 2021 Equity Incentive Plan (the “2021 EIP”) to replace the 2020 EIP and allow the Company to grant equity and equity-based incentive awards to officers, employees, non-employee directors and consultants of the Company. The Company assumed the outstanding equity awards under the 2020 EIP, but no further grants may be made under the 2020 EIP. The 2021 EIP provides that the number of shares reserved and available for issuance under the 2021 EIP will automatically increase each January 1, beginning on January 1, 2022, by 4% of the number of outstanding shares of Common Stock on the immediately preceding December 31, or such lesser amount as determined by the Board. As of January 1, 2023, the number of shares of Common Stock available under the 2021 EIP increased by 4,225,990 for a total of 9,129,858 shares of Common Stock authorized for issuance under the 2021 EIP as of June 30, 2023.
Stock options
The Company recorded $685,263 and $1,131,391 to research and development expenses and $1,025,086 and $1,588,454 to general and administrative expenses for stock-based compensation for the three and six months ended June 30, 2023, respectively (June 30, 2022 — $458,634 and $743,945 to research and development expenses and $568,929 and $724,068 to general and administrative expenses for the three and six months ended, respectively). The Company did not recognize a tax benefit related to stock-based compensation expense during the three and six months ended June 30, 2023 as well as during the three and six months ended June 30, 2022, as the Company had net operating loss carryforwards and recorded a valuation allowance against the deferred tax asset.
The following table summarizes the activity relating to the Company’s stock options.
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Number of
Shares
Weighted
Average Exercise
Price Per Share
($)
Weighted-
Average
Remaining
Contractual
Term (in years)
Outstanding as of December 31, 20225,592,1735.85
Granted3,144,0717.03
Exercised(116,213)2.86
Forfeited(122,887)7.37
Expired(13,551)8.47
Outstanding as of June 30, 20238,483,5936.304.7
Vested and expected to vest as of June 30, 20238,483,5936.304.7
Options exercisable as of June 30, 20232,705,4294.894.0
During the three months ended June 30, 2023, 304,248 stock options were granted to directors of the Company, with a weighted average grant date fair value of $4.75 per share. The vesting terms of these options are such that they vest on the one-year anniversary of the date of grant. During the six months ended June 30, 2023, 3,144,071 stock options were granted, including the 304,248 stock options discussed above as well as 2,839,823 stock options granted to employees of the Company, with a weighted average grant date fair value of $3.76 per share. The vesting terms of the options granted to employees of the Company are such that 25% of the options vest on the one-year anniversary of the date of grant and the remaining 75% of such stock options vest in three equal annual installments thereafter.

During the three months ended June 30, 2022, 243,417 stock options were granted to employees and directors of the Company, with a weighted average grant date fair value of $4.66 per share. During the six months ended June 30, 2022, 1,948,614 stock options were granted to employees and directors of the Company, with a weighted average grant date fair value of $4.59 per share. Except as provided below with respect to options granted to directors, the vesting terms of these options are such that 25% of the options vest on the one-year anniversary of the date of grant and the remaining 75% of such stock options vest in three equal annual installments thereafter. On June 6, 2022, the terms of 128,070 stock options granted to directors of the Company during the quarter were amended to reduce the vesting period to one year. This amendment was accounted for as a modification and there was no material impact to stock-based compensation recorded.

The following table presents the assumptions used in the Black-Scholes-Merton option-pricing model to determine the grant date fair value of stock options granted:
Three months ended June 30, 2023Three months ended June 30, 2022Six months ended June 30, 2023Six months ended June 30, 2022
Risk-free interest rate3.91% - 4.23%2.57% - 3.13%3.71% - 4.23%1.24% - 3.13%
Expected term (in years)3.504.253.50 - 4.254.25 - 5.38
Expected volatility67%74% - 75%67% - 68%72% - 75%
Expected dividend yield—%—%—%—%
During the three months ended June 30, 2023, non-employee consultants of the Company exercised 71,585 stock options with an intrinsic value of $604,767 and employees of the Company exercised 11,692 stock options with an intrinsic value of $32,740, for total cash proceeds to the Company of $186,058.
During the six months ended June 30, 2023, non-employee consultants of the Company exercised 86,585 stock options with an intrinsic value of $700,217, and employees and directors of the Company exercised 29,628 stock options with an intrinsic value of $38,300, for total cash proceeds to the Company of $331,922.
During the three and six months ended June 30, 2022, non-employee consultants of the Company exercised 2,490 and 3,168 stock options with intrinsic values of $16,060 and $19,301, respectively. The exercises resulted in cash proceeds to the Company of $3,461 and $4,403, respectively.
As of June 30, 2020, there2023, the unrecognized stock-based compensation expense related to unvested stock options was no preferred stock outstanding.

Note 7 — Subsequent Events

The$19,343,654 and the estimated weighted average remaining vesting period was 2.3 years.

Performance Share Units
During the year ended December 31, 2022, 146,044 performance share units ("PSUs") were granted to employees of the Company, evaluated subsequent events and transactions that occurred afterwith a grant date fair value of $6.61 per unit based on the balance sheet date throughclosing share price of the Company's Common Stock
16

on the date of grant. The vesting terms of these PSUs are such that 100% vest upon the financial statements were issued. Other than as described in these unaudited condensed financial statements in relation toregulatory approval of PNT2002 by the Company's stock split (Note 4), repayment ofFDA. During the Note (Note 4)three and Initial Public Offering (Note 3) and related transactions,six months ended June 30, 2023, the Company did not identifyrecord any stock-based compensation expense related to these PSUs on the basis that they cannot be considered probable to vest as the regulatory approval requirement is outside the control of the Company and other subsequent eventsthe clinical trial remains ongoing.
12. Commitments and contingencies
Indianapolis facility commitments
The Company is party to certain agreements for the continuing expansion of the manufacturing capabilities of the Indianapolis facility. Effective in the second quarter of 2022, the Company entered into an agreement for the design and build of a commercial manufacturing line. As of June 30, 2023, the Company is committed to aggregate future payments of approximately $20.0 million in connection with these agreements. During the three and six months ended June 30, 2023, approximately $7.4 million and $10.3 million, respectively, has been recorded within property, plant and equipment in connection with these agreements (three and six months ended June 30, 2022 — approximately $3.4 million and $4.0 million, respectively).
Clinical trial and commercial commitments
The Company in the normal course of business enters into various services and supply agreements in connection with its clinical trials to ensure the supply of certain products and product lines during the Company’s clinical phase. These agreements often have minimum purchase commitments and generally terminate upon the termination of the clinical trial. Minimum purchase commitments under these agreements include individual commitments up to $1.7 million. Aggregate remaining minimum commitments amount to approximately $6.2 million with payments ranging from three to eight years or upon completion of the clinical trial, if earlier. The Company recorded research and development expenses in connection with these agreements of approximately $4.8 million and $11.3 million during the three and six months ended June 30, 2023, respectively (three and six months ended June 30, 2022 — $2.6 million and $4.3 million, respectively).
The Company also has supply agreements with third parties to purchase certain products for use in the Company’s full scale production process. The Company is committed to purchase a minimum quantity of product in the amount of approximately $111.9 million ($148.3 million CAD) over the contract term. The purchase commitments are contingent upon the completion of certain milestones by the third-party suppliers. The Company recorded $nil and $nil in connection with these agreements during the three and six months ended June 30, 2023, respectively (three and six months ended June 30, 2022 — $nil and $nil, respectively).
On May 10, 2023, the Company entered into an Irradiation Services Agreement (the "Irradiation Agreement") which expands the Company's reactor network. Pursuant to the Irradiation Agreement, the Company will receive irradiation services to irradiate ytterbium-176 (“176Yb”) and has minimum purchase commitments of approximately $32.4 million over the ten year contract term. During the three and six months ended June 30, 2023, the Company did not record any research and development expenses in connection with this agreement.
The Company also has an agreement with a third party to provide certain services in connection with the Company’s SPLASH clinical phase study. The agreement expires on the date of the completion or termination of the clinical trial. The remaining minimum purchase commitment under this agreement is approximately $24.0 million with payments that range from one to five years. The Company recorded research and development expenses in connection with this agreement of approximately $6.2 million and $11.1 million during the three and six months ended June 30, 2023, respectively (three and six months ended June 30, 2022 — $2.5 million and $5.6 million, respectively).
License agreements
The Company in the normal course of business enters into license and sublicense agreements in connection with its clinical trials and product development. For additional details of the Company’s license agreements, see Note 15 to the 2022 Financial Statements.
On April 17, 2023, POINT Biopharma Inc. entered into first and second amendments (the "Amendments") to that certain Sublicense Agreement, dated November 14, 2019, between POINT Biopharma Inc. and Scintomics GmbH ("Scintomics"). Pursuant to the Amendments, the exclusive, sublicensable, license is expanded to include all geographies worldwide and the Company will have increased flexibility in connection with sublicense arrangements.
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The Company recorded research and development expenses in connection to its license agreements of approximately $3.0 million and $3.5 million during the three and six months ended June 30, 2023, respectively (three and six months ended June 30, 2022 — $3.8 million and $4.6 million, respectively).
13. Net loss per share
Basic loss per share is computed by dividing the loss available to common stockholders by the weighted-average number of shares of Common Stock outstanding during the period. Diluted loss per share is computed by dividing loss available to common stockholders by the weighted-average number of shares of Common Stock outstanding during the period increased to include the number of additional shares of Common Stock that would have required adjustment or disclosurebeen outstanding if the potentially dilutive securities had been issued, using the treasury stock method.
Three months
ended
 June 30, 2023
Three months
ended
June 30, 2022
Six months
ended
 June 30, 2023
Six months
ended
June 30, 2022
Net loss attributable to common stockholders$25,410,839 $24,580,247 $41,941,510 $40,960,821 
Weighted-average common shares outstanding-basic and diluted105,724,215 90,124,295 105,692,615 90,123,288 
Net loss per share attributable to common stockholders-basic and diluted$0.24 $0.27 $0.40 $0.45 
The Company’s potentially dilutive securities, which include stock options, have been excluded from the computation of diluted net loss per share as the effect would be to reduce the net loss per share. The Company's PSU's are considered contingently issuable shares for the purpose of the computation of loss per share and have been excluded on the basis that as of June 30, 2023, the performance condition for vesting had not been achieved. Therefore, the weighted-average number of shares of Common Stock outstanding used to calculate both basic and diluted net loss per share attributable to the holders of Common Stock is the same.
14. Income Taxes
The Company calculates its interim tax provision at the end of each interim period and estimates the annual effective tax rate which is applied to its ordinary quarterly earnings. The computation of the annual estimated effective tax rate at each interim period requires certain estimates and significant judgment including, but not limited to, the expected operating income for the year, projections of the proportion of income earned and taxed in foreign jurisdictions, permanent and temporary differences between book and tax amounts, and the likelihood of recovering deferred tax assets generated in the current year. The accounting estimates used to compute the provision for income taxes may change as new events occur, additional information is obtained or as the tax environment changes.
The Company has operations in both the United States and Canada, and as such it is subject to tax in both countries. The income tax benefit and expense for the three months ended June 30, 2023 and June 30, 2022 was $921,298 and $183,405, respectively and the income tax benefit and expense for the six months ended June 30, 2023 and June 30, 2022 was $1,159,940 and $271,521, respectively. The income tax benefit for the three and six months ended June 30, 2023, consists primarily of tax benefits related to research and development tax credits partially offset by current taxes in Canada. The income tax expense for the three and six months ended June 30, 2022, consists of current taxes in Canada.
The Company files income tax returns in the U.S. federal, certain states, and Canada with varying statutes of limitations. The Company is not currently subject to tax examinations by any taxing jurisdiction. However, in the event of any such examination, there may or may not be an impact on the Company’s net operating loss carryforwards and credits. The Company does not anticipate that any potential tax adjustments resulting from such examinations would have a significant impact on its financial statements.

position or results of operations.

As of June 30, 2023, the Company believes no significant changes in the unrecognized tax benefits will occur within the next 12 months.
15. Related party transactions
The Company recognized expenses in connection with related party transactions in the unaudited interim condensed consolidated statements of operations as follows:
18

Three months ended
June 30, 2023
Three months ended
June 30, 2022
Six months
ended
 June 30, 2023
Six months
ended
June 30, 2022
Consulting fees on business activities to Board member$31,496 $102,396 $205,911 $169,092 
Reimbursement to Board member for occupancy costs17,894 17,898 35,313 35,676 
Total$49,390 $120,294 $241,224 $204,768 
Transactions with related parties are in the normal course of operations and have been measured at their agreed upon exchange amount.
During the three and six-month periods ended June 30, 2023 and 2022, the Company received consulting services for research and development from a Board member. As of June 30, 2023, $33,471 is recorded within accrued liabilities in relation to this consulting arrangement.
The Company currently has a lease arrangement in place with a Board member for the use of office space. The arrangement does not have a defined contractual lease term and is payable monthly. The Company has applied the short-term lease exemption under ASC 842 to this arrangement and is recording the lease payments of approximately $6,000 monthly as rent expense.
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Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations.

References to the “Company,” “our,” “us” or “we” refer to Therapeutics Acquisition Corp d/b/a Research Alliance Corp. I.

ITEM 2 – MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

The following discussion and analysis of the Company’sour financial condition and results of operations should be read in conjunctiontogether with theour unaudited interim condensed consolidated financial statements and the notes thereto containedfor the three and six months ended June 30, 2023 (the “Q2 2023 Financial Statements”) appearing elsewhere in this report. Certain informationQuarterly Report on Form 10-Q and our audited consolidated financial statements and notes thereto for the periods ended December 31, 2022 and 2021 (the “2022 Financial Statements”) contained in our Annual Report on Form 10-K for the discussionfiscal year ended December 31, 2022, as filed with the Securities and analysis set forth below includes forward-looking statements that involve risks and uncertainties.

Exchange Commission ("SEC") on March 27, 2023 (the "2022 Form 10-K"). Please also see the section entitled “Cautionary Note Regarding Forward-Looking Statements.”

Cautionary Note Regarding Forward-Looking Statements

This Quarterly Report on Form 10-Q includes forward-looking statements withincontains “forward-looking statements” which are made pursuant to the meaningsafe harbor provisions of Section 27A of the Securities Act of 1933, as amended, (the “Securities Act”), and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”). We have based theseOur forward-looking statements on our current expectations and projections about future events. These forward-looking statements are subject to known and unknown risks, uncertainties and assumptions about us that may cause our actual results, levels of activity, performance or achievements to be materially different from any future results, levels of activity, performance or achievements expressed or implied by such forward-looking statements. In some cases, you can identify forward-looking statements by terminology such as “may,” “should,” “could,” “would,” “expect,” “plan,” “anticipate,” “believe,” “estimate,” “continue,” or the negative of such terms or other similar expressions. Such statements include, but are not limited to, statements regarding our or our management team’s expectations, hopes, beliefs, intentions or strategies regarding the future. In addition, any statements that refer to projections, forecasts or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking statements. The words “anticipate,” “believe,” “contemplate,” “continue,” “could,” “estimate,” “expect,” “intends,” “may,” “might,” “plan,” “possible business combinations,” “potential,” “predict,” “project,” “should,” “will,” “would” and similar expressions (including the negative of any of the foregoing) may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. By their nature, forward-looking statements involve risks and uncertainties because they relate to events and depend on circumstances that may or may not occur in the future. These factors include, but not limited to, the following:

the success, cost and timing of our product development activities and clinical trials, our plans for clinical development of our product candidates and the financing thereof,initiation and completion of any other clinical trials and related matters, as well as allpreparatory work and the expected timing of the availability of results of the clinical trials;
our ability to recruit and enroll suitable patients in our clinical trials;
the potential attributes and benefits of our product candidates;
our ability to obtain and maintain regulatory approval for our product candidates, and any related restrictions, limitations or warnings in the label of an approved product candidate;
our ability to obtain funding for our operations, including funding necessary to complete further development, approval and, if approved, commercialization of our product candidates;
the period over which we anticipate our existing cash and cash equivalents will be sufficient to fund our operating expenses and capital expenditure requirements;
the potential for our business development efforts to maximize the potential value of our portfolio;
our ability to identify, in-license or acquire additional product candidates;
our ability to maintain the license agreements underlying our product candidates;
our ability to compete with other companies currently marketing or engaged in the development of treatments for the indications that we are pursuing for our product candidates;
our expectations regarding our ability to obtain and maintain intellectual property protection for our product candidates and the duration of such protection;
our ability to contract with and rely on third parties to assist in conducting our clinical trials and manufacture our product candidates;
the development and expansion of our own manufacturing facility in Indianapolis, Indiana and the ability of this facility to provide adequate production capacity to meet future clinical and commercial demands for our product candidates;
the size and growth potential of the markets for our product candidates, and our ability to serve those markets, either alone or in partnership with others;
the rate and degree of market acceptance of our product candidates, if approved;
the pricing and reimbursement of our product candidates, if approved;
regulatory developments in the United States and foreign countries;
the impact of laws and regulations;
our ability to attract and retain key scientific, medical, commercial or management personnel;
our estimates regarding expenses, future revenue, capital requirements and needs for additional financing;
our financial performance;
the level of activity in the trading market for our common stock, par value $0.0001 per share ("Common Stock") and the volatility of the market price of our Common Stock;
the effect of the COVID-19 pandemic, the Russo-Ukrainian conflict and/or bank failures on the foregoing; and
other factors detailed under the section entitled “Risk Factors” in the 2022 Form 10-K.
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These forward-looking statements are based on current expectations and beliefs concerning future developments and their potential effects. There can be no assurance that future developments affecting us will be those that we have anticipated. These forward-looking statements involve a number of risks, uncertainties (some of which are beyond our control) or other than statements of historical fact included in this Form 10-Q. Factorsassumptions that mightmay cause actual results or contributeperformance to such a discrepancybe materially different from those expressed or implied by these forward-looking statements. These risks and uncertainties include, but are not limited to, those factors described under the heading “Risk Factors” in the 2022 Form 10-K. Should one or more of these risks or uncertainties materialize, or should any of our other Securitiesassumptions prove incorrect, actual results may vary in material respects from those projected in these forward-looking statements. Some of these risks and Exchange Commission (“SEC”) filings.

uncertainties may in the future be amplified by the COVID-19 outbreak, the Russo-Ukrainian conflict and/or adverse developments affecting the financial services industry and there may be additional risks that we consider immaterial or which are unknown. It is not possible to predict or identify all such risks. Readers are cautioned not to place undue reliance on forward-looking statements because of the risks and uncertainties related to them and to the risk factors. We do not undertake any obligation to update or revise any forward-looking statements, which speak only as of the date made, whether as a result of new information, future events or otherwise, except as may be required under applicable securities laws.

Overview

Introduction
We are a blank checkglobally focused radioligand company building a platform for the clinical development and commercialization of radioligands that fight cancer. We have a pipeline of product candidates and early-stage development programs, in-house manufacturing capabilities, and a secured supply for rare medical isotopes like actinium-225 ("225Ac") and lutetium-177 ("177Lu").

Our team brings decades of combined experience in radioligand clinical development and manufacturing. In a space where manufacturing is often overlooked, the Company has unique capabilities. In addition to our Center of Radioligand Excellence (CORE), a commercial-scale radioligand production campus in Indianapolis, Indiana, we also operate the POINT Institute for Radioligand Innovation (PIRI) in Toronto, Ontario, a state of the art GMP R&D center focused on bringing novel programs from discovery to the clinic. Furthermore, management has leveraged their prior relationships to assemble resilient radioisotope supply chains, which even includes processing our own no-carrier-added ("n.c.a") 177Lu isotope in-house.

Our predecessor was incorporated on April 15, 2020September 18, 2019 as POINT Theranostics Inc. under the DGCL and subsequently amended its name to “POINT Biopharma Inc.” on November 22, 2019. POINT Biopharma Inc. became a Delaware corporationwholly-owned subsidiary of POINT Biopharma Global Inc. (together with its consolidated subsidiaries, “POINT” or the “Company”) pursuant to a merger on June 30, 2021.

Recent Developments
PNT2002: 177Lu-based PSMA-targeted radiopharmaceutical

Enrollment in PNT2002's phase 3 Study evaluating metastatic castration-resistant Prostate cancer using 177Lu-PNT2002 PSMA therapy After Second-line Hormonal treatment (“SPLASH") trial (NCT04647526) is complete and top line data is expected in the fourth quarter of 2023. Six trial sites remain open for recruitment to complete a separate pharmacokinetic sub-study. POINT is not experiencing any supply constraints or shortages related to its lutetium-177-labeled programs.

PNT2004:fibroblast activation protein-alpha (FAP-alpha) inhibitor

In May 2023, enrollment in cohort 3 of the phase 1 FAPi Radioligand OpeN-Label, phase 1 study to evaluate safety, Tolerability and dosImetry of 177Lu-PNT6555; a dose Escalation study for tReatment of patients with select solid tumors, ("FRONTIER") trial (NCT05432193) began, and a total of seven participants have been dosed with 177Lu-PNT6555 to date. We continue to anticipate data from the full FRONTIER study to be available in the first half of 2024.

In June 2023, a Trial-in-Progress poster for FRONTIER was presented at the 2023 American Society of Clinical Oncology (ASCO) Annual Meeting, which included trial background information, study design considerations, and a cohort enrollment status update.

Later in June 2023, we published and presented preclinical data at the 2023 Annual Meeting of the Society of Nuclear Medicine & Molecular Imaging (SNMMI). The auger electron and beta emitting isotope terbium-161 was paired with POINT’s FAP-targeted PNT6555 ligand and showed robust anti-tumor efficacy, similar to 225Ac-PNT6555 and 177Lu-
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PNT6555. Also, preclinical proof-of-concept was established for synergistic interaction of immuno- and radioligand therapies with 177Lu-PNT6555.

PNT2001: 225Ac-labelled next-generation PSMA-targeted radiopharmaceutical

At our virtual Investor Day in June 2023, we unveiled the trial design for the purposephase 1 portion of effectingACCEL, the first-in-human phase 1/2 clinical trial for PNT2001's actinium-225 program. The trial was designed to enable the parallel exploration of PNT2001 in two patient populations: later-stage mCRPC patients and earlier-stage BCR or Prostate-Specific Membrane Antigen ("PSMA")-positive oligorecurrent patients. We anticipate a merger,health authority submission in the fourth quarter of 2023, and expect the first patient dosed in this trial to be in the first quarter of 2024.

Manufacturing & Supply Chain Updates

In April 2023, we announced an agreement for the supply of actinium-225 with Eckert & Ziegler. Eckert & Ziegler will provide predetermined amounts of GMP grade actinium-225 to POINT for use in the development of POINT’s pipeline of next generation actinium-225-based radioligands.

In May 2023, we announced a collaboration to create Ionetix Alpha Corp. (Ionetix-α). Ionetix-α, a new subsidiary of IONETIX Corp., is focused on near-term, commercial-scale production of GMP grade therapeutic isotopes, such as actinium-225. IONETIX has transferred its alpha therapy isotope business assets into Ionetix-α. POINT will invest $10 million into Ionetix-α.

In June 2023, we announced the intent to collaborate with AdvanCell, an Australian clinical stage radiopharmaceutical company, for the development of a global lead-212 radioisotope and radioligand supply chain and drug manufacturing network to specifically support the clinical development and commercialization of lead-212-labeled radioligands by each company.

Risks & Liquidity

Drug research and development is very expensive and involves a high degree of risk. Only a small number of research and development programs result in the commercialization of a product. We will not generate revenue from product sales unless and until we successfully complete clinical development of, are able to obtain regulatory approval for and successfully commercialize, the product candidates we are currently developing or may develop. We currently do not have any product candidates approved for commercial sale.

Our product candidates, currently under development or that we may develop, will require significant additional research and development efforts, including extensive clinical testing and regulatory approval prior to commercialization. These efforts require significant amounts of additional capital, stock exchange, asset acquisition, stock purchase, reorganization,adequate personnel infrastructure and extensive compliance and reporting capabilities. There can be no assurance that our research and development activities will be successfully completed, that adequate protection for our licensed or similar business combination withdeveloped technology will be obtained and maintained, that products developed will obtain necessary regulatory approval or that any approved products will be commercially viable.
If we obtain regulatory approval for one or more businesses (the “Business Combination”). We have not selected any Business Combination target and we have not, nor has anyone on our behalf, initiated any substantive discussions, directly or indirectly, with any Business Combination target. We intend to effectuate our initial Business Combination using cash from the proceeds of our Initial Public Offering and the shares, our shares, debt or a combination of cash, equity, and debt.

The registration statement for our Initial Public Offering was declared effective on July 7, 2020. On July 10, 2020, we consummated the Initial Public Offering of 13,570,000 shares of Class A common stock at $10.00 per share, generating gross proceeds of $135.7 million, and incurring offering costs of approximately $8.1 million, inclusive of approximately $4.8 million in deferred underwriting commissions.

Simultaneously with the closing of the Initial Public Offering, we consummated the private sale of 471,400 shares of Class A Common Stock (the “Private Placement” or “Private Placement Shares”) at a price of $10.00 per Private Placement Share to our sponsor, Therapeutics Acquisition Holdings LLC (our “Sponsor”), generating gross proceeds of approximately $4.7 million.

Upon the closing of the Initial Public Offering and Private Placement, $135,700,000 ($10.00 per share) of the net proceeds of the Initial Public Offering and certain of the proceeds of the Private Placement were placed in a trust account (the “Trust Account”), located in the United States, at JP Morgan Chase Bank, N.A., maintained by Continental Stock Transfer & Trust Company, acting as trustee. Except with respect to interest earned on the funds in the trust account that may be released to us to pay our taxes, if any, the proceeds from the Initial Public Offering will not be released from the trust account until the earliest to occur of: (a) the completion of our initial Business Combination, (b) the redemption of any public shares properly tendered in connection with a stockholder vote to amend our amended and restated memorandum and articles of association (i) to modify the substance or timing of its obligation to redeem 100% of our public shares if we do not complete our initial Business Combination within 24 months from the closing of the Initial Public Offering or (ii) with respect to any other provisions relating to stockholders' rights or pre-initial Business Combination activity and (c) the redemption of all of our public shares if we have not completed our initial Business Combination within 24 months from the closing of the Initial Public Offer, subject to applicable law.


If we are unable to complete a Business Combination within 24 months from the closing of the Initial Public Offering, or July 10, 2022 (the "Combination Period"), we will (i) cease all operations except for the purpose of winding up, (ii) as promptly as reasonably possible but not more than ten business days thereafter, redeem the Public Shares, at a per-share price, payable in cash, equal to the aggregate amount then on deposit in the Trust Account including interest earned on the funds held in the Trust Account and not previously released to us to pay our income taxes (less up to $100,000 of interest to pay dissolution expenses), divided by the number of then outstanding Public Shares, which redemption will completely extinguish Stockholders' rights as stockholders (including the right to receive further liquidating distributions, if any), subject to applicable law, and (iii) as promptly as reasonably possible following such redemption, subject to the approval of our remaining stockholders and our board of directors, proceed to commence a voluntary liquidation and thereby a formal dissolution of the Company, subject in each case to our obligations to provide for claims of creditors and the requirements of other applicable law.

The issuance of additional shares in a Business Combination:

§ may significantly dilute the equity interest of investors in this offering, which dilution would increase if the anti-dilution provisions in the shares of Class B common stock resulted in the issuance of shares of Class A common stock on a greater than one-to-one basis upon conversion of the shares of Class B common stock;

§ may subordinate the rights of holders of shares of Class A common stock if shares of preferred stock are issued with rights senior to those afforded our shares of Class A common stock;

§ could cause a change in control if a substantial number of shares of our Class A common stock are issued, which may affect, among other things, our ability to use our net operating loss carry forwards, if any, and could result in the resignation or removal of our present officers and directors;

§ may have the effect of delaying or preventing a change of control of us by diluting the share ownership or voting rights of a person seeking to obtain control of us; and

§ may adversely affect prevailing market prices for our shares of Class A common stock. Similarly, if we issue debt securities or otherwise incur significant debt, it could result in:

§ default and foreclosure on our assets if our operating revenues after an initial Business Combination are insufficient to repay our debt obligations;

§ acceleration of our obligations to repay the indebtedness even if we make all principal and interest payments when due if we breach certain covenants that require the maintenance of certain financial ratios or reserves (in the absence of a waiver or renegotiation of that covenant);

§ our immediate payment of all principal and accrued interest, if any, if the debt security is payable on demand;

§ our inability to obtain necessary additional financing if the debt security contains covenants restricting our ability to obtain such financing while the debt security is outstanding;

§ our inability to pay dividends on our shares of Class A common stock;

§ using a substantial portion of our cash flow to pay principal and interest on our debt, which will reduce the funds available for dividends on our shares of Class A common stock if declared, expenses, capital expenditures, acquisitions and other general corporate purposes;


§ limitations on our flexibility in planning for and reacting to changes in our business and in the industry in which we operate;

§ increased vulnerability to adverse changes in general economic, industry and competitive conditions and adverse changes in government regulation; and

§ limitations on our ability to borrow additional amounts for expenses, capital expenditures, acquisitions, debt service requirements, execution of our strategy and other purposes and other disadvantages compared to our competitors who have less debt.

As indicated in the accompanying unaudited condensed financial statements, as of June 30, 2020, we had $0.1 million in cash and deferred offering costs of approximately $0.4 million. Further,product candidates, we expect to incur significant costsexpenses related to developing our commercialization capabilities to support product sales, marketing, and distribution activities, either alone or in collaboration with others. Prior to the Lantheus License Agreements, the Company had incurred significant net losses and had funded operations primarily through equity financings. Operating losses and negative cash flows were incurred during the three and six months ended June 30, 2023 and are expected to be incurred in the pursuitfuture.

In September 2022, POINT closed a previously announced underwritten public offering of approximately 15,500,000 shares of Common Stock at a public offering price of $9.00 per share (the "2022 Public Offering"). The gross proceeds to the Company from the 2022 Public Offering, before deducting underwriting discounts and commissions and other estimated offering expenses, were approximately $140.0 million. We believe that the net proceeds from the 2022 Public Offering and the Lantheus License Agreements, together with our available resources and existing cash, cash equivalents and investments, are sufficient to fund our operating expenses and capital expenditure requirements into 2026.
We are subject to risks and uncertainties common to early-stage companies in the biotechnology industry, including, but not limited to, successful discovery and development of our initial Business Combination. product candidates, development by competitors of new technological innovations, dependence on key personnel, the ability to attract and retain qualified employees, protection of proprietary technology, compliance with governmental regulations, the impact of COVID-19, the ability to secure additional capital to fund operations and commercial success of our product candidates. Product candidates currently under
22

development will require extensive preclinical and clinical testing and regulatory approval prior to commercialization. These efforts require significant amounts of additional capital, adequate personnel, infrastructure and extensive compliance-reporting capabilities. Even if our drug development efforts are successful, it is uncertain when, if ever, we will realize significant revenue from product sales.
We cannot assure youanticipate that our plansexpenses will increase significantly in connection with our ongoing activities, as we:
advance our clinical-stage product candidates 177Lu-PNT2002 and 177Lu-PNT6555 through clinical development;
advance our preclinical-stage product candidate 225Ac-PSMA-62, along with candidates developed with our CanSEEKTM Prodrug Platform, into clinical development;
seek to raise capitalidentify, acquire, and develop additional product candidates, including through business development efforts to invest in or in-license other technologies or product candidates;
hire additional clinical, quality control, medical, scientific, and other technical personnel to support our clinical operations;
expand our operational, financial and management systems and increase personnel to support our operations;
meet the requirements and demands of being a public company;
maintain, expand, and protect our intellectual property portfolio;
make milestone, royalty, or other payments due under various in-license or collaboration agreements;
seek regulatory approvals for any product candidates that successfully complete clinical trials; and
undertake any pre-commercialization activities to establish sales, marketing, and distribution capabilities for any product candidates for which we may receive regulatory approval in regions where we choose to commercialize our initial Business Combination willproducts on our own or jointly with third parties.
COVID-19 Pandemic, macroeconomic and other geopolitical events
Although the World Health Organization declared in early May of 2023 that COVID-19 no longer constitutes a public health emergency, the Company continues to actively monitor the COVID-19 developments and potential impact on the Company's employees, business and operations. The impact from global economic conditions and potential and continuing disruptions to and volatility in the credit and equity markets in the United States and worldwide are highly uncertain and cannot be successful.

Resultspredicted. The Company is currently operating in a period of Operationssignificant economic uncertainty, resulting from, among other things, the impact of the COVID-19 pandemic, geopolitical tensions, such as the ongoing military conflict between Russia and Known TrendsUkraine and heightened tensions between China and Taiwan, trade uncertainty, including changes in tariffs, sanctions, international treaties, and other trade restrictions, rising inflation and interest rates, and uncertainty and liquidity concerns in the broader financial services industry, including those caused by certain recent banking failures.


We are continuing to monitor the development and potential impact of these global economic and geopolitical events on our business and financial results. To date, we have not experienced any material business disruptions or Future Events

We have neither engagedincurred any impairment losses in any operations nor generated any revenues to date. Our only activities since inception have been organizational activities and those necessary to prepare for our Initial Public Offering. Following our Initial Public Offering, we will not generate any operating revenues until after completionthe carrying values of our initial Business Combination. We will generate non-operating income in the form of interest income on cash and cash equivalents after our Initial Public Offering. There has been no significant change in our financial or trading position and no material adverse change has occurred since the date of our audited financial statements. After our Initial Public Offering, we expect to incur increased expensesassets as a result of beingthese events and we are not aware of any specific related event or circumstance that would require us to revise our estimates reflected in the Q2 2023 Financial Statements. However, estimates and assumptions about future events and their effects cannot be determined with certainty and therefore require the exercise of judgment; as a public company (for legal, financial reporting, accounting,result, the Company’s estimates may change as new events occur and auditing compliance),additional information is obtained.

Components of Operating Results
See Item 7.“Management's Discussion and Analysis of Financial Condition and Results of Operations - Components of Operating Results” in our 2022 Form 10-K, for a discussion of the nature of our operating expense line items within our accompanying unaudited interim condensed consolidated statements of operations.
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Results of Operations - Three Months Ended June 30
The following table summarizes our results of operations for the three months ended June 30, 2023 and 2022:
For the three
months ended
June 30, 2023
For the three
months ended
June 30, 2022
Change
(In U.S. dollars)$$$%
Revenue
Other revenue4,865,856 — 4,865,856 100.0 %
Total revenue4,865,856  4,865,856 100.0 %
Operating expenses:    
Research and development31,276,573 20,813,882 10,462,691 50.3 %
General and administrative5,088,403 4,080,401 1,008,002 24.7 %
Total operating expenses36,364,976 24,894,283 11,470,693 46.1 %
Loss from operations(31,499,120)(24,894,283)(6,604,837)26.5 %
Other income (expenses):
Investment income5,335,753 509,700 4,826,053 946.8 %
Foreign currency loss(168,770)(12,259)(156,511)1,276.7 %
Total other income (expenses)5,166,983 497,441 4,669,542 938.7 %
Loss before income taxes(26,332,137)(24,396,842)(1,935,295)7.9 %
Income tax benefit (provision)921,298 (183,405)1,104,703 602.3 %
Net loss(25,410,839)(24,580,247)(830,592)3.4 %
Research and Development
The following table summarizes the components of research and development expenses for the three months ended June 30, 2023 and 2022:
For the three
months ended
June 30, 2023
For the three
months ended
June 30, 2022
Change
(In U.S. dollars)$$$%
Clinical trials9,284,858 8,286,606 998,252 12.0 %
Salaries and benefits7,847,232 4,312,716 3,534,516 82.0 %
Contract manufacturing7,189,671 3,374,158 3,815,513 113.1 %
Depreciation and overhead3,548,091 975,241 2,572,850 263.8 %
Sponsored research & product licenses3,036,390 3,805,325 (768,935)(20.2)%
Regulatory consulting370,331 59,836 310,495 518.9 %
Total31,276,573 20,813,882 10,462,691 50.3 %

For the three months ended June 30, 2023, as wellcompared to the three months ended June 30, 2022, the increase in research and development expenses was primarily due to increases in (a) costs incurred in clinical trials and contract manufacturing as for due diligence expenses. We expect our expenseswe continue to increase substantially after the closingscale of our Initial Public Offering.

Liquiditytrials and Capital Resources

Our liquidity needs have been satisfied prioroperations, (b) personnel costs as the Company continues to expand its research and development headcount, most notably in our Indianapolis manufacturing facility and the completion of our Initial Public Offering through receipt of a $25,000 capital contribution from our Sponsor in exchange for the issuance of the Founder SharesPIRI, and (c) depreciation and overhead primarily related to our SponsorIndianapolis manufacturing facility. This was partially offset by decreased costs associated with our licensing agreements and a commitment from our Sponsor to loan us up to $300,000 to cover our expensesrelated sponsored research in connection with our Initial Public Offering. The net proceeds from (i)product candidates both preclinical and clinical. For the salethree months ended June 30, 2023, the Company incurred approximately $11.2 million and $1.4 million of direct costs associated with its PNT2002 and PNT2003 programs, respectively. These figures exclude amounts for salaries and benefits, depreciation and overhead costs which are not allocated by program.





24

General and administrative
General and administrative expenses increased for the sharesthree months ended June 30, 2023, as compared to the three months ended June 30, 2022, primarily in connection with increased headcount compared to the prior year period as the scale of Class A common stock in our Initial Public Offering, after deducting offering expensesoperations continues to increase.
Other Income (Expenses)
For the three months ended June 30, 2023 and 2022, other income (expenses) consist mainly of $0.6 million, underwriting commissions of $2.7 million (excluding deferred underwriting commissions of $4.8 million), and (ii) the sale of the Private Placement Shares for a purchase price of $4.7 million will be $137.1 million. $135.7 million will be held in the Trust Account, which includes the deferred underwriting commissions described above. The proceeds held in the Trust Account will be invested only in U.S. government treasury obligations with a maturity of 185 days or less or in money market funds meeting certain conditions under Rule 2a-7 under the Investment Company Act which invest only in direct U.S. government treasury obligations. The remaining $1.3 million will not be held in the Trust Account.

We intend to use substantially all of the funds held in the Trust Account, including any amounts representing interest earned on the Trust Account (less taxes payable and deferred underwriting commissions), to complete our initial Business Combination. We may withdraw interest income to pay our income taxes, if any. Our annual income tax obligations will depend on the amount of(a) interest and other income earned on the amounts heldCompany's cash, cash equivalents and investments, partially offset by (b) a foreign exchange loss primarily associated with foreign currency transactions occurring within the Company’s Canadian subsidiary. The increase in the Trust Account. We expectcurrent period reflects the increase in investments primarily in connection with cash received in connection with equity financings and the Lantheus License Agreements.

Income Tax Benefit (Provision)
For the three months ended June 30, 2023, income tax benefit consists primarily of estimated research and development tax credits available for carryback. This is partially offset by taxes owing in Canada in relation to taxable income generated through management and research and development services performed by the Canadian subsidiary of the Company. For the three months ended June 30, 2022, income tax expense consisted primarily of taxes owing in Canada in relation to taxable income generated through management and research and development services performed by the Canadian subsidiary of the Company.
Results of Operations - Six Months Ended June 30
The following table summarizes our results of operations for the six months ended June 30, 2023 and 2022:
For the six
months ended
June 30, 2023
For the six
months ended
June 30, 2022
Change
(In U.S. dollars)$$$%
Revenue
Other revenue14,323,120 — 14,323,120 100.0 %
Total revenue14,323,120  14,323,120 100.0 %
Operating expenses:   
Research and development58,187,045 33,314,730 24,872,315 74.7 %
General and administrative10,098,532 7,888,343 2,210,189 28.0 %
Total operating expenses68,285,577 41,203,073 27,082,504 65.7 %
Loss from operations(53,962,457)(41,203,073)(12,759,384)31.0 %
Other income (expenses):
Investment income11,099,967 557,673 10,542,294 1,890.4 %
Foreign currency loss(238,960)(43,900)(195,060)444.3 %
Total other income (expenses)10,861,007 513,773 10,347,234 2,014.0 %
Loss before income taxes(43,101,450)(40,689,300)(2,412,150)5.9 %
Income tax benefit (provision)1,159,940 (271,521)1,431,461 527.2 %
Net loss(41,941,510)(40,960,821)(980,689)2.4 %
Research and Development
The following table summarizes the components of research and development expenses for the six months ended June 30, 2023 and 2022:
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For the six
months ended
June 30, 2023
For the six
months ended
June 30, 2022
Change
(In U.S. dollars)$$$%
Clinical trials18,173,278 13,015,747 5,157,531 39.6 %
Salaries and benefits14,491,043 8,051,246 6,439,797 80.0 %
Contract manufacturing15,422,020 6,083,741 9,338,279 153.5 %
Depreciation and overhead5,897,604 1,483,462 4,414,142 297.6 %
Sponsored research & product licenses3,536,390 4,555,325 (1,018,935)(22.4)%
Regulatory consulting666,710 125,209 541,501 432.5 %
Total58,187,045 33,314,730 24,872,315 74.7 %

For the six months ended June 30, 2023, as compared to the six months ended June 30, 2022, the increase in research and development expenses was due to the same or substantially same factors as noted above for the three months ended June 30, 2023. For the six months ended June 30, 2023, the Company incurred approximately $22.7 million and $2.6 million of direct costs associated with its PNT2002 and PNT2003 programs, respectively. These figures exclude amounts for salaries and benefits, depreciation and overhead costs which are not allocated by program.

General and administrative
General and administrative expenses increased for the six months ended June 30, 2023, as compared to the six months ended June 30, 2022, due to the same or substantially same factors as noted above for the three months ended June 30, 2023.
Other Income (Expenses)
For the six months ended June 30, 2023 and 2022, other income (expenses) consist mainly of (a) interest and other income earned on the amountCompany's cash, cash equivalents and investments, partially offset by (b) a foreign exchange loss primarily associated with foreign currency transactions occurring within the Company’s Canadian subsidiary. The increase in the Trust Account (if any)current period reflects the same or substantially same factors as noted above for the three months ended June 30, 2023.
Income Tax Benefit (Provision)
For the six months ended June 30, 2023, income tax benefit consists primarily of estimated research and development tax credits available for carryback. This is partially offset by taxes owing in Canada in relation to taxable income generated through management and research and development services performed by the Canadian subsidiary of the Company. For the six months ended June 30, 2022, income tax expense consisted primarily of taxes owing in Canada in relation to taxable income generated through management and research and development services performed by the Canadian subsidiary of the Company.
Liquidity and Capital Resources
Sources of Liquidity and Capital
Except for the upfront payment received pursuant to the Lantheus License Agreements, the Company has incurred significant net losses and funded operations primarily through equity financings. Operating losses and negative cash flows were incurred in the three and six months ended June 30, 2023 and are expected to be incurred in future periods. We are subject to risks and uncertainties common to early-stage companies in the biotechnology industry. Product candidates currently under development will require extensive preclinical and clinical testing and regulatory approval prior to commercialization. These efforts require significant amounts of additional capital, adequate personnel, and infrastructure and extensive compliance-reporting capabilities. Even if our drug development efforts are successful, it is uncertain when, if ever, we will realize significant revenue from product sales.

Net losses totaled $25.4 million and $24.6 million for the three months ended June 30, 2023 and 2022 and $41.9 million and $41.0 million for the six months ended June 30, 2023 and 2022, respectively.
In connection with the 2022 Public Offering, on September 16, 2022, we issued 13,900,000 shares of Common Stock resulting in net proceeds of approximately $117.3 million, excluding certain transaction costs incurred in connection with filing the S-3 (defined below) and on October 3, 2022, we issued an additional 1,589,779 shares of Common Stock for net
26

proceeds to the Company of approximately $13.4 million as a result of underwriters exercising their option to purchase additional shares pursuant to the underwriting agreement. On December 22, 2022, we received $260.0 million in connection with the Lantheus License Agreements. We intend to use the net proceeds from these transactions to fulfill our obligations under the Lantheus License Agreements, for general corporate purposes, funding of development programs, payment of milestones pursuant to our license agreements, general and administrative expenses, licensing of additional product candidates, and supporting our working capital needs.
Future Funding Requirements
Our primary use of cash is to fund operating expenses, primarily related to our research and development activities. Cash used to fund operating expenses is impacted by the timing of when we pay these expenses, as reflected in the change in our outstanding accounts payable, accrued expenses and prepaid expenses.
Operating losses and negative cash flows are expected to continue to be incurred in the future. We may require additional capital to meet operational needs and capital requirements for clinical trials, for other research and development expenditures, and for business development activities. Because of the numerous risks and uncertainties associated with the development and commercialization of our product candidates, we are unable to estimate the amounts of increased capital outlays and operating expenditures associated with our current and anticipated clinical trials and preclinical studies.
Our future funding requirements will depend on many factors, including, but not limited to:
the scope, progress, results and costs of researching and developing our current product candidates, as well as other additional product candidates we may develop and pursue in the future;
the timing of, and the costs involved in, obtaining regulatory and marketing approvals for our product candidates and any other additional product candidates we may develop and pursue in the future;
the number of future product candidates that we may pursue and their development requirements;
subject to receipt of regulatory approval, if any, the costs of commercialization activities for our product candidates, to the extent such costs are not the responsibility of any future collaborators, including the costs and timing of establishing product sales, marketing, distribution, and manufacturing capabilities;
subject to receipt of regulatory approval, revenue, if any, received from commercial sales of our product candidates or any other additional product candidates we may develop and pursue in the future;
the achievement of milestones that trigger payments under our various license agreements;
the extent to which we in-license or acquire rights to other products, product candidates or technologies;
our ability to establish collaboration arrangements for the development of our product candidates on favorable terms, if at all;
our headcount growth and associated costs as we expand our research and development and establish a commercial infrastructure;
the costs of preparing, filing and prosecuting patent applications, and maintaining and protecting our intellectual property rights, including enforcing and defending intellectual property related claims; and
the costs of operating as a public company.
As of June 30, 2023, we had cash, cash equivalents and investments of approximately $434.8 million, which is anticipated to fund operations into 2026. We have based this estimate on current assumptions that may change or prove to be wrong, which would cause us to utilize our available capital resources sooner than we expect. In addition, our cash, cash equivalents and investments are subject to the economic pressures or uncertainties associated with local or global economic recessions, and ongoing geopolitical events. The failure of one or more of the financial institutions in which our cash, cash equivalents or investments are held, any resulting inability for us to obtain the return of our funds from any of those financial institutions, or any other adverse condition suffered by those financial institutions, could impact access to our cash, cash equivalents or investments and could adversely impact our operating liquidity and financial performance.
On July 11, 2022 the SEC declared effective our shelf registration statement on Form S-3 (the “S-3”) that allows the Company to offer and sell to the public up to $400.0 million of our Common Stock, preferred stock, debt securities, warrants to purchase our Common Stock, preferred stock or debt securities, subscription rights to purchase our Common Stock, preferred stock or debt securities and/or units consisting of some or all of these securities, from time to time in one or more offerings. The details of any future offerings, along with the use of proceeds from any securities offered, will be sufficientdescribed in a prospectus supplement or other offering materials, at the time of offering. Also covered under the S-3 as part of the $400.0 million total amount is an at-the-market offering (“ATM”) of up to pay$150.0 million of our income taxes.Common Stock
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pursuant to a distribution agreement with Piper Sandler & Co. No shares of Common Stock were issued in connection with the ATM as of June 30, 2023. Pursuant to the S-3 and in connection with the 2022 Public Offering, on September 16, 2022 we issued 13,900,000 shares of Common Stock at the price of $9.00 per share, or an aggregate of $125.1 million, resulting in net proceeds of approximately $117.3 million, excluding certain transaction costs incurred in connection with filing the S-3, and on October 3, 2022, we issued an additional 1,589,779 shares of Common Stock at a public offering price of $9.00 per share for net proceeds to the Company of approximately $13.4 million as a result of an underwriters exercising their option to purchase additional shares pursuant to the underwriting agreement.

Until such time as we can generate substantial product revenue, if ever, we expect to finance our operations through a combination of equity offerings, debt financings, collaborations, strategic alliances and marketing, distribution or licensing arrangements. To the extent that ourwe raise additional capital through the sale of equity or convertible debt is used, in whole or in part, as consideration to completesecurities, our initial Business Combination, the remaining proceeds held in the trust accountstockholders' ownership interest will be used as working capital to financediluted, and the operationsterms of the target businessthese securities may include liquidation or businesses, make other acquisitions and pursue our growth strategies.

Prior to the completionpreferences that adversely affect rights of our initial Business Combination,stockholders. Debt financing and preferred equity financing, if available, may involve agreements that include covenants limiting or restricting our ability to take specific actions, such as incurring additional debt, making acquisitions or capital expenditures or declaring dividends. If we will have available to us the $1.3 million of proceeds held outside the trust account, as well as certain funds that can be made available to us through loans from our Sponsor. We will use these funds to primarily identify and evaluate target businesses, perform business due diligence on prospective target businesses, travel to and from the offices, plants or similar locations of prospective target businesses or their representatives or owners, review corporate documents and material agreements of prospective target businesses, and structure, negotiate and complete a Business Combination.


We do not believe we will need to raise additional funds following our Initial Public Offering in order to meet the expenditures required for operating our business prior to our initial Business Combination, other than funds available from loans from our Sponsor. However, if our estimates of the costs of identifying a target business, undertaking in-depth due diligence and negotiating an initial Business Combination are less than the actual amount necessary to do so,through collaborations, strategic alliances or marketing, distribution or licensing arrangements with third parties, we may have insufficient funds available to operate our business priorrelinquish valuable rights to our initial Business Combination. In order to fund working capital deficienciestechnologies, future revenue streams, research programs or finance transaction costs in connection with an intended initial Business Combination, our Sponsordrug candidates, or an affiliate of our Sponsor or certain of our officers and directors may, but are not obligated to, loan us funds as may be required. If we complete our initial Business Combination, we would repay such loaned amounts. In the event that our initial Business Combination does not close, we may use a portion of the working capital held outside the trust account to repay such loaned amounts but no proceeds from our trust account would be used for such repayment. Up to $1.5 million of such loans may be convertible into private placement shares at a price of $10.00 per share at the option of the lender. The terms of such loans, if any, have not been determined and no written agreements exist with respect to such loans. Prior to the completion of our initial Business Combination, we do not expect to seek loans from parties other than our Sponsor or an affiliate of our Sponsor as we do not believe third parties will be willing to loan such funds and provide a waiver against any and all rights to seek access to funds in our trust account.

We expect our primary liquidity requirements during that period to include approximately $350,000 for legal, accounting, due diligence, travel and other expenses associated with structuring, negotiating and documenting successful Business Combinations; $150,000 for legal and accounting fees related to regulatory reporting requirements; $100,000 for consulting, travel and miscellaneous expenses incurred during the search for an initial Business Combination target; $55,000 for Nasdaq continued listing fees; and $345,000 for general working capital that will be used for miscellaneous expenses and reserves. RA Capital will provide us office space and administrative and support services free of charge.

These amounts are estimates and may differ materially from our actual expenses. In addition, we could use a portion of the funds not being placed in trust to pay commitment fees for financing, fees to consultants to assist us with our search for a target business or as a down payment or to fund a "no-shop" provision (a provision designed to keep target businesses from "shopping" around for transactions with other companies or investorsgrant licenses on terms morethat may not be favorable to such target businesses) with respect to a particular proposed Business Combination, although we do not have any current intention to do so. If we entered into an agreement where we paid for the right to receive exclusivity from a target business, the amount that would be used as a down payment or to fund a "no-shop" provision would be determined based on the terms of the specific Business Combination and the amount of our available funds at the time. Our forfeiture of such funds (whether as a result of our breach or otherwise) could result in our not having sufficient funds to continue searching for, or conducting due diligence with respect to, prospective target businesses.

Moreover, we may need to obtain additional financing to complete our initial Business Combination, either because the transaction requires more cash than is available from the proceeds held in our trust account, or because we become obligated to redeem a significant number of our public shares upon completion of the Business Combination, in which case we may issue additional securities or incur debt in connection with such Business Combination.us. If we are unable to completeraise additional funds through equity or debt financings or other arrangements when needed, we may be required to delay, limit, reduce or terminate our initial Business Combination becauseresearch, product development or future commercialization efforts, or grant rights to develop and market product candidates that we do notwould otherwise prefer to develop and market ourselves.


Going Concern
We assess and determine our ability to continue as a going concern in accordance with the provisions of ASC Topic 205-40, Presentation of Financial Statements—Going Concern. We have sufficient funds availabledetermined that the Company will continue as a going concern, which contemplates the realization of assets and the settlement of liabilities and commitments in the normal course of business.
Working Capital
Working capital is defined as current assets less current liabilities.
The following table summarizes our total working capital and current assets and liabilities as of June 30, 2023 and December 31, 2022:
As of
June 30,
2023
As of
December 31,
2022
Change
(In U.S. dollars)$$$%
Current assets432,375,303 530,822,730 (98,447,427)(18.5)%
Current liabilities41,155,794 79,738,440 (38,582,646)(48.4)%
Total working capital391,219,509 451,084,290 (59,864,781)(13.3)%
The decrease in working capital as of June 30, 2023, primarily reflects cash used for (a) operating expenses, including, personnel costs and research and development costs as we advance our clinical trials and continue to us, we will be forced to cease operationsexpand our pipeline, and liquidate the Trust Account.


Related Party Transactions

Founder Shares

On April 30, 2020,(b) capital expenditures for equipment and machinery used in our Sponsor paid $25,000manufacturing facility in consideration for 2,875,000 shares (the "Founder Shares") ofIndiana. This was partially offset by interest and other income earned on the Company's common stock, par value $0.0001 per share (the "common stock"). Incash, cash equivalents and investments. The decrease in current liabilities primarily reflects the payment of income taxes during the six months ended June 2020,30, 2023 of approximately $31.9 million, which had an equal and offsetting impact to current assets.

Cash Flows
The following table summarizes our Sponsor transferred 30,000 founder sharessources and uses of cash for the six months ended June 30, 2023 and 2022:
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For the six
months ended
June 30, 2023
For the six
months ended
June 30, 2022
Change
(In U.S. dollars)$$$%
Net cash flows used in operating activities(96,727,236)(31,068,981)(65,658,255)211.3 %
Net cash flows used in investing activities(132,606,078)(129,643,171)(2,962,907)2.3 %
Net cash flows provided by financing activities198,281 4,403 193,878 4403.3 %
Net decrease in cash and cash equivalents(229,135,033)(160,707,749)(68,427,284)42.6 %
Cash flows used in Operating Activities
Net cash flows used in operating activities represent the cash receipts and disbursements related to each of Messrs. Grau, Gray and Lubner.

We filed an Amended and Restated Certificate of Incorporation on June 15, 2020, such that we are authorized to issue shares of Class B common stock. Pursuant to the amendment, the Founder Shares were converted into shares of Class B common stock. On July 8, 2020, we effected a 1:1.18 stock split of our Class B common stock, resulting in our sponsor holding an aggregate of 3,286,300 founder shares and there being an aggregate of 3,392,500 founder shares outstanding.

The Founder Shares will automatically convert into shares of Class A common stock at the time of our initial Business Combination and are subject to certain transfer restrictions, as described in Note 6 of our unaudited condensed financial statements. Our Sponsor has agreed to forfeit up to 442,500 Founder Shares to the extent that the over-allotment option is not exercised in full by the underwriters. On July 10, 2020, the underwriters exercised the over-allotment option in full; thus, these Founder Shares are no longer subject to forfeiture.

Our Sponsor, directors and executive officers have agreed, subject to limited exceptions, not to transfer, assign or sell any of their Founder Shares or Private Placement Shares until the earlier to occur of: (A) one year after the completion of the initial Business Combination or (B) subsequent to the initial Business Combination, (x) if the last sale price of the shares of Class A common stock equals or exceeds $12.00 per share (as adjusted for share splits, share dividends, reorganizations, recapitalizations and the like) for any 20 trading days within any 30-trading day period commencing at least 150 days after the initial Business Combination, or (y) the date on which we complete a liquidation, merger, capital stock exchange or other similar transaction that results in all of our stockholders havingactivities other than investing and financing activities. Cash used in operating activities increased for the rightsix months ended June 30, 2023 compared to exchange their common stock forthe six months ended June 30, 2022 primarily due to a) continued advancement of our clinical trials and expansion of our pipeline, as described above and b) income taxes paid of approximately $31.9 million.

We believe that the net proceeds from the Lantheus License Agreements and the 2022 Public Offering, together with our available resources and existing cash securities or other property.

Private Placement Shares

Concurrently withand cash equivalents, are sufficient to fund our operating expenses and capital expenditure requirements into 2026.

Cash flows used in Investing Activities
For the closingsix months ended June 30, 2023 and 2022, net cash used in investing activities totaled $132.6 million and $129.6 million, respectively. The increase in cash used in investing activities relates to (a) the Company's investment of its available cash resources into fixed income investments, (b) purchase of the Initial Public Offering,Note Receivable from Ionetix-α and (c) increased capital expenditures for purchases in connection with our Sponsor purchased 471,400 Private Placement Shares, at a price of $10.00 per share in a private placement for an aggregate purchase price of $4.7 million. The Private Placement Shares are identical toIndianapolis manufacturing facility.
Cash flows provided by Financing Activities
For the shares of Class A common stock sold in the Initial Public Offering, subject to certain limited exceptions as described in Note 1 of our unaudited condensed financial statements.

The Sponsorsix months ended June 30, 2023 and our officers2022, net cash provided by financing activities totaled $198.3 thousand and directors have agreed, subject to limited exceptions, not to transfer, assign or sell any of their Private Placement Shares until 30 days after the completion$4 thousand, respectively, which consisted of the initial Business Combination.

Related Party Loans

On April 30, 2020,net proceeds received from the Sponsor agreed to loan us an aggregateexercise of up to $300,000 to cover expensesstock options and solely related to the Initial Public Offering pursuant to a promissory note (the "Note"). In May 2020, we borrowed $275,000 under the Note. The loansix months ended June 30, 2023, was non-interest bearing and the borrowings outstanding under the Note of $275,000 were repaid in full in July 2020.


In order to finance transaction costs in connection with a Business Combination, the Sponsor or an affiliate of the Sponsor, or certain of our officers and directors may, but are not obligated to, loan us funds as may be required ("Working Capital Loans"). If we complete a Business Combination, we would repay the Working Capital Loans out of the proceeds of the Trust Account released to us. Otherwise, the Working Capital Loans would be repaid only out of funds held outside the Trust Account. In the event that a Business Combination is not completed, we may use a portion of the proceeds held outside the Trust Account to repay the Working Capital Loans but no proceeds held in the Trust Account would be used to repay the Working Capital Loans. Except for the foregoing, the terms of such Working Capital Loans, if any, have not been determined and no written agreements exist with respect to such loans. The Working Capital Loans would either be repaid upon consummation of a Business Combination, without interest, or, at the lender's discretion, up to $1.5 million of such Working Capital Loans may be convertible into Private Placement Shares at a price of $10.00 per share.

Private Placement of Common Stock

The Sponsor has indicated an interest to purchase $25,000,000 of our common stock in a private placement that would occur concurrently with the consummation of the initial Business Combination. The funds from such private placement would be used as part of the consideration to the sellers in the initial Business Combination, and any excess funds from such private placement would be used for working capital in the post-transaction company. However, because indications of interest are not binding agreements or commitments to purchase, the Sponsor may determine not to purchase any such shares, or to purchase fewer shares than it indicated an interest in purchasing. Furthermore, we are not under any obligation to sell any such shares.

Commitments and Contingencies

Registration Rights

Holders of the Founder Shares will be entitled to registration rights with respect to the Founder Shares and Private Placement Shares (in the case of the Founder Shares, only after conversion of such shares into shares of Class A common stock) pursuant to a registration and stockholder rights agreement entered intopartially offset by payments made in connection with the consummationCompany's finance lease obligation.

Contractual Obligations and Other Commitments
The Company in the normal course of business enters into various services and supply agreements in connection with its clinical trials to ensure the Initial Public Offering. Holderssupply of certain product and product lines during the Founder SharesCompany’s clinical phase. These agreements often have minimum purchase commitments and Private Placement Shares are entitled to certain demand and "piggyback" registration and stockholder rights. However, the registration and stockholder rights agreement provides that we will not permit any registration statement filed under the Securities Act to become effective untilgenerally terminate upon the termination of the applicable lock-up period for the securities to be registered. We will bear the expenses incurred in connection with the filing of any such registration statements.

Underwriting Agreement

We granted the underwriters a 45-day option from the date of the final prospectus relatingclinical trial. For additional information, see Note 12 to the Initial Public OfferingQ2 2023 Financial Statements.

For additional information related to purchase up to 1,770,000 additional shares of Class A common stock to cover over-allotments, if any, at $10.00 per share, less underwriting discounts and commissions. The underwriters exercised this option in full on July 10, 2020.

The underwriters were entitled to an underwriting discount of $0.20 per share, or approximately $2.7 million in the aggregate, paid upon the closing of the Initial Public Offering. An additional fee of $0.35 per share, or approximately $4.8 million in the aggregate, will be payableour license agreements, please also see Note 12 to the underwriters for deferred underwriting commissions. The deferred underwriting commissions will become payableQ2 2023 Financial Statements and Notes 14 and 15 to the underwriters from the amounts held in the Trust Account solely in the event that we complete a Business Combination, subject to the terms of the underwriting agreement.

2022 Financial Statements.

Off-balance sheet arrangements

Risks and Uncertainties

Management continues to evaluate the impact of the COVID-19 pandemic on the industry and has concluded that while it is reasonably possible that the virus could have a negative effect on the our financial position, results of our operations and/or search for a target company, the specific impact is not readily determinable as of the date of these financial statements. The financial statements

We do not include any adjustments that might result from the outcome of this uncertainty.

Off-Balance Sheet Arrangements

As of June 30, 2020, we did not have any off-balance sheet arrangements or holdings in any variable interest entities.

Critical Accounting Policies and Estimates
This management’s discussion and analysis of our financial condition and results of operations is based on our Q2 2023 Financial Statements, which have been prepared in accordance with generally accepted accounting principles in the United States (“GAAP”) and include the accounts of the Company and its wholly-owned subsidiaries, POINT Biopharma Inc., POINT Biopharma Corp., POINT Biopharma USA, Inc. and West 78th Street, LLC, for financial information and pursuant to the rules and regulations of the SEC.
The preparation of the Q2 2023 Financial Statements in conformity with GAAP requires us to make estimates, judgments and assumptions that may affect the reported amounts of assets and liabilities, the disclosure of contingent assets and liabilities as definedof the date of the Q2 2023 Financial Statements and the reported amounts of expenses during the reporting
29

periods. Our estimates are based on our historical experience and on various other factors that we believe are reasonable under the circumstances, the results of which form the basis for making judgments about the carrying value of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates under different assumptions or conditions.
There have been no significant changes to our critical accounting policies and estimates from the information provided in Item 303(a)(4)(ii)7 “Management’s Discussion and Analysis of Regulation S-K.

JOBS Act

Financial Condition and Results of Operations,” in our 2022 Form 10-K except as below:


Leases
The JOBS ActCompany accounts for leases in accordance with ASC Topic 842, Leases ("ASC 842"). At the inception of an arrangement, we determine whether the arrangement is or contains provisions that, among other things, relax certain reporting requirements for qualifying public companies. We qualify as an "emerging growth company" and under the JOBS Act will be allowed to comply with new or revised accounting pronouncementsa lease based on the effective dateunique facts and circumstances present. The Company has elected not to recognize leases with an original term of one year or less on the consolidated balance sheets. We have also elected to account for private (not publicly traded) companies. We are electing to delay the adoption of new or revised accounting standards,lease and non-lease components as a result, we may not comply with new or revised accounting standardscombined lease component for our current lease portfolio. Right-of-use assets and lease liabilities are recognized at commencement date based on the relevant dates on which adoptionpresent value of such standards is required for non-emerging growth companies. Aslease payments over the lease term. Options to renew or early terminate a result, our financial statements may not be comparable to companies that comply with new or revised accounting pronouncements as of public company effective dates.

Additionally, welease are included in the processinitial lease term of evaluatinga lease when there is reasonable certainty that the benefits of relying onoption will be applied.


ASC 842 requires a lessee to discount its unpaid lease payments using the other reduced reporting requirements provided by the JOBS Act. Subject to certain conditions set forthinterest rate implicit in the JOBS Act,lease or, if as an "emerging growth company," we choose to rely on such exemptions we may notthat rate cannot be required to, among other things, (i) provide an auditor's attestation report on our system of internal controls over financial reporting pursuant to Section 404, (ii) provide all ofreadily determined, its incremental borrowing rate. The Company's incremental borrowing rate is determined using a secured borrowing rate for the compensation disclosure that may be required of non-emerging growth public companies under the Dodd-Frank Wall Street Reformsame currency and Consumer Protection Act, (iii) comply with any requirement that may be adopted by the PCAOB regarding mandatory audit firm rotation or a supplement to the auditor's report providing additional information about the audit and the financial statements (auditor discussion and analysis) and (iv) disclose certain executive compensation related items suchterm as the correlation between executive compensationassociated lease in a similar economic environment.

Lease expense for operating leases is recognized on a straight-line basis over the lease term and performanceincluded in operating expenses in the unaudited interim condensed consolidated statements of operations and comparisons of the CEO's compensationcomprehensive loss.
ITEM 3. – QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
Market risks relating to median employee compensation. These exemptions will apply for a period of five years following the completion of our initial public offering or until we are no longer an "emerging growth company," whichever is earlier.

Item 3.Quantitativeoperations result primarily from interest rate risk and Qualitative Disclosures about Market Risk.

foreign exchange risk. As of June 30, 2020, we2023, there were no material changes to our market risks from the information provided in Item 7A “Quantitative and Qualitative Disclosures About Market Risk” in our 2022 Form 10-K.


Inflation generally affects us by increasing our cost of labor and clinical trial costs. We do not subject to any marketbelieve that inflation had a material effect on our business, financial condition or interest rate risk. Followingresults of operations during the consummation of our Initial Public Offering, the net proceeds of our Initial Public Offeringthree and the sale of the Private Placement Shares are held in the Trust Account invested in U.S. government treasury obligations with a maturity of 185 days or less or in money market funds meeting certain conditions under Rule 2a-7 under the Investment Company Act which invest only in direct U.S. government treasury obligations. Due to the short-term nature of these investments, we believe there will be no associated material exposure to interest rate risk.

Itemsix months ended June 30, 2023 and 2022.

ITEM 4.Controls and Procedures.

– CONTROLS AND PROCEDURES

Evaluation of Disclosure Controls and Procedures

Under the supervision and with the participation of our management, including our Chief Executive Officer and Chief Financial Officer, we conducted an evaluation of the effectiveness of our

We maintain disclosure controls and procedures as of the end of the fiscal quarter ended June 30, 2020, as such term is defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act. Based on this evaluation, our Chief Executive Officer and Chief Financial Officer have concluded that during the period covered by this report, our disclosure controls and procedures were effective.


Disclosure controls and procedures are designed to ensure that information required to be disclosed by us in ourthe reports that we file or submit under the Exchange Act reports is recorded, processed, summarized, and reported within the time periods specified in the SEC’s rules and forms,forms. Such disclosure controls and procedures include, without limitation, controls and procedures designed to ensure that such information required to be disclosed by us in reports that we file or submit under the Exchange Act is accumulated and communicated to our management, including our Chief Executive Officer and Chief Financial Officer, or persons performing similar functions, as appropriate to allow timely decisions regarding required disclosure.

As of June 30, 2023, our management, with the participation of our Chief Executive Officer and Chief Financial Officer, evaluated the effectiveness of our disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act). Our management recognizes that any controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving their objectives, and management necessarily applies its judgment in evaluating the cost-benefit relationship of possible controls and procedures.
Our Chief Executive Officer and Chief Financial Officer have concluded that, based on the evaluation described above, as of June 30, 2023, our disclosure controls and procedures were effective.
Changes in Internal Control over Financial Reporting

There was no change in our internal control over financial reporting that occurred during the fiscal quarter ended June 30, 2020 covered by this Quarterly Report on Form 10-Q2023 that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.

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PART II - OTHER INFORMATION

Item

ITEM 1. Legal Proceedings.

None.

Item – LEGAL PROCEEDINGS

From time to time, we may be subject to legal proceedings and claims in the ordinary course of business. We are not currently aware of any such proceedings or claims that we believe will have, individually or in the aggregate, a material adverse effect on our business, financial condition or results of operations.
ITEM 1A. Risk Factors.

– RISK FACTORS

Factors that could cause our actual results to differ materially from those described in this Quarterly Report on Form 10-Q are any of the risks and uncertainties described in our 2022 Form 10-K. If any of these risks are realized, our business, financial condition, operating results and prospects could be materially and adversely affected. Additional risks and uncertainties not presently known to us or that we currently deem immaterial also may impair our business operation.
As of the date of this Quarterly Report on Form 10-Q, there have been no material changes to the risk factorsrisks and uncertainties disclosed in our final prospectus filed with the SEC on July 7, 2020, except we2022 Form 10-K. We may disclose changes to such factors or disclose additional factors from time to time in our future filings with the SEC.

Item

ITEM 2. – UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS
Unregistered Sales of Equity Securities and Use
We did not have any unregistered sales of Proceeds from Registeredequity securities during the quarter ended June 30, 2023.

Issuer Purchases of Equity Securities

On July 10, 2020, we consummated

We did not repurchase any of our equity securities during the Initial Public Offering of 13,570,000 shares of Class A common stock, including the issuance of 1,770,000 shares as a resultquarter ended June 30, 2023.
ITEM 3. – DEFAULTS UPON SENIOR SECURITIES
None.
ITEM 4. – MINE SAFETY DISCLOSURES
Not applicable.
ITEM 5. – OTHER INFORMATION
None of the underwriters’ exercise in fullCompany’s directors or officers adopted, modified, or terminated a Rule 10b5-1 trading arrangement or a non-Rule 10b5-1 trading arrangement during the Company’s fiscal quarter ended June 30, 2023.
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ITEM 6. – EXHIBITS
The Class A common stock was sold at a pricefollowing exhibits are filed as part of $10.00 per share, generating total gross proceeds of $135,700,000. Jefferies LLC acted as the sole book-running manager of the Initial Public Offering. The securities in the offering were registered under the Securities Act on a registration statementthis Quarterly Report on Form S-1 (No. 333-239196). The Securities and Exchange Commission declared the registration statements effective on July 7, 2020. Our shares of Class A common stock began trading on The Nasdaq Capital Market under the ticker symbol “TXAC” on July 8, 2020.

Substantially concurrently with the closing of the Initial Public Offering, we completed the private sale of 471,400 shares of Class A common stock at a purchase price of $10.00 per Private Placement Share, to our Sponsor, generating gross proceeds to us of approximately $4,714,000. The Private Placement Shares are identical to the Class A Common Stock sold in the Initial Public Offering, except that, so long as they are held by the Sponsor and their permitted transferees: (i) they may not, subject to certain limited exceptions, be transferred, assigned or sold by the Sponsor until the earlier of (A) one year after the completion of our initial Business Combination or (B) subsequent to our initial Business Combination, the date on which we complete a liquidation, merger, capital stock exchange, reorganization or other similar transaction that results in all of our stockholders having the right to exchange their common stock for cash, securities or other property, and (ii) they are entitled to registration rights. Additionally, if the closing price of our common stock equals or exceeds $12.00 per share (as adjusted for stock splits, stock capitalizations, reorganizations, recapitalizations and the like) for any 20 trading days within any 30-trading day period commencing at least 150 days after our initial Business Combination, the Private Placement Shares will be released from the lock-up. In addition, the Sponsor has agreed to waive its redemption rights with respect to the Private Placement Shares in connection with (i) the consummation of our initial Business Combination, including, without limitation, any such rights available in the context of a stockholder vote to approve such Business Combination, or (ii) a stockholder vote to approve an amendment to our second amended and restated certificate of incorporation to modify the substance or timing of our obligation to redeem 100% of the shares of Class A common stock sold in our Initial Public Offering if we have not consummated a Business Combination within 24 months of the closing of our Initial Public Offering or with respect to any other material provisions relating to our stockholders’ rights or pre-initial Business Combination activity or in the context of a tender offer made by us to purchase the Initial Public Offering shares (although the Sponsor, shall be entitled to redemption and liquidation rights with respect to any Initial Public Offering shares it holds if the we fail to consummate a Business Combination within 24 months of the closing of the IPO).

A total of $135,700,000, comprised of the proceeds from the Initial Public Offering and the sale of the Private Placement Shares, were placed in a U.S.-based trust account at JP Morgan Chase Bank, N.A., maintained by Continental Stock Transfer & Trust Company, acting as trustee.

We paid a total of $2,714,000 in underwriting discounts and commissions and $588,042 for other costs and expenses related to the Initial Public Offering. In addition, the underwriters agreed to defer up to $4,749,500 in underwriting discounts and commissions.

10-Q.

Exhibit Index

For a description of the use of the proceeds generated in our Initial Public Offering, see Part I, Item 2 of this Form 10-Q.

Item 3.Defaults Upon Senior Securities.

None.

Item 4. Mine Safety Disclosures.

Not applicable.

Item 5. Other Information.

None.

Item 6. Exhibits.

Exhibit

Number

Description
Exhibit
Number
Description
1.13.1
3.12nd Amended and Restated Certificate of Incorporation (Incorporatedof POINT Biopharma Global Inc. (incorporated by reference to Exhibit 3.1 to the Registrant’s Current Report on Form 8-K filed by the Company on July 10, 2020)1, 2021).
3.2
10.110.1†
10.2*
10.210.3*#
10.4*‡
31.1*
10.3Private Placement Class A Common Stock Purchase Agreement, dated July 7, 2020 by and among the Company and Therapeutics Acquisition Holdings, LLC (Incorporated by reference to Exhibit 10.3 to the Registrant’s Current Report on Form 8-K filed on July 10, 2020).
10.4Private Placement Class A Common Stock Purchase Agreement, dated July 8, 2020 by and among the Company and Therapeutics Acquisition Holdings, LLC (Incorporated by reference to Exhibit 10.4 to the Registrant’s Current Report on Form 8-K filed on July 10, 2020).
10.5Letter Agreement, dated July 7, 2020, by and among the Company, its officers, its directors and Therapeutics Acquisition Holdings, LLC (Incorporated by reference to Exhibit 10.5 to the Registrant’s Current Report on Form 8-K filed on July 10, 2020).
31.1
31.2*
31.2
32*
32.1
32.2Certification ofand Chief Financial Officer Pursuantpursuant to 18 U.S.C. Section  1350, as Adopted Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.Rule 13a-14(b) or Rule 15d-14(b).
101.INS*
101.INSXBRL Instance Document
101.SCH*
101.SCHXBRL Taxonomy Extension Schema Document
101.CAL*
101.CALXBRL Taxonomy Extension Calculation Linkbase Document
101.DEF*
101.DEFXBRL Taxonomy Extension Definition Linkbase Document
101.LAB*
101.LABXBRL Taxonomy Extension Label Linkbase Document
101.PRE*
101.PREXBRL Taxonomy Extension Presentation Linkbase Document
104Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101)


*    Filed herewith.

†    Schedules and exhibits to this Exhibit omitted pursuant to Regulation S-K Item 601(a)(5). The Registrant agrees to furnish supplementally a copy of any omitted schedule or exhibit to the SEC upon request.
#    Certain confidential portions (indicated by brackets and asterisks) have been omitted from this exhibit.
‡    Indicates a management contract or any compensatory plan, contract or arrangement.
32

SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereuntothereunto duly authorized on this 20th day of August, 2020.

authorized.
THERAPEUTICS ACQUISITION CORP.
POINT BIOPHARMA GLOBAL INC.
Date: August 14, 2023By:/s/ Matthew Hammond
Name: Matthew Hammond
Title:By:/s/Joe McCann
Dr. Joe McCann, Ph.D.
Chief Executive Officer
(Principal Executive Officer)
By:/s/Bill Demers
Bill Demers
Chief Financial Officer
(Principal Financial Officer)


33