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

March 31, 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 – 105,693,356
shares outstanding as of May 10, 2023.

Therapeutics Acquisition Corp.

d/b/a Research Alliance Corp. I

Quarterly Report on Form 10-Q


Table of Contents

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 June 30, 2020– Three Months ended March 31, 2023 and March 31, 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 – FINANCIAL STATEMENTS
POINT Biopharma Global Inc.
Interim Condensed Consolidated Balance Sheets
(In U.S. dollars)
March 31, 2023
(Unaudited)December 31, 2022
$$
ASSETS  
Current assets  
Cash and cash equivalents111,139,617 286,428,371 
Short-term investments318,893,583 238,783,470 
Prepaid expenses and other current assets4,546,707 5,610,889 
Total current assets434,579,907 530,822,730 
Non-current assets
Long-term investments89,170,335 16,119,430 
Property, plant and equipment, net34,773,967 31,380,576 
Total non-current assets123,944,302 47,500,006 
Total assets558,524,209 578,322,736 
LIABILITIES & STOCKHOLDERS' EQUITY
Current liabilities
Accounts payable15,918,532 7,703,150 
Accrued liabilities16,615,066 19,094,454 
Deferred revenue16,518,934 23,242,290 
Income taxes payable28,795,306 29,698,546 
Total current liabilities77,847,838 79,738,440 
Long-term income taxes payable1,452,356 1,452,356 
Deferred revenue, net of current portion7,444,239 10,178,147 
Total liabilities86,744,433 91,368,943 
Commitments and contingencies (Note 11)
Stockholders’ equity
Common Stock, par value $0.0001 per share, 430,000,000 authorized, 105,682,677 and 105,649,741 issued and outstanding as of March 31, 2023 and December 31, 2022, respectively10,568 10,565 
Additional paid-in capital449,546,931 448,391,574 
Retained earnings22,477,834 39,008,505 
Accumulated other comprehensive loss(255,557)(456,851)
Total stockholders’ equity471,779,776 486,953,793 
Total liabilities and stockholders’ equity558,524,209 578,322,736 
See accompanying Notes to the Unaudited Interim Condensed Consolidated Financial Statements
1

POINT Biopharma Global Inc.
Unaudited Interim Condensed Consolidated Statements of Operations
(In U.S. dollars)
For the three months ended
March 31,
2023
March 31,
2022
$ $
Revenue
Other revenue9,457,264— 
Total revenue9,457,264 
Operating expenses 
Research and development26,910,472 12,500,848 
General and administrative5,010,129 3,807,942 
Total operating expenses31,920,601 16,308,790 
Loss from operations(22,463,337)(16,308,790)
Other income (expenses)
Investment income5,764,214 47,973 
Foreign currency loss(70,190)(31,641)
Total other income (expenses)5,694,024 16,332 
Loss before income taxes(16,769,313)(16,292,458)
Income tax benefit (provision)238,642 (88,116)
Net loss(16,530,671)(16,380,574)
Net loss per basic and diluted common share:
Basic and diluted net loss per common share$(0.16)$(0.18)
Basic and diluted weighted average common shares outstanding105,660,655 90,122,269 
See accompanying Notes to the Unaudited Interim Condensed Consolidated Financial Statements
2

POINT Biopharma Global Inc.
Unaudited Condensed Consolidated Statements of Comprehensive Loss
(In U.S. dollars)
For the three months ended
March 31,
2023
March 31,
2022
$ $
Net loss$(16,530,671)$(16,380,574)
Other comprehensive income, net of tax
Net unrealized gain on available-for-sale debt securities201,294 — 
Total comprehensive loss$(16,329,377)$(16,380,574)

See accompanying Notes to the Unaudited Interim Condensed Consolidated Financial Statements.

THERAPEUTICS ACQUISITION CORP.

d/b/a RESEARCH ALLIANCE CORP. I

Statements

3

POINT Biopharma Global Inc.
Unaudited Interim 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 Consolidated Statements of Stockholders’ Equity

(In U.S. dollars, except share amounts)
Common StockAdditional
Paid-in Capital
Retained EarningsAccumulated Other Comprehensive LossTotal Equity
Number Amount   
 # $ $ $$ $
Balance at December 31, 2022105,649,741 10,565 448,391,574 39,008,505 (456,851)486,953,793 
Issuance of shares of Common Stock in connection with stock option exercises32,936 145,861 — — 145,864 
Stock-based compensation— — 1,009,496 — — 1,009,496 
Net loss— — — (16,530,671)— (16,530,671)
Other comprehensive income, net of tax— — — — 201,294 201,294 
Balance at March 31, 2023105,682,677 10,568 449,546,931 22,477,834 (255,557)471,779,776 
Common StockAdditional
Paid-in
Capital
Accumulated
Deficit
Accumulated Other Comprehensive LossTotal Equity
Number Amount   
 # $ $ $$ $
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 

See accompanying Notes to 442,500 sharesthe 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 three months ended
March 31, 2023March 31, 2022
$$
Cash flows from operating activities  
Net loss:(16,530,671)(16,380,574)
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation on property, plant and equipment537,627 224,234 
Stock-based compensation expense1,009,496 440,450 
Amortization of premiums (accretion of discounts) on investments, net(3,159,749)— 
Changes in operating assets and liabilities
Prepaid expenses and other current assets1,064,182 (197,829)
Accounts payable7,744,626 3,920,227 
Accrued liabilities(2,414,883)1,424,963 
Deferred revenue(9,457,264)— 
Income taxes payable(903,240)77,925 
Change in accrued interest and dividends within investments(281,465)— 
Net cash used in operating activities(22,391,341)(10,490,604)
Cash flows from investing activities
Purchase of investments, net of sales and maturities(149,518,510)— 
Purchase of property, plant and equipment(3,524,767)(940,931)
Net cash used in investing activities(153,043,277)(940,931)
Cash flows from financing activities
Issuance of shares of Common Stock in connection with stock option exercises145,864 942 
Net cash provided by financing activities145,864 942 
Net decrease in cash and cash equivalents(175,288,754)(11,430,593)
Cash and cash equivalents, beginning of period286,428,371 238,815,991 
Cash and cash equivalents, end of period111,139,617 227,385,398 
Supplemental disclosure of cash flow information:
Cash paid for income taxes(660,786)(116)
Non-cash investment activities:
Purchase of property, plant and equipment recorded in accounts payable and accrued liabilities1,815,752 1,052,186 

See accompanying Notes to the Sponsor that were subject to forfeiture ifUnaudited Interim Condensed Consolidated Financial Statements
5


1. Nature of business
POINT Biopharma Global Inc., together with its consolidated subsidiaries ("POINT" or 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.

The accompanying notes are an integral part of these unaudited condensed financial statements.


THERAPEUTICS ACQUISITION CORP.

d/b/a RESEARCH ALLIANCE CORP. I

UNAUDITED 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 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.

The accompanying notes are an integral part of these unaudited condensed financial statements.


THERAPEUTICS ACQUISITION CORP.

d/b/a RESEARCH ALLIANCE CORP. I

UNAUDITED 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 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.

The accompanying notes are an integral part of these unaudited condensed financial statements.


THERAPEUTICS ACQUISITION CORP.

d/b/a RESEARCH ALLIANCE CORP. I

UNAUDITED 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 accompanying notes are an integral part of these unaudited condensed financial statements.


THERAPEUTICS ACQUISITION CORP.

d/b/a RESEARCH ALLIANCE CORP. I

NOTES TO UNAUDITED Condensed FINANCIAL STATEMENTS

1.Organization, Business Operations and Basis of Presentation

Therapeutics Acquisition Corp. d/b/a Research Alliance Corp. I (the "Company"“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 available 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 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 years ended December 31, 2022 and 2021, 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 filednormal course of business.
Impact of COVID-19 Pandemic and other geopolitical events
The COVID-19 pandemic has caused many governments to implement measures to slow the spread of the outbreak through quarantines, travel restrictions, heightened border security and other measures. The U.S. Department of Health and Human Services let the public health emergency declaration for COVID-19 expire on May 11, 2023 and the World Health Organization ended the global emergency status for COVID-19 on May 5, 2023. Although the impact has lessened and many of the protective measures associated therewith have been terminated, COVID-19 may continue to affect the global economy as well as businesses and capital markets around the world.

Further, general macroeconomic trends, including rising inflation rates, rising interest rates, as well as recent and potential future disruptions in access to bank deposits or lending commitments due to bank failure, sustained supply chain disruptions, and any resulting recession, depression or other sustained adverse market event could materially and adversely affect our business, financial condition, results of operations and the value of our Common Stock (as defined below).

Additionally, financial markets may be adversely affected by the Company withcurrent or anticipated impact of military conflict, including escalating military fighting between Russia and Ukraine, terrorism, bank failures or other or macroeconomic geopolitical events. The U.S. and other nations in response to the SECRusso-Ukrainian conflict have announced economic sanctions which may have an adverse effect on July 9, 2020the global financial markets. 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 has vendor staff in Ukraine, and with the audited balance sheet includedany political instability in the Form 8-K filed byregion may disrupt resourcing assigned to the Company with the SEC on July 16, 2020.

Emerging Growth Company

trial and negatively impact our business.

The Company is an "emerging growth company,"monitoring the potential impact of the COVID-19 pandemic, the Russo-Ukrainian conflict, bank failures and other macroeconomic 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.
6

Risks and uncertainties
Prior to the Lantheus License Agreements (as defined in Section 2(a) ofNote 3 below), the Securities Act, as modified byCompany had incurred significant net losses and had funded operations primarily through equity financings. Operating losses and negative cash flows were incurred in the Jumpstart our Business Startups Act of 2012 (the "JOBS Act"),quarter ended March 31, 2023 and it may take advantage of certain exemptions from various reporting requirements that are applicableexpected to other publiccontinue to be incurred in future periods. The Company is subject to risks and uncertainties common to early-stage companies that are not emerging growth companiesin the biotechnology industry, including, but not limited to, not being requiredsuccessful discovery and development of its product candidates, regulatory approval of its product candidates, development by competitors of new technological innovations, dependence on key personnel, the ability to complyattract and retain qualified employees, protection of proprietary technology, compliance with governmental regulations, the auditor attestation requirementsimpact of Section 404 of the Sarbanes-Oxley Act, reduced disclosure obligations regarding executive compensation in its periodic reports and proxy statements, and exemptionsmacroeconomic disruptions, such as those arising from the requirementsCOVID-19 coronavirus, the Russo-Ukrainian conflict and adverse developments affecting the financial services industry, the ability to secure additional capital to fund operations and commercial success of holding a nonbinding advisory vote on executive compensationits product candidates. Product candidates currently under development will require extensive preclinical and stockholderclinical testing and regulatory approval prior to commercialization. These efforts require significant amounts of any golden parachute payments not previously approved.

Further, section 102(b)(1) ofcapital, adequate personnel, and infrastructure and extensive compliance-reporting capabilities. Even if the JOBS Act exempts emerging growth companies from being required to comply with new or revised financial accounting standards until private companies (thatCompany’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 to the performance obligations under the Lantheus License Agreements, the accrual of research and development expenses 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,estimates or assumptions.

Recent 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

pronouncements

The Company follows the asset and liability method ofhas evaluated accounting for income taxes under FASB ASC 740, "Income Taxes." Deferred tax assets and liabilities are recognized for the estimated future tax consequences attributable to differences between the financial statements carrying amounts of existing assets and liabilities and their respective tax bases. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. The effect on deferred tax assets 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. 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 anypronouncements 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 reflector disclosures.

3. Revenue
In November 2022, POINT announced strategic collaboration and exclusive license agreements with Lantheus Holdings Inc. ("Lantheus") for exclusive worldwide rights for PNT2002 and PNT2003, excluding certain territories (Japan, South Korea, Singapore, Indonesia, and China including Hong Kong, Macau and Taiwan) (the "PNT2002 Agreement" and "PNT2003 Agreement", respectively, and collectively the stock split.

"Lantheus License Agreements"). The Company filedcollaboration pairs POINT's expertise in next generation radioligand development and manufacturing with Lantheus’ commercial leadership in Prostate-Specific Membrane Antigen ("PSMA") PET and radiopharmaceuticals.


In December 2022, closing conditions for the transaction, including Hart-Scott-Rodino antitrust clearance, were satisfied. POINT received a $250.0 million upfront payment under the PNT2002 Agreement and will receive an Amended 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 Combination and are subject to 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, directors 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, 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 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 for 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 million upfront payment under the PNT2003 Agreement, and will receive up to an additional $30 million upon U.S. regulatory approval. The PNT2003 Agreement also provides that POINT 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,up to $275.0 million.

The Company is responsible for completing the Company had no outstanding Working Capital Loans.

Private Placement of Common Stock

The Sponsor has indicated an interestSPLASH trial and the parties will work together to purchase $25 million offile the Company's common stock in a private placement that would occur concurrentlyNew Drug Application (“NDA”) 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, the Company is not under any obligation to sell any such shares.

Note 5 — 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 into in connection 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.

7

Underwriting


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.
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 million upfront payment and has allocated this to the first two performance obligations based on a 45-day optionrelative standalone selling price basis. The standalone selling prices for the first two performance obligations were determined using adjusted market and expected cost plus a margin assessments, 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 relate 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 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 adjusted market and expected cost plus a margin assessments, 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 relate 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).
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,
8

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 March 31, 2023 and December 31, 2022:
March 31, 2023December 31, 2022
Deferred revenue
Deferred revenue, current$16,518,934 $23,242,290 
Deferred revenue, net of current portion7,444,239 10,178,147 
Total$23,963,173 $33,420,437 
At inception of the Lantheus License Agreements, deferred revenue $34.8 million was recognized in connection with future performance. During the quarter ended March 31, 2023, the Company recognized $9.5 million in revenue for services performed (March 31, 2022 - $nil). 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.
4. Cash, cash equivalents and investments
Cash, cash equivalents and investments consisted of the following:
As of March 31, 2023As of December 31, 2022
Cash$19,393,396 $12,429,627 
Cash equivalents:
Money market funds91,746,221 273,998,744 
Total cash and cash equivalents111,139,617 286,428,371 
Short-term investments
Commercial paper159,747,972 115,156,455 
Corporate bonds67,096,233 45,219,042 
U.S. Government agency debt securities58,250,793 42,577,762 
Asset backed securities33,798,585 35,830,211 
Total short-term investments318,893,583 238,783,470 
Long-term investments
Asset backed securities48,352,696 16,119,430 
Corporate bonds40,817,639 — 
Total long-term investments89,170,335 16,119,430 
Total cash, cash equivalents and investments$519,203,535 $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 March 31, 2023 were as follows:

9

Amortized CostUnrealized GainsUnrealized LossesFair ValueCurrentNon-current
Commercial paper$159,747,972 $— $— $159,747,972 $159,747,972 $— 
Corporate bonds108,167,58515,551$(269,264)107,913,87267,096,23340,817,639 
Asset backed securities82,135,89874,656 (59,273)82,151,28133,798,58548,352,696 
U.S. Government agency debt securities58,268,02027,511(44,738)58,250,79358,250,793— 
Total available-for-sale securities$408,319,475 $117,718 $(373,275)$408,063,918 $318,893,583 $89,170,335 

The following table summarizes the fair value of available-for-sale investments based on stated contractual maturities as of March 31, 2023:
Amortized CostFair Value
Due within one year$319,134,902 $318,893,583 
Due between one and five years89,184,573 89,170,335 
Total$408,319,475 $408,063,918 

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.

During the three months ended March 31, 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 tables present information about the Company’s financial assets and liabilities as of March 31, 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 (in thousands):
10

Level 1Level 2Level 3Total
March 31, 2023
Cash equivalents:
Money market mutual fund$91,746,221 $— $— $91,746,221 
Available-for-sale debt securities:
Commercial paper— 159,747,972 — 159,747,972 
Corporate bonds— 107,913,872 — 107,913,872 
Asset backed securities— 82,151,281 — 82,151,281 
U.S. Government agency debt securities58,250,793 — — 58,250,793 
Total$149,997,014 $349,813,125 $ $499,810,139 

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.

We did not have any financial liabilities measured at fair value on a recurring basis as of March 31, 2023.

There have been no transfers of assets or liabilities between the fair value measurement levels.
6. Prepaid expenses and other current assets
Prepaid expenses and other current assets consisted of the following:
As of March 31, 2023 As of December 31, 2022
$ $
Prepaid clinical trial expenses3,339,239 4,011,419 
Prepaid insurance859,141 1,310,314 
Canadian harmonized sales tax receivable159,045 60,222 
Other189,282 228,934 
Total4,546,707 5,610,889 
7. Property, plant and equipment, net
Property, plant and equipment, net consisted of the following:
As of March 31, 2023 As of December 31, 2022
$ $
Land and building18,451,207 18,163,962 
Machinery and equipment9,015,960 5,328,639 
Property, plant and equipment, in development8,367,969 8,434,384 
Furniture and fixtures721,595 698,728 
Computer equipment149,892 149,892 
36,706,623 32,775,605 
Less: Accumulated depreciation(1,932,656)(1,395,029)
Total34,773,967 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. Property, plant and equipment that have finite lives are recorded at cost less accumulated depreciation and impairment losses. Depreciation is expensed from the datemonth the particular asset
11

is available for its intended use, using the straight-line method over the estimated useful life of such asset at the following rates, which in each case are intended to reduce the carrying value of the final prospectus relatingasset to the Initial Public Offering 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 closingestimated residual value:

Asset CategoryEstimated Useful Life
Computer equipment5 years
Machinery and equipment7 years
Furniture and fixtures7 years
Building20 years
8. Accrued expenses
Accrued liabilities consisted of the Initial Public Offering. An additional fee of $0.35 per share, or approximately $4.8 million in the aggregate, will 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 of its 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 do not include any adjustments that might result from the outcome of this uncertainty.

Note 6 — Stockholder's Equity

Class A common stockfollowing:

As of March 31, 2023As of December 31, 2022
$$
Accrued personnel costs7,660,395 7,116,382 
Accrued research and development costs7,174,563 9,645,594 
Accrued corporate legal fees and other professional services1,536,575 2,068,793 
Accrued costs for purchases of property, plant and equipment41,236 105,741 
Other accrued costs202,297 157,944 
Total16,615,066 19,094,454 
9. 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 March 31, 2023, the Company issued (a) 15,000 shares of Common Stock in connection with such designations, votingthe exercise of stock options granted to a non-employee consultant, resulting in total cash proceeds of $20,850 and other rights(b) 17,936 shares of Common Stock in connection with the exercise of stock options granted to a board member, resulting in total cash proceeds of $125,014.

During the three months ended March 31, 2022, the Company issued 678 shares of Common Stock issued in connection with the exercise of stock options issued to a non-employee consultant, resulting in total cash proceeds of $942.
As of March 31, 2023, the number of total issued and preferencesoutstanding shares of Common Stock was 105,682,677 (December 31, 2022 – 105,649,741). As of March 31, 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. Common stockholders are entitled to receive dividends, if any, as may be determineddeclared by the Company’s board of directors. During the three months ended March 31, 2023, no cash dividends were declared or paid by the Company (March 31, 2022 — $nil).
The Company’s board of directors 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 Delaware General Corporation Law ("DGCL"). During the three months ended March 31, 2023, no shares of Preferred Stock were issued by the Company.
10. Stock-based compensation
In March 2020, the board of 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 Company’s board of directors adopted the POINT Biopharma Global
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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 Company's board of directors. As of June 30, 2020, there was no preferred stock outstanding.

Note 7 — Subsequent Events

January 1, 2023, the number of shares of Common Stock available under the 2021 EIP increased by 4,225,990 for a total of 9,344,912 shares of Common Stock authorized for issuance under the 2021 EIP as of March 31, 2023.

Stock options
The Company evaluated subsequent eventsrecorded $446,128 to research and transactionsdevelopment expense and $563,368 to general and administrative expenses for stock-based compensation for the three months ended March 31, 2023 (March 31, 2022 — $285,311 to research and development expense and $155,139 to general and administrative expenses for the three months ended). The Company did not recognize a tax benefit related to stock-based compensation expense during the three months ended March 31, 2023, 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.
Number of
Shares
Weighted
Average Exercise
Price
$
Weighted-
Average
Remaining
Contractual
Term (in years)
Outstanding as of December 31, 20225,592,1735.85
Granted2,839,8236.78
Exercised(32,936)4.43
Forfeited(33,693)8.25
Expired(9,546)8.47
Outstanding as of March 31, 20238,355,8216.164.8
Vested and expected to vest as of March 31, 20238,355,8216.164.8
Options exercisable as of March 31, 20232,635,8054.614.7
During the three months ended March 31, 2023, 2,839,823 stock options were granted to employees and directors of the Company, with a weighted average grant date fair value of $3.76. The vesting terms of these options are such that occurred after25% of the balance sheet date throughoptions 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 March 31, 2022, 1,705,197 stock options were granted to employees and directors of the Company, with a weighted average grant date fair value of $4.58. The vesting terms of these options are such that 25% of the financial statements were issued. Other than as describedoptions vest on the one-year anniversary of the date of grant and the remaining 75% of such stock options vest in these unaudited condensed financial statementsthree equal annual installments thereafter.

The following table presents the assumptions used in relationthe Black-Scholes-Merton option-pricing model to determine the grant date fair value of stock options granted:
Three months ended March 31, 2023Three months ended March 31, 2022
Risk-free interest rate3.71%1.24% - 2.51%
Expected term (in years)4.254.25
Expected volatility68%72% - 73%
Expected dividend yield
During the three months ended March 31, 2023, non-employee consultants of the Company exercised 15,000 stock options with an intrinsic value of $95,450 and a board member of the Company exercised 17,936 stock options with an intrinsic value of $5,560. The exercises resulted in cash proceeds to the Company's stock split (Note 4), repaymentCompany of $20,850 and $125,014, respectively.
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During the three months ended March 31, 2022, a non-employee consultant of the Note (Note 4)Company exercised 678 stock options with an intrinsic value of $3,210, resulting in the cash proceeds to the Company of $942.
As of March 31, 2023, the unrecognized stock-based compensation expense related to unvested stock options, was $19,961,367 and Initial Public Offering (Note 3) and related transactions,the estimated weighted average remaining vesting period was 2.6 years.
Performance Share Units
During the year ended December 31, 2022, 146,044 performance share units ("PSUs") were granted to employees of the Company, with a grant date fair value of $6.61 per unit based on the closing share price of the Company's Common Stock on the date of grant. The vesting terms of these PSUs are such that 100% vest upon the regulatory approval of PNT2002 by the FDA. During the three months ended March 31, 2023, the Company did not identifyrecord any stock-based compensation expense related to these PSUs on the basis that they still 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.
11. 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 March 31, 2023, the Company is committed to aggregate future payments of approximately $22.4 million in connection with these agreements. During the three months ended March 31, 2023 and March 31, 2022, approximately $2.9 million and $0.6 million, respectively, has been recorded within property, plant and equipment in connection with these agreements.
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 product 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 $3.6 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 its supply agreements of approximately $6.5 million during the three months ended March 31, 2023 (three months ended March 31, 2022 – $1.7 million).
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 $109.5 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 in connection with these agreements during the three months ended March 31, 2023 (three months ended March 31, 2022 - $nil).
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 10 year contract term.
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 $23.4 million with payments that range from one to five years. The Company recorded research and development expenses in connection with this agreement of approximately $4.9 million during the three months ended March 31, 2023 (three months ended March 31, 2022 – $3.1 million).
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 in the 2022 Financial Statements.
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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. In consideration, the Company will make a payment of 2.15 million as well as minimum annual licenses fees ranging from 10-50 thousand. The Company is also obligated to make an additional milestone payment to Scintomics of €5 million upon the achievement of a specified regulatory milestone. See Note 15.
The Company recorded research and development expenses in connection to its license agreements of approximately $0.5 million during the three months ended March 31, 2023 (three months ended March 31, 2022 – $0.8 million).
12. 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
 March 31, 2023
Three months
ended
March 31, 2022
Net loss attributable to common stockholders$16,530,671 $16,380,574 
Weighted-average common shares outstanding-basic and diluted105,660,655 90,122,269 
Net loss per share attributable to common stockholders-basic and diluted$0.16 $0.18 
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 performance share units are considered contingently issuable shares for the purpose of the computation of loss per share and have been excluded on the basis that as at March 31, 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 common stockholders is the same.
13. Income Taxes
The Company calculates its interim tax provision, at the end of each interim period, the Company estimates the annual effective tax rate and applies that 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, as such it is subject to tax in both countries. The income tax expense for the three months ended March 31, 2023 and March 31, 2022 was $(238,642) and $88,116 respectively. The income tax benefit for the three months ended March 31, 2023, consists primarily of tax benefit for research and development tax credits partially offset by current taxes in Canada. The income tax benefit for the three months ended March 31, 2022, consists of current taxes in Canada.
The Company files income tax returns in the U.S. federal, certain state, 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 March 31, 2023, the Company believes no significant changes in the unrecognized tax benefits will occur within the next 12 months.


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14. Related party transactions
The Company recognized expenses in connection with related party transactions in the unaudited interim condensed consolidated statements of operations as follows:
Three months ended
March 31, 2023
Three months ended
March 31, 2022
Consulting fees on business activities to Board member$174,415 $66,696 
Reimbursement to Board member for occupancy costs17,419 17,778 
Total$191,834 $84,474 
Transactions with related parties are in the normal course of operations and have been measured at their agreed upon exchange amount.
During the three-month periods ended March 31, 2023 and 2022, the Company received consulting services for research and development from a Board member. As of March 31, 2023, $107,650 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 Topic 842, Leases to this arrangement and is recording the lease payments of approximately $6,000 monthly as rent expense.
15. Subsequent events
License Agreement Amendments

On April 17, 2023, POINT Biopharma Inc. entered into the Amendments to that certain sublicense agreement, dated November 14, 2019, between POINT Biopharma Inc. and 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. In consideration, the Company will make a payment of 2.15 million as well as minimum annual licenses fees ranging from 10-50 thousand. The Company is also obligated to make an additional milestone payment to Scintomics of €5 million upon the achievement of a specified regulatory milestone.
Convertible Note

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. Pursuant to the Convertible Note Agreement, upon execution and subject to certain closing conditions, the Company will purchase $10 million in unsecured promissory notes convertible into common stock of Ionetix-α at a conversion price that is subject to certain conditions as defined in the Convertible Note Agreement.

Supply Agreement

On May 10, 2023, the Company entered into the Irradiation Agreement, pursuant to which the Company will receive irradiation services to irradiate 176Yb. See Note 11.
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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 months ended March 31, 2023 (the “Q1 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 and the volatility of the market price of our common stock, par value $0.0001 per share ("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, 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 supply chain is often overlooked, the Company has carved out a unique advantage for itself: a 100% Company-owned facility, located in Indianapolis, Indiana, which includes an office space occupying 10,500 square feet and a manufacturing facility occupying 70,200 square feet, and which we believe has the capacity for expansion to commercially supply both North America and Europe with large volumes. Furthermore, management has leveraged their prior relationships to assemble resilient radioisotope supply chains for the Company, which even includes manufacturing the Company's 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

Subsequent to the quarter, we announced the U.S. Food and Drug Administration (FDA) granted Fast Track designation for 177Lu-PNT2002 for the purposetreatment of effectingmetastatic castration resistant prostate cancer (mCRPC). Fast track is a merger,process designed to facilitate the development and expedite the review of drugs to treat serious conditions and address unmet medical needs. Enrollment in PNT2002's SPLASH trial (NCT04647526) is complete and top line data is expected in the second half of 2023.

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

We initiated our phase 1 FRONTIER clinical trial for PNT6555 in July 2022 in Canada using a 68Ga-based PNT6555 molecular imaging agent to select patients to receive a n.c.a. 177Lu-based PNT6555 therapeutic agent. FRONTIER's clinical protocol evaluates PNT6555 in approximately 30 patients in five FAP-avid cancer indications: colorectal, pancreatic, esophageal, melanoma, and soft tissue sarcoma. Enrollment in cohort 3 of the phase 1 FRONTIER trial (NCT05432193) began in the second quarter of 2023, and a total of seven participants have been dosed with 177Lu-PNT6555 to date. We anticipate data from the full FRONTIER study to be available in the first half of 2024.

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

PNT2001 builds on POINT’s first-generation, lutetium-based program with a next-generation ligand optimized for use with the alpha-emitting radioisotope actinium-225. The lead of the PNT2001 program is 225Ac-PSMA-62. We now anticipate a
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health authority submission for 225Ac-PSMA-62 in Q4 2023, with the first patient expected for a phase 1 clinical trial in Q1 2024.

To ensure consistent and reliable supply ahead of our first 225Ac in-human trial, we expanded our partnership with Ionetix and recently added another supplier in Eckert & Ziegler. We have established redundant 225Ac supply with partners who have access to rare thorium and radium sources, and who are pursuing a variety of production methods. Our partners include the U.S. Department of Energy Isotope Program (managed by the Office of Isotope R&D and Production), as well as agreements for future access from Ionetix, TerraPower, NorthStar Medical Radioisotopes, and Eckert & Ziegler.

Manufacturing & Supply Chain Updates

In February 2023, we entered into a Facility Agreement with University Health Network (“UHN”) that authorizes us to access and utilize a 7,700 square foot, licensed research and development space with cGMP manufacturing suites. The facility is fully operational, licensed for alpha, beta, gamma, and positron emitters, has a PETtraceTM 800 cyclotron and hot cells, and is located in Toronto, Canada, in a translational institute & research hospital network. The facility, now referred to as the POINT Institute for Radioligand Innovation ("PIRI"), will be used to develop and expand our pipeline of next-generation radiopharmaceuticals.

In April 2023, we announced an agreement for the supply of actinium-225 (225Ac) with Eckert & Ziegler. Eckert & Ziegler will provide predetermined amounts of GMP grade 225Ac to POINT for use in the development of POINT’s pipeline of next generation 225Ac-based radioligands. In addition to our manufacturing facility in Indianapolis, Indiana, we also maintain active relationships with radiopharmaceutical contract manufacturers and isotope suppliers across multiple geographies.

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 225Ac. IONETIX has transferred its alpha therapy isotope business assets into Ionetix-α. POINT will invest $10 million into Ionetix-α.

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 months ended March 31, 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. However, this does not reflect the possibility that we may not be able to access a portion of our initial Business Combination. We cannot assure you that our plansexisting cash, cash equivalents and investments due to raise capitalmarket conditions. If additional banks and financial institutions enter receivership or to complete our initial Business Combination will be successful.

Results of Operations and Known Trends or Future Events

We have neither engaged 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 completion of our initial Business Combination. We will generate non-operating incomebecome insolvent in the formfuture in response to financial conditions affecting the banking system and financial markets, our ability to access our

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cash and cash equivalents after our Initial Public Offering. There has been no significant change in our financial or trading position and noinvestments may be threatened and could have a material adverse change has occurred sinceeffect on our business and financial condition.
We are subject to risks and uncertainties common to early-stage companies in the datebiotechnology industry, including, but not limited to, successful discovery and development of our auditedproduct 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 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 anticipate that our expenses 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 identify, 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 statements. Afterand management systems and increase personnel to support our Initial Public Offering,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 expectmay receive regulatory approval in regions where we choose to incur increased expensescommercialize our products on our own or jointly with third parties.
COVID-19 Pandemic and other geopolitical events
The COVID-19 pandemic has caused many governments to implement measures to slow the spread of the outbreak through quarantines, travel restrictions, heightened border security and other measures. The U.S. Department of Health and Human Services let the public health emergency declaration of COVID-19 expire on May 11, 2023 and the World Health Organization ended the global emergency status for COVID-19 on May 5, 2023. Although the impact has lessened and many of the protective measures associated therewith have been terminated, COVID-19 may continue to affect the global economy as well as businesses and capital markets around the world.
Further, general macroeconomic trends, including rising inflation rates, rising interest rates, as well as recent and potential future disruptions in access to bank deposits or lending commitments due to bank failure, sustained supply chain disruptions, and any resulting recession, depression or other sustained adverse market event could materially and adversely affect our business, financial condition, results of operations and the value of our Common Stock.

Additionally, financial markets may be adversely affected by the current or anticipated impact of military conflict, including escalating military fighting between Russia and Ukraine, terrorism or other geopolitical events. The U.S. and other nations in response to the Russo-Ukrainian conflict have announced economic sanctions which may have an adverse effect on the global financial markets, which, in turn, could have an adverse effect on our business, financial condition and results of operations. The Company's SPLASH trial has vendor staff in Ukraine, and any political instability in the region may disrupt resourcing assigned to the trial and negatively impact our business.

We are monitoring the potential impact of the COVID-19 pandemic, the impact of the Russo-Ukrainian conflict and adverse developments affecting the financial services industry on our business and financial results. To date, we have not experienced any material business disruptions or incurred any impairment losses in the carrying values of our assets 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 Q1 2023 Financial Statements.
Components of Operating Results
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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 public company (for legal, financial reporting, accounting,discussion of the nature of our operating expense line items within our accompanying condensed consolidated statements of operations.
Results of Operations
The following table summarizes our results of operations for the three months ended March 31, 2023 and auditing compliance),2022:
For the three
months ended
March 31, 2023
For the three
months ended
March 31, 2022
Change
(In U.S. dollars)$$$%
Revenue
Other revenue9,457,264 — 9,457,264 100.0 %
Total revenue9,457,264 — 9,457,264 100.0 %
Operating expenses:    
Research and development26,910,472 12,500,848 14,409,624 115.3 %
General and administrative5,010,129 3,807,942 1,202,187 31.6 %
Total operating expenses31,920,601 16,308,790 15,611,811 95.7 %
Loss from operations(22,463,337)(16,308,790)(6,154,547)37.7 %
Other income (expenses):
Investment income5,764,214 47,973 5,716,241 11,915.5 %
Foreign currency loss(70,190)(31,641)(38,549)121.8 %
Total other income (expenses)5,694,024 16,332 5,677,692 34,764.2 %
Loss before income taxes(16,769,313)(16,292,458)(476,855)2.9 %
Income tax benefit (provision)238,642 (88,116)326,758 370.8 %
Net loss(16,530,671)(16,380,574)(150,097)0.9 %
Research and Development
The following table summarizes the components of research and development expense for the three months ended March 31, 2023 and 2022:
For the three
months ended
March 31, 2023
For the three
months ended
March 31, 2022
Change
(In U.S. dollars)$$$%
Clinical trials8,888,420 4,729,141 4,159,279 87.9 %
Salaries and benefits6,643,811 3,738,530 2,905,281 77.7 %
Contract manufacturing8,232,349 2,709,583 5,522,766 203.8 %
Depreciation and overhead2,349,513 508,221 1,841,292 362.3 %
Sponsored research & product licenses500,000 750,000 (250,000)(33.3)%
Regulatory consulting296,379 65,373 231,006 353.4 %
Total26,910,472 12,500,848 14,409,624 115.3 %

For the three months ended March 31, 2023 as wellcompared to the three months ended March 31, 2022, the increase in research and development expense 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 the completion ofexpand its research and development headcount, most notably in our Initial Public Offering through receipt of a $25,000 capital contribution from our Sponsor in exchange for the issuance of the Founder SharesIndianapolis manufacturing facility and (c) depreciation and overhead related to our Sponsormanufacturing 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 March 31, 2023, the Company incurred approximately $11.6 million and $1.2 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.

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General and administrative
General and administrative expenses increased for the sharesthree months ended March 31, 2023 as compared to the three months ended March 31, 2022, primarily in connection with increased headcount compared to the prior year period.
Other Income (Expenses)
For the three months ended March 31, 2023 and 2022, other income (expenses) consist mainly of Class A common stock in our Initial Public Offering, after deducting offering expenses 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 interestincrease in investments primarily in connection with cash received in connection with equity financings and the Lantheus License Agreements.

Income Tax Expense
For the three months ended March 31, 2023, income earned ontax 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 amountCanadian subsidiary of the Company. For the three months ended March 31, 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
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 in the Trust Account (if any)three months ended March 31, 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, including, but not limited to, successful discovery and development of our 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 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 $16.5 million and $16.4 million for the three months ended March 31, 2023 and 2022, respectively.
On September 16, 2022, we issued 13,900,000 shares of Common Stock in connection with the 2022 Public Offering 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 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 and licensing of additional product candidates, and to support 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.
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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, 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 March 31, 2023, we had cash, cash equivalents and investments of approximately $519.2 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 pursuant to a distribution agreement with Piper Sandler & Co. No shares of Common Stock were issued in connection with the ATM as of December 31, 2022. Pursuant to the Form S-3, on September 16, 2022 we issued 13,900,000 shares of Common Stock in connection with a public offering 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

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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 because we do not have sufficient funds availableresearch, product development or future commercialization efforts, or grant rights to us, we will be forced to cease operationsdevelop and liquidate the Trust Account.


Related Party Transactions

Founder Shares

On April 30, 2020, our 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"). In June 2020, our Sponsor transferred 30,000 founder shares to each of Messrs. Grau, Gray and Lubner.

We filed an Amended and Restated Certificate of Incorporation on June 15, 2020, suchmarket product candidates that we are authorizedwould otherwise prefer to issue sharesdevelop and market ourselves.


Going Concern
We assess and determine our ability to continue as a going concern in accordance with the provisions of Class B common stock. PursuantASC Topic 205-40, Presentation of Financial Statements—Going Concern. We have determined 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 March 31, 2023 and December 31, 2022:
As of
March 31,
2023
As of
December 31,
2022
Change
(In U.S. dollars)$$$%
Current assets434,579,907 530,822,730 (96,242,823)(18.1)%
Current liabilities77,847,838 79,738,440 (1,890,602)(2.4)%
Total working capital356,732,069 451,084,290 (94,352,221)(20.9)%
The decrease in working capital as of March 31, 2023, primarily reflects cash used a) to the amendment, the Founder Shares were converted into shares of Class B common stock. On July 8, 2020,purchase long-term investments, b) for operating expenses, including, personnel costs and research and development costs as we effected a 1:1.18 stock split ofadvance our Class B common stock, resultingclinical trials and continue to expand our pipeline, and (c) for capital expenditures for equipment and machinery used in our sponsor holding an aggregatemanufacturing facility in Indiana.
Cash Flows
The following table summarizes our sources and uses of 3,286,300 founder sharescash for the three months ended March 31, 2023 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 at2022:

For the three
months ended
March 31, 2023
For the three
months ended
March 31, 2022
Change
(In U.S. dollars)$$$%
Net cash flows used in operating activities(22,391,341)(10,490,604)(11,900,737)113.4 %
Net cash flows used in investing activities(153,043,277)(940,931)(152,102,346)16,165.1 %
Net cash flows provided by financing activities145,864 942 144,922 15384.5 %
Net decrease in cash and cash equivalents(175,288,754)(11,430,593)(163,858,161)1433.5 %
Cash flows used in operating activities
Net cash flows used in operating activities represent the time of our initial Business Combinationcash receipts and are subjectdisbursements related 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 rightthree months ended March 31, 2023 compared to exchange their common stock for cash, securities or other property.

Private Placement Shares

Concurrently with the closingthree months ended March 31, 2022 as we advance our clinical trials and continue to expand our pipeline, as described above.

24

We believe that the Initialnet proceeds from the Lantheus License Agreements and the 2022 Public Offering, together with our Sponsor purchased 471,400 Private Placement Shares, at a priceavailable resources and existing cash and cash equivalents, are sufficient to fund our operating expenses and capital expenditure requirements into 2026.

Cash flows used in Investing Activities
For the three months ended March 31, 2023 and 2022, net cash used in investing activities totaled $153.0 million and $0.9 million, respectively. The increase in cash used in investing activities relates to (a) the Company's investment of $10.00 per share in a private placementits available cash resources into fixed income investments and (b) increased capital expenditures for 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 of our unaudited condensed financial statements.

The Sponsor and our 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 us an aggregate of up to $300,000 to cover expenses related to the Initial Public Offering pursuant to a promissory note (the "Note"). In May 2020, we 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 costspurchases in connection with a Business Combination,our Indianapolis manufacturing facility.

Cash flows provided by Financing Activities
For the Sponsor or an affiliatethree months ended March 31, 2023 and 2022, net cash provided by financing activities totaled $0.1 million and $1 thousand, respectively, which consisted of the Sponsor, or certainnet proceeds received from the exercise of our officersstock options.
Contractual Obligations 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 heldOther Commitments
The Company in the Trust Account would be used to repay the Working Capital Loans. Except for the foregoing, the termsnormal course of such Working Capital Loans, if any, have not been determinedbusiness enters into various services and no writtensupply 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 into in connection with its clinical trials to ensure the consummationsupply of certain product and product lines during the Initial Public Offering. Holders of 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 11 to the Initial Public OfferingQ1 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 11 to the underwriters for deferred underwriting commissions. The deferred underwriting commissions will become payableQ1 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 as definedor 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 Q1 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 Q1 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 at the date of the Q1 2023 Financial Statements and the reported amounts of expenses during the reporting 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

The JOBS Act contains provisions that, among other things, relax certain reporting requirements for qualifying public companies. We qualify as an "emerging growth company"Financial Condition and underResults of Operations,” in our 2022 Form 10-K.

ITEM 3. – QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
Market risks relating to our operations result primarily from interest rate risk and foreign exchange risk. As of March 31, 2023, there were no material changes to our market risks from the JOBS Act will be allowed to comply with new or revised accounting pronouncements based on the effective date for private (not publicly traded) companies. We are electing to delay the adoption of new or revised accounting standards, and as a result, we may not comply with new or revised accounting standards on the relevant dates on which adoption of such standards is required for non-emerging growth companies. As 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, we areinformation provided in the process of evaluating the benefits of relying on the other reduced reporting requirements provided by the JOBS Act. Subject to certain conditions set forth in the JOBS Act, if, as an "emerging growth company," we choose to rely on such exemptions we may not 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 of the compensation disclosure that may be required of non-emerging growth public companies under the Dodd-Frank Wall Street Reform 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 such as the correlation between executive compensation and performance and comparisons of the CEO's compensation 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.Quantitative7A “Quantitative and Qualitative Disclosures aboutAbout Market Risk.

AsRisk” in our 2022 Form 10-K.


25

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 months ended March 31, 2023 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.

Item2022.





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 March 31, 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 March 31, 2023, our disclosure controls and procedures were effective.
Changes in Internal Control over Financial Reporting

There

During the fiscal quarter ended March 31, 2023 we continued to (i) adopt, improve and maintain policies, processes and documentation procedures to improve the overall efficiency and accuracy of our financial reporting; and (ii) work with third-party consultants to review the design of our systems of internal control over financial reporting and recommend improvements. As part of this process, during the fiscal quarter ended March 31, 2023, we continued to refine our processes in respect of our new general ledger system to improve our internal control framework.
Except as disclosed above, 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-QMarch 31, 2023 that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.

21

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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 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 March 31, 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 Offeringquarter ended March 31, 2023.
ITEM 3. – DEFAULTS UPON SENIOR SECURITIES.
None.
ITEM 4. – MINE SAFETY DISCLOSURES.
Not applicable.
ITEM 5. – OTHER INFORMATION.
None.
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ITEM 6. – EXHIBITS.
The following exhibits are filed as part of Class A common stock, 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 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
Investment Management Trust Agreement, dated July 7, 2020, by and between the Company and Continental Stock Transfer & Trust Company, as trustee (IncorporatedBy-laws of POINT Biopharma Global Inc. (incorporated by reference to Exhibit 10.13.2 to the Registrant’s Current Report on Form 8-K filed by the Company on July 10, 2020)1, 2021).
10.1*#
10.231.1*Registration and Stockholder Rights Agreement, dated July 7, 2020, by and among the Company, Therapeutics Acquisition Holdings, LLC and the other holders party thereto(Incorporated by reference to Exhibit 10.2 to the Registrant’s Current Report on Form 8-K filed on July 10, 2020).
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.
28

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: May 15, 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)


29