Exhibit 99.2
NEOLEUKIN THERAPEUTICS, INC.
Financial Statements
June 30, 2019
NEOLEUKIN THERAPEUTICS, INC.
INDEX TO FINANCIAL STATEMENTS
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2
Neoleukin Therapeutics, Inc.
June 30, 2019 (Unaudited) | December 31, 2018 (Audited) | |||||||
Assets | ||||||||
Current assets: | ||||||||
Cash | $ | 4,109,595 | $ | 3,456,427 | ||||
Prepaid expenses and other current assets | 634,443 | 52,735 | ||||||
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Total current assets | 4,744,038 | 3,509,162 | ||||||
Property and equipment, net | 856,559 | 7,093 | ||||||
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Total assets | $ | 5,600,597 | $ | 3,516,255 | ||||
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Liabilities and stockholders’ deficiency | ||||||||
Current liabilities: | ||||||||
Finance lease liability | $ | 55,674 | — | |||||
Accounts payable with related parties | 1,975 | 46,538 | ||||||
Accounts payable and other current liabilities | 824,212 | — | ||||||
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Total current liabilities | 881,861 | 46,538 | ||||||
Convertible promissory notes | 7,000,000 | 3,500,000 | ||||||
Finance lease liability, net of current portion | 145,813 | — | ||||||
Other liabilities | 138,110 | 11,731 | ||||||
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Total liabilities | 8,165,784 | 3,558,269 | ||||||
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Commitments and contingency (note 7) | ||||||||
Stockholders’ deficiency: | ||||||||
Common stock; $0.00001 par value: 20,000,000 shares authorized; 9,500,000 shares issued; 5,279,618 and 4,711,130 shares outstanding at June 30, 2019 and December 31, 2018, respectively | 53 | 47 | ||||||
Additionalpaid-in capital | 5,227 | 4,664 | ||||||
Accumulated deficit | (2,570,467 | ) | (46,725) | |||||
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Total stockholders’ deficiency | (2,565,187 | ) | (42,014) | |||||
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Total liabilities and stockholders’ deficiency | $ | 5,600,597 | $ | 3,516,255 | ||||
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See accompanying notes to unaudited interim financial statements.
3
Neoleukin Therapeutics, Inc.
(Unaudited)
Six Months Ended June 30, 2019 | Period from June 4, 2018 (inception) through June 30, 2018 | |||||||
Operating expenses: | ||||||||
Research and development | $ | 1,074,420 | $ | — | ||||
General and administrative | 1,351,018 | 1,123 | ||||||
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Loss from operations | (2,425,438 | ) | (1,123 | ) | ||||
Interest expense | (126,948 | ) | — | |||||
Interest income | 28,644 | — | ||||||
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Net loss | $ | (2,523,742 | ) | $ | (1,123 | ) | ||
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See accompanying notes to unaudited interim financial statements.
4
Neoleukin Therapeutics, Inc.
Statements of Changes in Stockholders’ Deficiency
(Unaudited)
Common stock | Additional paid-in capital | Accumulated deficit | Total | |||||||||||||||||
Shares | Amount | |||||||||||||||||||
Balance at January 1, 2019 | 4,711,130 | $ | 47 | $ | 4,664 | $ | (46,725) | $ | (42,014) | |||||||||||
Vesting of shares previously subject to repurchase | 568,488 | 6 | 563 | — | 569 | |||||||||||||||
Net loss | — | — | — | (2,523,742) | (2,523,742) | |||||||||||||||
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Balance at June 30, 2018 | 5,279,618 | $ | 53 | $ | 5,227 | $ | (2,570,467 | $ | (2,565,187) | |||||||||||
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Common stock | Additional paid-in capital | Accumulated deficit | Total | |||||||||||||||||
Shares | Amount | |||||||||||||||||||
Balance at June 4, 2018 (inception) | — | $ | — | $ | — | $ | — | $ | — | |||||||||||
Net loss | — | — | — | (1,123) | (1,123) | |||||||||||||||
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Balance at June 30, 2018 | — | $ | — | $ | — | $ | (1,123) | $ | (1,123) | |||||||||||
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See accompanying notes to unaudited interim financial statements.
5
Neoleukin Therapeutics, Inc.
(Unaudited)
Six Months Ended June 30, 2019 | Period from June 4, 2018 (inception) through June 30, 2018 | |||||||
Cash flows from operating activities: | ||||||||
Net loss | $ | (2,523,742) | $ | (1,123) | ||||
Adjustments to reconcile net loss to net cash used in operating activities: | ||||||||
Depreciation | 12,542 | — | ||||||
Non-cash interest expense | 126,948 | — | ||||||
Change in operating assets and liabilities: | ||||||||
Prepaid expenses and other assets | (581,708) | — | ||||||
Accounts payable with related parties | (44,563) | 1,123 | ||||||
Accounts payable and other current liabilities | 824,212 | — | ||||||
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Net cash used in operating activities | (2,186,311) | — | ||||||
Cash flows from investing activities: | ||||||||
Purchases of property and equipment | (600,889) | — | ||||||
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Net cash used in investing activities | (600,889) | — | ||||||
Cash flows from financing activities: | ||||||||
Payment of finance lease liability | (59,632) | — | ||||||
Proceeds from convertible promissory notes | 3,500,000 | — | ||||||
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Net cash provided by financing activities | 3,440,368 | — | ||||||
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Net increase in cash | 653,168 | — | ||||||
Cash at the beginning of period | 3,456,427 | — | ||||||
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Cash at the end of period | $ | 4,109,595 | $ | — | ||||
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Supplemental disclosure ofnon-cash financing activities: | ||||||||
Vesting of shares previously subject to repurchase | $ | 569 | $ | — | ||||
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Disposal of property and equipment in exchange for leased equipment | $ | 26,294 | $ | — | ||||
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Finance lease liability in connection with purchase of property and equipment | $ | 287,413 | $ | — | ||||
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See accompanying notes to unaudited interim financial statements.
6
Notes to Unaudited Interim Financial Statements
(1) | Organization and Description of Business |
Neoleukin Therapeutics, Inc. (the “Company”) is a biotechnology company that creates next generation immunotherapies using breakthrough de novo protein design technology. The Company was incorporated on June 4, 2018 in the state of Delaware and has not yet generated any revenue from the sale of products. Through June 30, 2019, its efforts have been principally devoted to debt and equity financings and licensing and collaboration arrangements.
In August 2019, the Company entered into a merger transaction with Aquinox Pharmaceuticals, Inc, (“Aquinox”). Upon completion of the merger, Aquinox was renamed Neoleukin Therapeutics, Inc. and is trading under the new ticker symbol “NLTX” on the Nasdaq Global Market (see Note 10).
(2) | Risks and Liquidity |
The Company has incurred losses and negative cash flows from operations since June 4, 2018 (inception) and has an accumulated deficit of $2,570,467 as of June 30, 2019. The Company anticipates incurring additional losses until such time, if ever, that it can generate significant sales of its product candidate currently in development. Substantial financing will be needed by the Company to fund its operations and to commercially develop its product candidate.
The Company’s operations have consisted primarily of organizing the Company. The Company faces risks associated with companies whose products are in development. These risks include the need for additional financing to complete its research and development, achieving its research and development objectives, defending its intellectual property rights, recruiting and retaining skilled personnel, and dependence on key members of management.
(3) | Summary of Significant Accounting Policies |
Basis of Presentation
The accompanying unaudited interim financial statements have been prepared in accordance with accounting principles generally accepted in the United States of America (GAAP). Any reference in these notes to applicable guidance is meant to refer to GAAP as found in the Accounting Standards Codification (ASC) and Accounting Standards Updates (ASU) promulgated by the Financial Accounting Standards Board (FASB).
In the opinion of management, the accompanying unaudited interim financial statements of the Company include all normal and recurring adjustments (which consist primarily of accruals, estimates and assumptions that impact the unaudited interim financial statements) considered necessary to present fairly the Company’s financial position as of June 30, 2019, its results of operations and cash flows for the six months ended June 30, 2019 and for the period from June 4, 2018 (inception) through June 30, 2018. Operating results for the six months ended June 30, 2019 are not necessarily indicative of the results that may be expected for the year ending December 31, 2019.
The unaudited interim financial statements presented herein do not contain all of the required disclosures under GAAP for annual financial statements. The accompanying unaudited interim financial statements should be read in conjunction with the annual audited financial statements and related notes as of and for the period from June 4, 2018 (inception) through December 31,
7
Neoleukin Therapeutics, Inc.
Notes to Unaudited Interim Financial Statements
2018 filed as an exhibit 99.1 within Form8-K/A on October 10, 2019. Accordingly, they do not include all of the information and footnotes required by GAAP for complete financial statements.
Use of Estimates
The preparation of unaudited interim financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenue and expenses during the reporting period. Actual results could differ from those estimates.
Estimates and assumptions are periodically reviewed and the effects of the revisions are reflected in the accompanying unaudited interim financial statements in the period they are determined to be necessary. Significant areas that require management’s estimates include the fair value of common stock, stock-based compensation assumptions and the accruals forpre-clinical development and clinical trials.
Fair Value of Financial Instruments
Management believes that the carrying amounts of the Company’s financial instruments, including cash and accounts payable, approximate fair value due to the short-term nature of those instruments. Due to the related-party relationship of the convertible promissory noteholders, it is impractical to determine the fair value of the convertible promissory notes.
Concentration of Risk
Financial instruments that potentially subject the Company to concentrations of credit risk consist primarily of cash. The Company places its cash withhigh-credit-quality financial institutions and invests in a money market fund and government agency obligations. The Company has established guidelines relative to credit ratings and maturities that seek to maintain safety and liquidity.
Research and Development
Research and development costs are charged to expense as incurred and consist primarily of salaries, benefits, and other related costs for personnel serving in the research and development functions as well as payments to third-party service providers and related supply and manufacturing costs. At the end of the reporting period, the Company compares payments made to third-party service providers to the estimated progress toward completion of the research or development objectives. Such estimates are subject to change as additional information becomes available. Depending on the timing of payments to the service providers and the progress that the Company estimates has been made as a result of the service provided, the Company may record net prepaid or accrued expense relating to these costs. Costs incurred in obtaining patent and other intellectual property licenses for which there are no alternative future uses are charged to expense as incurred.
8
Neoleukin Therapeutics, Inc.
Notes to Unaudited Interim Financial Statements
Income Taxes
Income taxes are accounted for under theasset-and-liability method as required by FASB ASC Topic 740,Income Taxes,(ASC 740). Deferred tax assets and liabilities are recognized for the future tax consequences attributable to differences between the financial statement carrying amounts of existing assets and liabilities and their respective tax bases and operating loss and tax credit carryforwards. 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 corresponding to the enactment date. Under ASC 740, a valuation allowance is required when it is more likely than not all or some portion of the deferred tax assets will not be realized through generating sufficient future taxable income.
FASB ASC Subtopic 740-10,Accounting for Uncertainty of Income Taxes,(ASC 740-10), defines the criterion an individual tax position must meet for any part of the benefit of the tax position to be recognized in financial statements prepared in conformity with GAAP. The Company may recognize the tax benefit from an uncertain tax position only if it is more likely than not such tax position will be sustained on examination by the taxing authorities, based solely on the technical merits of the respective tax position. The Company does not have unrecognized tax benefits as of December 31, 2018 or June 30, 2019. The Company recognizes interest and penalties accrued on any unrecognized tax benefits as a component of income tax expense.
Fair Value of Financial Instruments
Fair value is the price that could be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants. Fair value determination in accordance with applicable accounting guidance requires that a number of significant judgments are made. Additionally, fair value is used on a nonrecurring basis to evaluate assets for impairment or as required for disclosure purposes by applicable accounting guidance on disclosures about fair value of financial instruments. Depending on the nature of the assets and liabilities, various valuation techniques and assumptions are used when estimating fair value. The carrying amounts of certain of the Company’s financial instruments, including cash, accounts receivable, prepaid expenses and other current assets, other assets and accounts payable are shown at cost, which approximates fair value due to the short-term nature of these instruments. The Company follows the provisions of FASB ASC Topic 820,Fair Value Measurement, for financial assets and liabilities measured on a recurring basis. The guidance requires fair value measurements be classified and disclosed in one of the following three categories:
• | Level 1: Unadjusted quoted prices in active markets that are accessible at the measurement date for identical, unrestricted assets or liabilities |
• | Level 2: Quoted prices in markets that are not active, or inputs which are observable, either directly or indirectly, for substantially the full term of the asset or liabilities |
• | Level 3: Prices or valuation techniques that require inputs that are both significant to the fair value measurement and unobservable (i.e., supported by little or no market activity) |
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Neoleukin Therapeutics, Inc.
Notes to Unaudited Interim Financial Statements
There were no assets or liabilities that required the measurement at fair value on a recurring basis as of June 30, 2019 and December 31, 2018.
Recently Issued Accounting Pronouncements
In March 2016, the FASB issuedASU No. 2016-09,Compensation—Stock Compensation (Topic 718): Improvements to Employee Share-Based Payment Accounting, which simplifies certain aspects of the accounting forshare-based payment transactions, including impact on income taxes, classification of awards, and classification in the statement of cash flows. The Company adopted this standard in 2018 and it did not have a material impact on the Company’s financial statements.
In June 2018, the FASB issued ASU2018-07,Compensation—Stock Compensation (Topic 718) Improvements to Nonemployee Share-Based Payment Accounting. The amendments in this update expand the scope of Topic 718 to include share-based payment transactions for acquiring goods and services from nonemployees. Under this ASU, an entity should apply the requirements of Topic 718 to nonemployee awards except for specific guidance on inputs to an option pricing model and the attribution of costs (that is, the period of time over which share-based payment awards vest and the pattern of cost recognition over that period). The guidance is applicable to public business entities for fiscal years beginning after December 15, 2019, and interim periods within those years, with early adoption permitted. The Company is currently evaluating the effect that this guidance will have on its financial statements and related disclosures.
In August 2018, the FASB issued ASU2018-03,Disclosure Framework—Changes to the Disclosure Requirements for Fair Value Measurements,which changes the fair value measurement disclosure requirements of ASC 820. The goal of the ASU is to improve the effectiveness of ASC 820’s disclosure requirements. The standard is applicable to public business entities for fiscal years beginning after December 15, 2019, and interim periods within those years. The Company is currently evaluating the potential impact of the adoption of this standard on its financial statements and related disclosures.
In February 2016, the FASB issued ASU No. 2016 02,Leases, which requires a lessee to record a right of use asset and a corresponding lease liability on the balance sheet for all leases with terms longer than 12 months. A modified retrospective transition approach is required, applying the new standard to all leases existing at the date of initial application. An entity may choose to use either (1) its effective date, or (2) the beginning of the earliest comparative period presented in the financial statements as its date of initial application. If an entity chooses the second option, the transition requirements for existing leases also apply to leases entered into between the date of initial application and the effective date. The standard is effective for the Company beginning January 1, 2019, with early adoption permitted. The Company adopted this standard on January 1, 2019 and it did not have a material impact on the Company’s financial statements (Note 5).
(4) | Property Plant and Equipment |
Property and equipment are primarily comprised of laboratory equipment and are recorded at cost and depreciated using the straight-line method over their estimated useful lives of five to seven years. Expenditures for routine maintenance and repairs are charged to expense as incurred and costs of improvements and renewals are capitalized. As of June 30, 2019, and December 31, 2018, the gross cost of laboratory equipment was $867,786 and $7,093 and accumulated depreciation was $11,227 and zero, respectively.
10
Neoleukin Therapeutics, Inc.
Notes to Unaudited Interim Financial Statements
At June 30, 2019, $287,413 represents laboratory equipment in connection with the financing lease liability (Note 5). The laboratory equipment is being amortized on a straight-line basis over a useful life of seven years. As of June 30, 2019, the net carrying amount of the laboratory equipment was $287,413.
Depreciation expense for the six months ended June 30, 2019 was $12,542, of which zero was attributable to the amortization of laboratory equipment subject to the financing lease liability.
(5) | Finance Lease |
The Company determines if an arrangement is or contains a lease at inception. Leases with an initial term of less than 12 months are not recorded in the Company’s unaudited interim balance sheets. In May 2019, the Company entered into an equipment lease whereby all rights and title will transfer to the Company upon receipt of the final payment. The discount rate used to account for the Company’s finance lease under ASC 842 is the Company’s estimated incremental borrowing rate of 7.11%. The Company is obligated to make five annual payments of $59,632 for an aggregate purchase price of $298,160. In addition, the Company exchanged certain of its current laboratory equipment as additional consideration. During the six months ended June 30, 2019, the Company made principal payments of $59,632 in connection with this leasing arrangement.
The following table presents the aggregate lease maturities of our finance lease.
2020 | $ | 59,632 | ||
2021 | 59,632 | |||
2022 | 59,632 | |||
2023 | 59,633 | |||
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Total | 238,529 | |||
Less interest | (37,042) | |||
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Current and noncurrent finance lease liability | 201,487 | |||
Less: Current portion | (55,674) | |||
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Finance lease liability, net of current portion | $ | 145,813 | ||
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11
Neoleukin Therapeutics, Inc.
Notes to Unaudited Interim Financial Statements
(6) | Debt |
Convertible Promissory Notes
On December 14, 2018, the Company entered into a Note Purchase Agreement with certain investors, pursuant to which it agreed to issue Convertible Promissory Notes (the “Notes”) in an aggregate amount of up to $5.0 million. As of December 31, 2018, the Company had issued Notes having an aggregate value of $3.5 million. On January 29, 2019, the Note Purchase Agreement and the Notes were amended to increase the amount issuable under the Note Purchase Agreement to $7.0 million. The sale of the additional $3.5 million Notes was completed on February 11, 2019, of which $0.9 million in cash proceeds were from certain of the Company’s founders, chief executive officer and family members.
Interest is payable on the Notes at a rate of 4.0%, compounded annually. For the six months ended June 30, 2019, the Company recognizednon-cash interest expense of $126,948.
The Notes also contain a most favored nation clause precluding the Company from offering convertible securities containing terms more favorable than those in the Notes without also offering such terms to the holders of the Notes. Both principal and interest on the Notes become due and payable on December 31, 2021 (the “Maturity Date”), unless the Notes are earlier converted under the terms and provisions set forth below.
Pursuant to the terms and provisions of the Note Purchase Agreement and the Notes, the Notes automatically convert into shares of the Company’s capital stock upon (i) a financing in which the Company sells shares of its preferred stock for a minimum of $10.0 million (a “Qualified Financing”) or (ii) the Company entering into a partnership agreement pursuant to which it would receive proceeds of at least $10.0 million within 12 months of the consummation of such agreement (a “Qualified Partnership Agreement”). The terms of the Notes also permit the holders of the Notes to voluntarily convert their Notes upon (i) a financing in which the Company sells shares of its preferred stock for aggregate proceeds between $5.0 million and $10.0 million (a“Non-Qualified Financing”); (ii) the Company entering into a partnership agreement pursuant to which it would receive proceeds between $5.0 million and $10.0 million within 12 months of the consummation of such agreement (a“Non-Qualified Partnership Agreement”) or (iii) the Maturity Date.
Upon the occurrence of a Qualified Financing, each holder of a Note would be entitled to receive that number of shares of the Company’s capital stock being sold in the Qualified Financing equal to the outstanding balance of such holder’s Note divided by the lower of (i) 80% of the purchase price of the preferred stock being sold in such Qualified Financing and (ii) the amount determined by dividing $25.0 million by the Company’s fully diluted capitalization outstanding immediately prior to the closing of the Qualified Financing.
Upon the occurrence of a Qualified Partnership Agreement, each holder of a Note would be entitled to receive that number of shares of the Company’s common stock equal to the outstanding balance of such holder’s Note divided by the amount determined by dividing $25.0 million by the Company’s fully diluted capitalization outstanding immediately prior to the execution of the Qualified Partnership Agreement.
Upon the occurrence of aNon-Qualified Financing, each holder of a Note would be entitled to receive that number of shares of the Company’s capital stock being sold in theNon-Qualified Financing equal to the outstanding balance of such holder’s Note divided by 90% of the purchase price of the preferred stock being sold in suchNon-Qualified Financing.
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Neoleukin Therapeutics, Inc.
Notes to Unaudited Interim Financial Statements
Upon the occurrence of aNon-Qualified Partnership Agreement, each holder of a Note would be entitled to receive that number of shares of the Company’s common stock equal to the outstanding balance of such holder’s Note divided by the amount determined by dividing by $20.0 million by the Company’s fully diluted capitalization outstanding immediately prior to the execution of theNon-Qualified Partnership Agreement.
Should the holder of a Note elect to convert his or her Note on the Maturity Date, then such holder would receive that number of shares of the Company’s common stock equal to the outstanding balance of such holder’s Note divided by the amount determined by dividing $25.0 million by the Company’s fully diluted capitalization outstanding on the Maturity Date.
If, prior to the conversion or maturity of the Notes, the Company consummates a change of control transaction, then upon the closing of such change of control transaction, the Company shall pay to each holder of a Note an amount equal to the greater of (i) the outstanding balance plus one times the original purchase price of the Note and (ii) the amount that would be received if the Note were converted into common stock immediately prior to the closing of the transaction at a fully diluted valuation of the Company equal to $25.0 million.
Management evaluated certain conversion features that result in the issuance of a variable number of shares as redemption features. These redemption features require bifurcation to which the Company determined the realization of such redemption features to be remote at the time of original issuance and at June 30, 2019.
In July 2019, the Note Purchase Agreement and Notes were further amended to address the conversion of the Notes should the Company enter into an agreement and plan of merger with Aquinox. Pursuant to the updated terms of the Note Purchase Agreement and the Notes, in the event that the Merger Agreement is executed prior to the conversion or maturity of the Notes, then immediately prior to such execution, the balance of each Note shall automatically convert into that number of shares of the Company’s common stock equal to the balance of the Note divided by the amount determined by dividing $25.0 million by the Company’s fully diluted capitalization outstanding immediately prior to the execution of the Merger agreement.
In August 2019, all outstanding principal and accrued interest under the Convertible Promissory Notes were converted (Note 10).
13
Neoleukin Therapeutics, Inc.
Notes to Unaudited Interim Financial Statements
(7) | Commitments and Contingency |
Licensing Option Agreement
On November 29, 2018, the Company entered into an Exclusive Option Agreement with the University of Washington (the “Option Agreement”), pursuant to which the Company was granted an exclusive option (the “Option”) to negotiate with the University of Washington to obtain an exclusive, royalty bearing license to certain intellectual property owned by the University of Washington (the “License”).
In consideration for the Option, the Option Agreement required the Company to reimburse the University of Washington for all expenses incurred in relation to the application for, and prosecution and maintenance of, any patents related to the License through the term of the Option Agreement and through any negotiations for a final license agreement.
The Company exercised its Option on January 30, 2019, and a negotiated term sheet setting forth the material terms of the proposed license agreement was accepted on April 4, 2019. The final license agreement was executed on July 8, 2019 (see Note 10).
Research and Development Arrangements
In the course of normal business operations, the Company enters into agreements with contract research organizations, or CROs, to assist in the performance of research and development and preclinical activities and contract manufacturers to assist with supply, manufacturing and controls (CMC) related expenses. Expenditures to CROs and contract manufacturers may represent a significant cost in preclinical and clinical development for the Company in future periods. The Company may elect to discontinue the work under these agreements at any time. The Company may also enter into additional collaborative research, contract research, manufacturing, and supplier agreements in the future, which may require upfront payments and long-term commitments of cash.
Employment Agreements
The Company entered into employment agreements with key personnel providing for compensation and severance in certain circumstances, as defined in the respective employment agreements. In addition, the agreements may include commitments to issue equity awards upon approval by the Company’s Board of Directors.
14
Neoleukin Therapeutics, Inc.
Notes to Unaudited Interim Financial Statements
Equity Incentive Plan
In 2018, the Company adopted its 2018 Equity Incentive Plan (2018 Plan). The total number of shares authorized under the 2018 Plan was 500,000. Eligible participants include employees, directors, and consultants. The 2018 Plan permits the granting of incentive stock options,non-statutory stock options, restricted stock, restricted stock units, and stock appreciation rights. The form and terms of any awards under the 2018 Plan are determined by the Company’s Board of Directors. There were no awards issued during the period from June 4, 2018 (inception) through June 30, 2019.
Litigation
Liabilities for loss contingencies arising from claims, assessments, litigation, fines, penalties, and other sources are recorded when it is probable that a liability has been incurred and the amount can be reasonably estimated. There are no such matters currently outstanding.
Operating Lease
In December 2018, the Company entered into a lease for office and laboratory facilities in Seattle, Washington. The lease commenced in January 2019 and expires in December 2019. The future minimum rental payments for fiscal 2019 will be $94,294. Rent expense for the six months ended June 30, 2019 was $54,551.
(8) | Stockholders’ Deficiency |
Common Stock
During the period from June 4, 2018 (inception) through June 30, 2019, the Company issued an aggregate of 9,500,000 shares to its founders and certain other parties pursuant to restricted stock purchase agreements. Shares issued pursuant to such agreements are subject to vesting periods ranging from immediate to 48 months. In the event an employee or consultant terminates their employment or relationship with the Company prior to completion of any applicable vesting period, the Company has the right to repurchase any unvested shares at their original purchase price. Proceeds received from unvested shares are recorded within other liabilities and reclassified into stockholders’ deficiency as they vest. As of June 30, 2019, there were 4,220,382 unvested shares subject to repurchase. Immediately prior to the consummation of the merger with Aquinox (Note 10), all unvested shares were vested and all repurchase rights held by the Company lapsed.
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, as may be declared by the Board of Directors, if any. No dividends have been declared through June 30, 2019.
15
Neoleukin Therapeutics, Inc.
Notes to Unaudited Interim Financial Statements
(9) | Related Party Transactions |
The Company issued convertible promissory notes (Note 6) in exchange for cash proceeds. During the period from June 4, 2018 (inception) through June 30, 2019, the Company received $7.0 million in cash proceeds from the issuance of convertible promissory notes, of which $3.6 million in cash proceeds were from certain of the Company’s founders, chief executive officer and family members.
As of June 30, 2019 and December 31, 2018, there were outstanding payables of approximately $2,000 and $46,000, respectively, to certain of the Company’s founders for expenses incurred and paid on the Company’s behalf.
(10) | Subsequent Events |
The Company has evaluated subsequent events from the balance sheet date through October 10, 2019, the date at which the unaudited interim financial statements were available to be issued, and there are no other items requiring disclosure except for the following:
Acquisition of Company
In August 2019, Aquinox completed its acquisition of the Company, and Apollo Sub, Inc., a Delaware corporation and wholly-owned subsidiary of Aquinox (“Merger Sub”), in accordance with the terms of the Agreement and Plan of Merger, dated as of August 5, 2019 (the “Merger Agreement”). Pursuant to the Merger Agreement, the Merger Sub merged with and into the Company (the “Merger”), with the Company surviving the Merger as a wholly-owned subsidiary of Aquinox.
Pursuant to the Merger Agreement, Aquinox issued to the former holders of the Company’s capital stock (i) 4,589,771 shares of Aquinox common stock representing approximately 19.5% of Aquinox’s issued and outstanding shares of common stock (calculated prior to the issuance of those new shares of common stock) and (ii) 101,927 shares of a newly created Aquinoxnon-voting convertible preferred stock that, following approval of Aquinox’s stockholders, will be convertible into 10,192,700 shares of Aquinox common stock such that following such conversion, the former holders of the Company’s capital stock will, together with the shares of common stock issued, hold in aggregate approximately 38.58% of the fully diluted outstanding shares of Aquinox. Any outstanding shares of the Company’s common stock that were unvested or subject to repurchase or forfeiture restrictions became fully vested and any repurchase or forfeiture restrictions thereon lapsed. Upon completion of the merger, Aquinox was renamed Neoleukin Therapeutics, Inc. and is trading under the new ticker symbol “NLTX” on the Nasdaq Global Market.
Upon consummation of the Merger, all outstanding principal and accrued interest under the Convertible Promissory Notes (Note 6) were converted into 2,901,245 shares of the Company’s common stock.
Licensing Agreement with University of Washington
In July 2019, the Company entered into an Exclusive License Agreement with the University of Washington, or UW, under which UW (on behalf of itself and Stanford University) granted the Company an exclusive worldwide license under certain patent rights, to make, have made, use, offer to sell, sell, offer to lease or lease, import, export or otherwise offer to dispose of licensed products in all fields of use, and a nonexclusive
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Neoleukin Therapeutics, Inc.
Notes to Unaudited Interim Financial Statements
worldwide license to use certainknow-how. The foregoing licenses are sublicensable by the Company without UW’s consent, subject to certain limited conditions.
As consideration for the licensed rights, the Company issued 531,579 shares of common stock to UW, representing five percent of the Company’s fully diluted capitalization on the date on which the Exclusive License Agreement was executed. In addition, the Company agreed to issue additional shares of common stock to UW sufficient to ensure UW owns an aggregate of five percent of the Company’s fully-diluted shares through such time as the Company completes an offering of equity securities issued for cash, in an amount equal to or exceeding $2.0 million; provided, however, that the UW shall not receive anti-dilution protection for equity capital raised in excess of $2.0 million. Pursuant to the agreement, the Company also granted to UW an assignable right to participate in any future sale of equity securities by the Company, subject to certain exclusions. The Company will owe UW: (i) an annual maintenance fee starting in January 2022 (but excluding any year in which minimum annual royalties are paid); (ii) up to $0.9 million in combined development and regulatory milestone payments with respect to each distinct class of licensed product; (iii) up to $10.0 million in combined commercial milestone payments based on cumulative net sales of licensed products within each distinct class of licensed products, beginning when cumulative net sales of the class of licensed products equals or exceeds $100.0 million, with the majority payable when cumulative net sales of the class of licensed products equals or exceeds $1.0 billion; (iv) a low single-digit royalty on net sales of licensed products sold by the Company and its sublicensees, which may be subject to reductions, and subject to minimum annual royalty payments following the first commercial sale of a licensed product; (v) a certain percentage of any sublicense consideration (other than royalties) the Company receives from sublicensees, ranging from 50% to low single-digit percentages based on the stage of development at the time the sublicense is executed; and (vi) a certain percentage of consideration the Company receives from an acquisition of the Company or its assets, ranging from 50% to zero based on the stage of development at the relevant time. The Company is obligated to pay royalties on acountry-by-country basis until the expiration of the last valid claim within the licensed patent rights in such country.
The agreement will expire upon the expiration of the last valid claim within the licensed patent rights. The Company may terminate the agreement upon prior written notice to UW. UW may terminate the agreement by a specified number of days’ notice if the Company permanently ceases operations, becomes insolvent or similar, or if the Company challenges the validity of the licensed patent rights. In addition, UW may terminate the agreement for material breach that is not cured within a specified number of days, which cure period is to be at least doubled if the Company is proceeding diligently to cure the default.
Common Stock Issuance
In July 2019, the Company issued 100,000 shares of its common stock to an affiliate of UW in the form of a donation.
Operating Lease
On September 26, 2019, the Company entered into a lease agreement for the lease of office space in Seattle, Washington, for the Company’s future principal executive offices, a laboratory for research and development and related uses. The lease was effective on September 23, 2019, commenced on October 1, 2019 and expires on September 30, 2021, unless terminated earlier. The Company will be obligated to pay approximately $358,000 in annual basic rent for the first year of the lease, and approximately $366,000 in the second year. The Company will also be responsible for the payment of additional rent to cover the Company’s share of the annual operating and tax expenses and utilities costs for the building.
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