-
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM
QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For the quarterly period ended
or
TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For the transition period fromto
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Securities registered pursuant to Section 12(b) of the Act:
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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.
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TABLE OF CONTENTS
In this Quarterly Report on Form 10-Q, unless otherwise stated or as the context otherwise requires, references to “EQRx,” “the Company,” “we,” “us,” “our” and similar references refer to EQRx, Inc. together with its consolidated subsidiaries.
The EQRx logo and other trademarks or service marks of EQRx appearing in this Quarterly Report on Form 10-Q are the property of EQRx. This Quarterly Report on Form 10-Q may also contain registered marks, trademarks and trade names of other companies, all of which are the property of their respective holders.
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CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
This Quarterly Report on Form 10-Q contains forward-looking statements within the meaning of Section 27A of the Securities Act, and Section 21E of the Exchange Act. We have based these forward-looking statements on our current expectations and projections about future events. In some cases, you can identify forward-looking statements by terminology such as “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “might,” “plan,” “possible,” “potential,” “predict,” “project,” “should,” “will,” “would” or the negative of such terms or other similar expressions. All statements, other than statements of present or historical fact included in this Quarterly Report on Form 10-Q, that relate to our future financial performance, strategy, expansion plans, future operations, future operating results, estimated revenues, losses, projected costs, prospects, plans and objectives of management are forward-looking statements. Any statements that refer to projections, forecasts or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking statements.
Forward-looking statements in this Quarterly Report on Form 10-Q may include, for example, statements about:
● | our plans and expectations regarding the proposed acquisition of our company (the Merger) by Revolution Medicines, Inc. (Revolution Medicines) in an all stock transaction pursuant to that certain Agreement and Plan of Merger dated July 31, 2023 by and among our company, Revolution Medicines and the merger subsidiary parties thereto (the Merger Agreement); |
● | our undertakings with respect to our product portfolio and collaboration arrangements in the Merger Agreement, including the timing of and costs or charges associated with our reductions in force and license agreement terminations, and wind-downs of partnerships and programs, including terminating or opting out of certain research and development (R&D) programs, as well as the associated effects on our cash burn; and |
● | our ability to continue as a stand-alone business if the proposed Merger is not successful, including the need to rebuild our business, pursue an alternative transaction or the potential dissolution and liquidation of our company. |
These forward-looking statements represent our plans, objectives, estimates, expectations and intentions only as of the date of this filing. You should read this report completely and with the understanding that our actual future results and the timing of events may be materially different from what we expect, and we cannot otherwise guarantee that any forward-looking statement will be realized. We hereby qualify all of our forward-looking statements by these cautionary statements.
Except as required by law, we undertake no obligation to update or supplement any forward-looking statements publicly, or to update or supplement the reasons that actual results could differ materially from those anticipated in these forward-looking statements, even if new information becomes available in the future. You are advised, however, to consult any further disclosures we make on related subjects.
SUMMARY OF RISK FACTORS
Our business involves significant risks. Below is a summary of the material risks that our business faces, which makes an investment in our securities speculative and risky. This summary does not address all these risks. These risks are more fully described under the heading “Risk Factors” in Part I, Item 1A of our Annual Report on Form 10-K for the year ended December 31, 2022 as filed with the Securities and Exchange Commission on February 23, 2023 as supplemented by the risks described under “Risk Factors” in Part II, Item 1A in this Quarterly Report on Form 10-Q. Before making investment decisions regarding our securities, you should carefully consider these risks. The occurrence of any of the events or developments described below could have a material adverse effect on our business, results of operations, financial condition, prospects and stock price. In such event, the market price of our securities could decline, and you could lose all or part of your investment. Further, there are additional risks not described below that are either not currently known to us or
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that we currently deem immaterial, and these additional risks could also materially impair our business, operations or the market price of our securities.
● | The announcement and pendency of the Merger could adversely affect our business, prospects, financial condition, and results of operations. |
● | While the Merger Agreement is in effect, we are subject to restrictions on our business activities, including an obligation to use reasonable best efforts to conduct our business consistent with a mutually agreed operating and capital expenditure budget. Moreover, pursuant to the Merger Agreement, we have agreed to take steps to wind down and terminate our current product pipeline and other R&D activities, which will have consequences for our business, financial condition and results of operations should the proposed Merger not be consummated. |
● | The Merger Agreement contains provisions that could discourage a potential competing acquirer of our company or could result in any competing proposal being at a lower price than it might otherwise be. |
● | Litigation against us, Revolution Medicines, or the members of our respective boards or management teams, could prevent or delay the completion of the Merger. |
● | The Merger may not be completed within the expected timeframe, or at all, and significant delay or the failure to complete the Merger could adversely affect our business and the market price of our common stock. |
● | If the Merger is not consummated by 12:00 a.m. Eastern Time on January 31, 2024, either we or Revolution Medicines may terminate the Merger Agreement, subject to certain exceptions. |
● | If the Merger is not consummated, our board of directors may decide to pursue a dissolution and liquidation. In such an event, the amount of cash available for distribution to our stockholders will depend heavily on the timing of such liquidation as well as the amount of cash that will need to be reserved for commitments and contingent liabilities. |
● | If the Merger is not consummated, and we attempt to rebuild our drug development business activities, we may be unable to attract, acquire and retain third-party collaborators, particularly as we recently took steps or are taking steps to terminate or opt-out of our existing collaborations, or we may fail to do so in an effective manner. |
● | We had previously terminated our license agreements with CStone Pharmaceuticals (Cstone) and Lynk Pharmaceutical (Hangzhou) Co., Ltd. (Lynk), recently provided notices to terminate our license agreements with G1 Therapeutics, Inc. (G1) and Hansoh (Shangai) Healthtech Co. Ltd. and Jiangsu Hansoh Pharmaceutical Group Company Ltd. (collectively, Hansoh) pursuant to the Merger Agreement, and have taken or plan to take steps to terminate or opt-out of our discovery collaboration agreements; accordingly, we are no longer seeking regulatory approval nor actively developing any pipeline candidates as we pursue the Merger. |
● | We do not have any products approved for commercial sale and have not generated any revenue to date. Given the wind-down of our programs as described herein, if the Merger is consummated, we do not expect that we will ever become profitable as a stand-alone business. If the Merger is not consummated and we determine whether to rebuild our portfolio or pursue an alternative transaction, there is no guarantee we will succeed in such efforts. |
● | Drug development is a lengthy, expensive and uncertain process. If the Merger is not consummated, and we attempt to rebuild a product pipeline following our planned wind-down of our existing pipeline pursuant to the Merger Agreement, we may incur additional costs or experience delays in completing, or ultimately be unable to complete, the development of a product candidate. Additionally, we may have difficulty entering into new relationships and agreements with licensing partners, other collaborators, and other relevant third parties following the planned termination of our existing relationships. Even if we are successful in establishing such new relationships and achieve positive clinical trial results, there is no guarantee that any product candidates will be approved. Our competitors may also obtain FDA or other regulatory approval for their products sooner than we may obtain approval for ours and for multiple indications in parallel, which could require us to undertake additional trials and also result in our competitors establishing a strong market position before we or our collaborators are able to enter the market. If we experience delays in obtaining data from our licensing partners, their other licensees or other collaborators, or other relevant third parties, or we experience delays or difficulties in the initiation or enrollment of our clinical trials, our receipt of necessary regulatory approvals could be |
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delayed or prevented. |
● | We have never successfully completed the regulatory approval process for any of our product candidates, and we may be unable to do so for any product candidates, particularly after the wind-down of our existing programs pursuant to the Merger Agreement. Even if we are successful in obtaining regulatory approval in one indication or jurisdiction for a product candidate, it does not guarantee that we will be able to obtain pricing or reimbursement approval in such jurisdiction, that our products will be broadly adopted in such jurisdiction, or that we will be able to obtain regulatory approval in any other indication or jurisdiction. Further, even if we receive regulatory approval for any of our current or future product candidates, we will be subject to ongoing obligations and continued regulatory review, which may result in significant additional expense. |
● | Our financial projections are subject to significant risks, assumptions, estimates and uncertainties, and our actual results may differ materially. |
● | Any product candidates may cause adverse or other undesirable side effects that could delay or prevent their regulatory approval, limit the commercial profile of an approved label, or result in significant negative consequences following marketing approval, if any. |
● | If we attempt to rebuild a development pipeline, and we (or our future collaboration and license partners, as applicable) are unable to obtain and maintain patent and other intellectual property protection for our technology and any product candidates, or if the scope of the intellectual property protection obtained is not sufficiently broad, our competitors could develop and commercialize technology and drugs similar or identical to ours, and our ability to rebuild a development pipeline of and/or successfully commercialize our future technology and drugs may be impaired. |
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PART I – FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS
EQRx, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(unaudited)
(in thousands, except share and per share information)
June 30, | December 31, | |||||
| 2023 |
| 2022 | |||
Assets |
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Current assets: |
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Cash and cash equivalents |
| $ | | $ | | |
Short-term investments | | | ||||
Prepaid expenses and other current assets |
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Total current assets |
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Property and equipment, net |
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Restricted cash |
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Right-of-use asset |
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Other investments |
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Other non-current assets |
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Total assets | $ | | $ | | ||
Liabilities and Stockholders’ Equity |
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Current liabilities: |
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Accounts payable | $ | | $ | | ||
Accrued expenses |
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Lease liability, current |
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Total current liabilities |
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Non-current liabilities: |
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Contingent earn-out liability |
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Warrant liabilities |
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Lease liability, non-current |
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Restricted stock repurchase liability |
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Total liabilities |
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Commitments and contingencies (note 13) |
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Stockholders' equity: |
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Preferred stock, $ | ||||||
Common stock, $ |
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Additional paid-in capital |
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Accumulated other comprehensive income (loss) |
| |
| ( | ||
Accumulated deficit |
| ( |
| ( | ||
Total stockholders’ equity |
| |
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Total liabilities and stockholders’ equity | $ | | $ | |
See accompanying notes to the condensed consolidated financial statements.
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EQRx, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE INCOME (LOSS)
(unaudited)
(in thousands, except share and per share information)
| Three months ended | Six months ended | ||||||||||
June 30, | June 30, | |||||||||||
| 2023 |
| 2022 |
| 2023 |
| 2022 | |||||
Operating expenses: |
| |||||||||||
Research and development | $ | | $ | | $ | | $ | | ||||
General and administrative | | | | | ||||||||
Restructuring | | — | | — | ||||||||
Total operating expenses | | | | | ||||||||
Loss from operations | ( | ( | ( | ( | ||||||||
Other income (expense): | ||||||||||||
Change in fair value of contingent earn-out liability | | ( | | | ||||||||
Change in fair value of warrant liabilities | | | | | ||||||||
Interest income, net | | | | | ||||||||
Other expense, net | ( | ( | ( | ( | ||||||||
Total other income (expense), net | | ( | | | ||||||||
Net loss | $ | ( | $ | ( | $ | ( | $ | ( | ||||
Other comprehensive income (loss), net of tax: | ||||||||||||
Foreign currency translation adjustments | | | | | ||||||||
Unrealized holding gains (losses) on short-term investments | | ( | | ( | ||||||||
Comprehensive loss, net of tax | $ | ( | $ | ( | $ | ( | $ | ( | ||||
Net loss attributable to common stockholders - basic and diluted | ( | ( | ( | ( | ||||||||
Net loss per share - basic and diluted | ( | ( | ( | ( | ||||||||
Weighted average common shares outstanding - basic and diluted | | | | |
See accompanying notes to the condensed consolidated financial statements.
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EQRx, INC.
CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY
(unaudited)
(in thousands, except share information)
Accumulated Other | |||||||||||||||||
Common Stock | Additional Paid-in | Comprehensive | Accumulated | Total Stockholders’ | |||||||||||||
Shares |
| Amount |
| Capital |
| Income (Loss) |
| Deficit |
| Equity | |||||||
Balance at December 31, 2022 |
| | $ | | $ | | $ | ( | $ | ( |
| $ | | ||||
Vesting of restricted common stock | | — | | — | — | | |||||||||||
Common stock issued upon exercise of stock options |
| | — |
| |
| — | — |
| | |||||||
Foreign currency translation adjustment, net of tax of $ |
| — |
| — |
| — |
| | — |
| | ||||||
Stock-based compensation |
| — |
| — |
| |
| — | — |
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Unrealized holding gains on short-term investments, net of tax of $ | — | — | — | | — | | |||||||||||
Net loss |
| — |
| — |
| — |
| — | ( |
| ( | ||||||
Balance at March 31, 2023 |
| | $ | | $ | | $ | | $ | ( | $ | | |||||
Vesting of restricted common stock | | — | | — | — | | |||||||||||
Common stock issued upon exercise of stock options |
| | — |
| |
| — | — |
| | |||||||
Foreign currency translation adjustment, net of tax of $ |
| — |
| — |
| — |
| | — |
| | ||||||
Stock-based compensation |
| — |
| — |
| |
| — | — |
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Unrealized holding gains on short-term investments, net of tax of $ | — | — | — | | — | | |||||||||||
Net loss |
| — |
| — |
| — |
| — | ( |
| ( | ||||||
Balance at June 30, 2023 |
| | $ | | $ | | $ | | $ | ( | $ | | |||||
Balance at December 31, 2021 | | | | | ( | $ | | ||||||||||
Vesting of restricted common stock |
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| — |
| |
| — |
| — |
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Common stock issued upon exercise of stock options |
| | — |
| |
| — |
| — |
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Foreign currency translation adjustment, net of tax of $ |
| — |
| — |
| — |
| |
| — |
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Stock-based compensation |
| — |
| — |
| |
| — |
| — |
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Net income |
| — |
| — |
| — |
| — |
| |
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Balance at March 31, 2022 |
| | $ | | $ | | $ | | $ | ( | $ | | |||||
Vesting of restricted common stock |
| |
| — |
| |
| — |
| — |
| | |||||
Common stock issued upon exercise of stock options |
| | — |
| |
| — |
| — |
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Foreign currency translation adjustment, net of tax of $ |
| — |
| — |
| — |
| |
| — |
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Stock-based compensation |
| — |
| — |
| |
| — |
| — |
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Unrealized holding losses on short-term investments, net of tax of $ | — | — | — | ( | ( | ||||||||||||
Net loss |
| — |
| — |
| — |
| — |
| ( |
| ( | |||||
Balance at June 30, 2022 |
| | $ | | $ | | $ | ( | $ | ( | $ | |
See accompanying notes to the condensed consolidated financial statements.
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EQRx, INC.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(unaudited)
(in thousands)
| Six months ended | |||||
June 30, | ||||||
2023 |
| 2022 | ||||
Operating activities: |
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Net loss | $ | ( | $ | ( | ||
Reconciliation of net loss to net cash used in operating activities: |
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Stock-based compensation | |
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Depreciation expense | |
| | |||
Net amortization of premiums and discounts on investments | ( | ( | ||||
Change in fair value of contingent earn-out liability | ( |
| ( | |||
Change in fair value of warrant liabilities | ( |
| ( | |||
Non-cash lease expense | ( |
| ( | |||
Changes in operating assets and liabilities: | ||||||
Prepaid expenses and other assets | |
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Accounts payable | ( |
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Accrued expenses | |
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Net cash used in operating activities |
| ( |
| ( | ||
Investing activities: |
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Purchases of property and equipment | ( |
| ( | |||
Purchases of investments | ( | ( | ||||
Proceeds from maturities of investments | | — | ||||
Net cash used in investing activities |
| ( |
| ( | ||
Financing activities: |
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Transaction costs paid in connection with December 2021 Business Combination and PIPE Financing | — |
| ( | |||
Proceeds from the exercise of stock options | |
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Net cash provided by (used in) financing activities | |
| ( | |||
Decrease in cash, cash equivalents and restricted cash | ( |
| ( | |||
Cash, cash equivalents and restricted cash, beginning of period |
| |
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Cash, cash equivalents and restricted cash, end of period | $ | | $ | | ||
Supplemental disclosure of non-cash activities |
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Receivable due from stock option exercises | $ | — | $ | | ||
Purchases of property and equipment in accounts payable | $ | — | $ | |
See accompanying notes to the condensed consolidated financial statements.
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EQRx, INC.
Notes to the Condensed Consolidated Financial Statements
1. NATURE OF BUSINESS
EQRx, Inc. (“EQRx” or the “Company”) is a biopharmaceutical company committed to developing and commercializing innovative medicines for some of the most prevalent disease areas. The Company recently entered into the Merger Agreement (as defined below) and accordingly, has taken steps or is taking steps to wind down its product portfolio and research and development activities pursuant to the Merger Agreement. Accordingly, it is no longer pursuing any product candidates in active clinical development.
Proposed Acquisition by Revolution Medicines
On July 31, 2023, EQRx, Revolution Medicines, Inc., (“Revolution Medicines”), Equinox Merger Sub I, Inc., a direct, wholly owned subsidiary of Revolution Medicines (“Merger Sub I”), and Equinox Merger Sub II LLC, a direct, wholly owned subsidiary of Revolution Medicines (“Merger Sub II”), entered into an Agreement and Plan of Merger (the “Merger Agreement”). Pursuant to the Merger Agreement, and subject to the satisfaction or waiver of certain conditions, Merger Sub I will be merged with and into EQRx (the “First Merger”), with EQRx surviving the First Merger as a direct, wholly owned subsidiary of Revolution Medicines (the “Surviving Corporation”), and as soon as practicable following the First Merger, the Surviving Corporation will be merged with and into Merger Sub II, with Merger Sub II surviving as a direct, wholly owned subsidiary of Revolution Medicines (together with the First Merger, the “Mergers” or the “Merger”).
The boards of directors of each of EQRx and Revolution Medicines have approved the Merger Agreement and the transactions contemplated thereby. The EQRx board of directors’ approval was made upon the recommendation of a committee of independent directors.
At the effective time of the First Merger (the “Effective Time”), each share of common stock, par value $
The “Exchange Ratio” will be determined by dividing the aggregate number of shares of Parent Common Stock to be issued as Merger Consideration by the number of shares of EQRx Common Stock outstanding immediately prior to the Effective Time, determined in accordance with the Merger Agreement. The number of shares of EQRx Common Stock outstanding for purposes of determining the Exchange Ratio will (i) take into account the number of shares of EQRx Common Stock subject to EQRx in-the-money stock options, EQRx RSU awards and EQRx restricted stock awards that will convert into shares of Parent Common Stock in the Merger, (ii) include
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EQRx, Revolution Medicines, Merger Sub I and Merger Sub II each made certain representations, warranties and covenants in the Merger Agreement, including, among other things, covenants by EQRx to use reasonable best efforts to conduct its business consistent with a mutually agreed operating and capital expenditure budget and use commercially reasonable efforts to wind down certain mutually agreed programs, and to refrain from taking certain actions specified in the Merger Agreement.
The parties expect that the Merger will be completed in November 2023, subject to satisfaction of customary closing conditions, including approval by each of Revolution Medicines’ and EQRx’s stockholders.
Risks and Uncertainties
In addition to risks and uncertainties related to the Merger, including the risk that the Merger is not consummated, the Company is subject to risks and uncertainties common to companies in the biotechnology industry, including, but not limited to, identification of product candidates, development by competitors of new technological innovations, dependence on key personnel, protection of proprietary technology, compliance with government regulations, establishment of relationships with strategic partners, and the ability to secure additional capital to fund operations.
Liquidity
The Company has limited operating history and anticipates that it will incur losses for the foreseeable future, particularly if the proposed Merger is not successful and it attempts to rebuild its internal infrastructure, identify and acquire product candidates, conduct the research and development of its product candidates, and seek marketing approval therefor. The Company incurred a net loss of $
As of June 30, 2023, the Company had cash, cash equivalents, short-term investments and restricted cash of $
2. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Basis of Presentation
The accompanying condensed consolidated interim financial statements and accompanying notes include the accounts of the Company and its wholly-owned subsidiaries EQRx International, Inc., EQRx Securities Holding Corporation, and two immaterial wholly-owned subsidiaries, one of which is a foreign subsidiary. All intercompany transactions and balances have been eliminated in consolidation. The accompanying unaudited condensed consolidated interim financial statements have been prepared in accordance with accounting principles generally accepted in the United States (“GAAP”) for interim financial information. Any reference in these notes to applicable guidance is meant to refer to the authoritative GAAP as found in the Accounting Standards Codification (“ASC”).
Certain information and disclosures normally included in consolidated financial statements prepared in accordance with GAAP have been condensed or omitted. Accordingly, these condensed consolidated interim financial statements should be read in conjunction with the audited financial statements for the year ended December 31, 2022 and the related notes, which provide a more complete discussion of the Company’s accounting policies and certain other information. The December 31, 2022 condensed consolidated balance sheet was derived from the Company’s audited financial statements. These unaudited condensed consolidated interim financial statements have been prepared on the same basis as the annual consolidated financial
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statements and, in the opinion of management, reflect all adjustments, which include only normal recurring adjustments, necessary to present fairly the Company’s condensed consolidated financial position as of June 30, 2023, its results of operations for the three and six months ended June 30, 2023 and 2022 and cash flows for the six months ended June 30, 2023 and 2022. The results of operations for the three and six months ended June 30, 2023 are not necessarily indicative of the results to be expected for the year ending December 31, 2023, or for any other future annual or interim period.
Use of Estimates
The preparation of financial statements in accordance with GAAP requires management to make estimates and assumptions, based on judgments considered reasonable, which 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 expenses during the reporting period. The Company bases its estimates and assumptions on historical experience, known trends and events and various other factors that management believes to be 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. Significant estimates and assumptions reflected in these condensed consolidated financial statements include the accrual for research and development and manufacturing expenses, stock-based compensation expense, restructuring costs, the valuation of the contingent earn-out liability, and the fair value of private warrants. Changes in estimates are recorded in the period in which they become known. Due to the risks and uncertainties involved in the Company’s business and evolving market conditions and, given the subjective element of the estimates and assumptions made, actual results may differ from estimated results.
3. CASH, CASH EQUIVALENTS AND RESTRICTED CASH
The Company considers all highly liquid investments with an original or remaining maturity of three months or less at the date of purchase to be cash equivalents. Cash equivalents as of June 30, 2023 consisted of money market funds (see note 5).
Amounts included in restricted cash consist of cash held to collateralize a letter of credit issued as a security deposit in connection with the Company’s lease of its corporate facility located in Cambridge, MA.
The following table provides a reconciliation of cash, cash equivalents and restricted cash reported within the applicable condensed consolidated balance sheet that sums to the total of the same such amounts shown in the condensed consolidated statement of cashflows (in thousands):
June 30, | ||||||
| 2023 |
| 2022 | |||
Cash and cash equivalents | $ | | $ | | ||
Restricted cash |
| |
| | ||
Total cash, cash equivalents and restricted cash | $ | | $ | |
4. BUSINESS COMBINATION
Summary of December 2021 Business Combination
EQRx, Inc., formerly known as CM Life Sciences III Inc. (“CMLS III”), was incorporated in Delaware on January 25, 2021 for the purpose of effecting a merger, capital stock exchange, asset acquisition, stock purchase, reorganization or similar business combination with one or more businesses. On December 17, 2021 (the “Closing Date”), the Company consummated the merger transaction contemplated pursuant to a definitive merger agreement dated August 5, 2021 (the “DeSPAC Merger Agreement”), by and among the former EQRx, Inc. (“Legacy EQRx”), CMLS III and Clover III Merger Sub, Inc. (“SPAC Merger Sub”). As contemplated by the DeSPAC Merger Agreement, SPAC Merger Sub merged with and into Legacy EQRx, with Legacy EQRx surviving the merger as a wholly-owned subsidiary of CMLS III (such transactions, the “December 2021
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Business Combination”). As a result of the December 2021 Business Combination, CMLS III was renamed EQRx, Inc., and Legacy EQRx was renamed EQRx International, Inc.
The Company assumed
In connection with the December 2021 Business Combination, CMLS III entered into agreements with existing and new investors to subscribe for and purchase an aggregate of
Net Proceeds
In connection with the December 2021 Business Combination, the Company received net proceeds of $
Recapitalization | ||
Cash - CMLS III's trust account and cash (net of redemptions) | $ | |
Cash - PIPE Financing |
| |
Less transaction costs and fees paid as of the Closing Date |
| ( |
Proceeds from the December 2021 Business Combination, net of transaction costs paid as of the Closing Date |
| |
Less transaction costs paid following the Closing Date |
| ( |
Net proceeds from the December 2021 Business Combination | $ | |
Earn-Out Shares
Following the Closing Date, holders of Legacy EQRx securities and options (“Earn-Out Service Providers”) are entitled to receive as additional merger consideration up to
Earn-Out Shares allocated to Earn-Out Service Providers who held equity securities not subject to any vesting conditions or restrictions as of the Closing Date of the December 2021 Business Combination are accounted for in accordance with ASC Topic 815, Derivatives and Hedging (“ASC 815”), as the Earn-Out Shares are not indexed to the common stock. Pursuant to ASC 815, these Earn-Out Shares were accounted for as a liability at the Closing Date of the December 2021 Business Combination and subsequently remeasured at each reporting date with changes in fair value recorded as a component of other income (expense), net in the condensed consolidated statements of operations and comprehensive income (loss).
Earn-Out Shares allocated to Earn-Out Service Providers who held shares of common stock or options to purchase common stock that are subject to time-based vesting conditions or restrictions as of the Closing Date of the December 2021 Business Combination are accounted for in accordance with ASC Topic 718, Share-Based Compensation (“ASC 718”), as the Earn-Out Shares are subject to forfeiture based on the satisfaction
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of certain service conditions. Pursuant to ASC 718, these Earn-Out Shares were measured at fair value at the grant date (the Closing Date) and will be recognized as expense over the time-based vesting period with a credit to additional paid-in-capital.
5. FAIR VALUE MEASUREMENTS
Items Measured at Fair Value on a Recurring Basis
The following tables present information about the Company’s assets and liabilities that are measured at fair value on a recurring basis (in thousands):
| June 30, 2023 | |||||||||||
Level 1 |
| Level 2 |
| Level 3 |
| Total | ||||||
Assets |
|
|
|
|
|
|
|
| ||||
Cash equivalents: |
|
|
|
|
|
|
|
| ||||
Money market funds |
| $ | |
| $ | — |
| $ | — |
| $ | |
Commercial paper (due within 90 days) |
| — |
| |
| — |
| | ||||
U.S. agency securities (due within 90 days) | — | | — | | ||||||||
Investments: | ||||||||||||
U.S. agency securities (due within 1 year) | — | | — | | ||||||||
Commercial paper (due within 1 year) | — | | — | | ||||||||
Total financial assets | $ | | $ | | $ | — | $ | | ||||
Liabilities |
|
|
|
|
|
|
|
| ||||
Contingent earn-out liability | $ | — | $ | — | $ | | $ | | ||||
Warrant liabilities |
| |
| |
| — |
| | ||||
Total financial liabilities | $ | | $ | | $ | | $ | |
| December 31, 2022 | |||||||||||
Level 1 |
| Level 2 |
| Level 3 |
| Total | ||||||
Assets |
|
|
|
|
|
|
|
| ||||
Cash equivalents: |
|
|
|
|
|
|
|
| ||||
Money market funds |
| $ | |
| $ | — |
| $ | — |
| $ | |
Commercial paper (due within 90 days) |
| — |
| |
| — |
| | ||||
Investments: | ||||||||||||
U.S. treasury bills (due within 1 year) | — | | — | | ||||||||
U.S. agency securities (due within 1 year) | — | | — | | ||||||||
Commercial paper (due within 1 year) | — | | — | | ||||||||
Corporate notes (due within 1 year) | — | | — | | ||||||||
Total financial assets | $ | | $ | | $ | — | $ | | ||||
Liabilities |
|
|
|
|
|
|
|
| ||||
Contingent earn-out liability | $ | — | $ | — | $ | | $ | | ||||
Warrant liabilities |
| |
| |
| — |
| | ||||
Total financial liabilities | $ | | $ | | $ | | $ | |
In determining the fair value of its cash equivalents at each date presented above, the Company relied on quoted prices for similar securities in active markets or using other inputs that are observable or can be
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corroborated by observable market data. There were no changes in valuation techniques or transfers between fair value measurement levels for the periods presented.
The fair value of the Public Warrants was based on observable listed prices for such warrants. The fair value of the Private Warrants is equivalent to that of the Public Warrants as they have substantially the same terms; however, they are not actively traded.
The carrying amounts of the Company’s prepaid and other current assets, accounts payable and accrued liabilities, approximate fair value due to their short maturities.
Level 3 Financial Instruments
The Earn-Out Shares accounted for under ASC 815 are categorized as Level 3 fair value measurements within the fair value hierarchy because the Company estimates projections utilizing unobservable inputs. Contingent earn-out payments involve certain assumptions requiring significant judgment and actual results can differ from assumed and estimated amounts.
In determining the fair value of the contingent earn-out liabilities, the Company uses a Monte Carlo simulation model using a distribution of potential outcomes on a monthly basis prioritizing the more reliable information available. The assumptions utilized in the calculation are based on the achievement of certain stock price milestones, including the Company’s stock price at each reporting period, expected volatility, risk-free rate, expected term and expected dividend yield.
The Earn-Out Shares subject to liability accounting were valued using the following assumptions under the Monte Carlo simulation model:
| June 30, | December 31, | ||||
2023 | 2022 | |||||
Market price of public stock |
| $ | |
| $ | |
Expected share price volatility |
|
| ||||
Risk-free interest rate |
|
| ||||
Estimated dividend yield |
|
|
The change in the fair value of the contingent earn-out liabilities during the six months ended June 30, 2023 was as follows (in thousands):
| Fair Value | ||
Fair value as of December 31, 2022 |
| $ | |
Change in fair value of earn-out liability |
| ( | |
Fair value as of June 30, 2023 | $ | |
6. SHORT-TERM INVESTMENTS
The following tables summarize the amortized cost, gross unrealized gains, gross unrealized losses and fair value of available-for-sale investments by type of security (in thousands):
| June 30, 2023 | |||||||||||
Amortized Cost Basis |
| Unrealized Gains |
| Unrealized Losses |
| Fair Value | ||||||
Available-for-sale securities: |
|
|
|
| ||||||||
U.S. agency securities (due within 1 year) | | | ( | | ||||||||
Commercial paper (due within 1 year) | | | ( | | ||||||||
Total available-for-sale securities | $ | | $ | | $ | ( | $ | |
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| December 31, 2022 | |||||||||||
Amortized Cost Basis |
| Unrealized Gains |
| Unrealized Losses |
| Fair Value | ||||||
Available-for-sale securities: |
|
|
|
| ||||||||
U.S. treasury bills (due within 1 year) | $ | | $ | — | $ | ( | $ | | ||||
U.S. agency securities (due within 1 year) | | | — | | ||||||||
Commercial paper (due within 1 year) | | | ( | | ||||||||
Corporate notes (due within 1 year) | | — | ( | | ||||||||
Total available-for-sale securities | $ | | $ | | $ | ( | $ | |
There were
7. ACCRUED EXPENSES
Accrued expenses consisted of the following (in thousands):