-
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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(Address of principal executive offices) | (Zip Code) |
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(Registrant's telephone number, including area code)
Securities registered pursuant to Section 12(b) of the Act:
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Title of each class | Trading Symbol(s) | on which registered | ||
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.
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 (§232.0405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files).
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.
Accelerated filer ☐ | |
Non-accelerated filer ☐ | Smaller reporting company |
Emerging growth company |
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. ☐
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As of May 5, 2023, the registrant had
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 strategic reset and building a pipeline of clinically differentiated, high-value medicines, including the potential benefits and clinical opportunity for our current pipeline candidates; |
● | the timing of and costs or charges associated with our reductions in force and license agreement terminations, wind downs of partnerships and programs, and the savings benefits we expect to receive, and effects on our cash burn; |
● | our plans to separate out our immune-inflammatory (I&I) assets, including formation of a new subsidiary and seeking capital therefor; |
● | clinical trial timelines and plans for our pipeline candidates, including initiation and enrollment; |
● | our ability to find a commercialization partner for aumolertinib; |
● | the success, costs and timing of our product development activities; |
● | our ability to obtain and maintain regulatory approval for our products, and any related restrictions and limitations on any approved product; |
● | our ability to locate and acquire products or product candidates and integrate those into our business; |
● | our ability to maintain our existing or enter into additional license agreements, particularly in light of the termination of two of our previous license agreements, and the risk of delays or unforeseen costs in terminating such arrangements; |
● | our ability to adapt our initial commercial and pricing models, plans and strategies following our strategic reset; |
● | our ability to maintain our existing or enter into additional drug engineering collaborations, particularly in light of our plans to terminate the development of certain programs; |
● | our ability to maintain our existing or enter into additional manufacturing agreements; |
● | our ability to compete with other companies currently marketing or engaged in the development of innovative drug candidates, many of which have greater financial and marketing resources than we do; |
● | the size and growth potential of the markets for our products, and our ability to serve those markets, either alone or in partnership with others; |
● | changes in applicable laws or regulations; |
● | our ability to raise capital in the future; |
● | our estimates regarding expenses, future revenue, capital requirements and needs for additional financing; |
● | our financial performance; |
● | our ability to compete effectively in a competitive industry; |
● | our ability to protect and enhance our corporate reputation and brand; |
● | expectations concerning our relationships and actions with third parties; |
● | potential liquidity and trading of our securities; |
● | our ability to attract and retain qualified directors, officers, employees and other key personnel; |
● | our ability to grow and manage growth profitably and retain our key employees, particularly in light of |
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the two reductions in force that we have announced this year; and |
● | the impact of the ongoing COVID-19 pandemic, along with any other health pandemics or global events, such as the Russian invasion of Ukraine, or recent bank failures. |
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 of 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 that we currently deem immaterial, and these additional risks could also materially impair our business, operations or market price of our securities.
● | We do not have any products approved for commercial sale and have not generated any revenue to date, and so may never become profitable. |
● | We have provided notices to terminate our license agreements with CStone Pharmaceuticals (CStone) and Lynk Pharmaceutical (Hangzhou) Co., Ltd. (Lynk) and, accordingly, are no longer seeking regulatory approval for sugemalimab, nofazinlimab, or EQ121 in any jurisdiction, and we are also exploring commercialization partnerships for aumolertinib. We may make similar decisions for other pipeline candidates, indications, and/or markets, which will impact the revenues we may generate from our pipeline candidates when and if approved. |
● | Our decision to separate our I&I programs into a new subsidiary may not provide the expected benefits, and we may not be successful in developing those programs as a separate business. |
● | In jurisdictions in which regulators do not solely accept data from our licensing partners from other countries but instead require additional data generated from additional preclinical studies and clinical trials as a basis for regulatory approvals (such as the U.S. Food and Drug Administration (FDA)), we will incur additional costs and experience delays in completing, or ultimately may be unable to complete, the development of such product candidate; we may also choose not to pursue development for certain indications in that market given the potentially increased costs or delays, or impact on our ability to complete the development of such product candidate (such as our recent decision to terminate our license agreements with CStone for sugemalimab and nofazinlimab, and Lynk for EQ121 and our earlier decisions not to seek FDA approval of sugemalimab in Stage IV non-small cell lung cancer (NSCLC) or extranodal NK/T-cell lymphoma (ENKTL)). |
● | Drug development is a lengthy, expensive and uncertain process. We may incur additional costs or experience delays in completing, or ultimately be unable to complete, the development of a product candidate. Even if we achieve positive clinical trial results, there is no guarantee that our product |
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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 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. 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. |
● | We are now focused on building a pipeline of clinically differentiated, high-value medicines and may not be successful in adapting our mission and initial business model following our recent strategic reset. |
● | We may be unsuccessful in achieving broad market awareness and acceptance or changing prescribing or purchasing habits of healthcare system participants or keeping up to date with recent developments in the medical field regarding treatment options. |
● | We may be unable to continue to attract, acquire and retain third-party collaborators, particularly as we adapt our initial commercial and pricing models, plans and strategies, or we may fail to do so in an effective manner. Our collaborations with third parties are also subject to certain risks. |
● | Our financial projections are subject to significant risks, assumptions, estimates and uncertainties, and our actual results may differ materially. |
● | Our current or future 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 (or our collaboration and license partners, as applicable) are unable to obtain and maintain patent and other intellectual property protection for our technology and 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 successfully commercialize our technology and drugs may be impaired. |
● | Our failure to manage growth effectively could cause our business to suffer and have an adverse effect on our ability to execute our business strategy, as well as on our operating results and financial condition. |
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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)
March 31, | 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 12) |
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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) |
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| ( | ||
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 | ||||||
March 31, | ||||||
| 2023 |
| 2022 | |||
Operating expenses: | ||||||
Research and development | $ | | $ | | ||
General and administrative | | | ||||
Restructuring (note 7) | | — | ||||
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 income (expense), net | ( | | ||||
Total other income, net | | | ||||
Net income (loss) | $ | ( | $ | | ||
Other comprehensive income (loss), net of tax: | ||||||
Foreign currency translation adjustments | | | ||||
Unrealized holding gains on short-term investments | | — | ||||
Comprehensive income (loss), net of tax | $ | ( | $ | | ||
Net income (loss) per share - basic | $ | ( | $ | | ||
Net income (loss) per share - diluted | $ | ( | $ | | ||
Weighted average common shares outstanding - basic | | | ||||
Weighted average common shares outstanding - 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 |
| — |
| — |
| |
| — | — |
| | ||||||
Unrealized holding gains on short-term investments, net of tax of $ | — | — | — | | — | | |||||||||||
Net loss |
| — |
| — |
| — |
| — | ( |
| ( | ||||||
Balance at March 31, 2023 |
| | $ | | $ | | $ | | $ | ( | $ | | |||||
Balance at December 31, 2021 | | | | | ( | $ | | ||||||||||
Vesting of restricted common stock |
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| — |
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| — |
| — |
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Common stock issued upon exercise of stock options |
| | — |
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| — |
| — |
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Foreign currency translation adjustment, net of tax of $ |
| — |
| — |
| — |
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| — |
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Stock-based compensation |
| — |
| — |
| |
| — |
| — |
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Net income |
| — |
| — |
| — |
| — |
| |
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Balance at March 31, 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)
| Three months ended | |||||
March 31, | ||||||
2023 |
| 2022 | ||||
Operating activities: |
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Net income (loss) | $ | ( | $ | | ||
Reconciliation of net income (loss) to net cash used in operating activities: |
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Stock-based compensation | |
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Depreciation expense | |
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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 | ( |
| ( | |||
Accounts payable | |
| ( | |||
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 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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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’s lead product candidate, lerociclib, is a novel, oral, and selective small molecule cyclin-dependent kinase (CDK) 4/6 inhibitor in development for use in combination with endocrine therapy. The lead indications being explored are hormone receptor positive (HR+)/human epidermal growth factor receptor 2 negative (HER2-) metastatic breast cancer (mBC) and first-line treatment of advanced/metastatic or recurrent low grade endometrioid endometrial cancer (mEC). In addition, EQRx continues to advance its early-stage research and development programs through collaborations with leading drug engineering companies, with a focus on assets with clear potential for market-leading differentiation.
Risks and Uncertainties
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. Product candidates in-licensed and to be in-licensed, discovered alone or in partnership, acquired or developed will require significant research and development efforts, including 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 and reporting capabilities.
There can be no assurance that the Company’s ability to identify product candidates and subsequently research and develop those product candidates will be successfully completed, that adequate protection for the Company’s intellectual property will be obtained both inside and outside the United States, that any products developed will obtain necessary government regulatory approval, or that any approved products will be commercially viable. Even if the Company’s product identification and development efforts are successful, it is uncertain when, if ever, the Company will generate significant revenue, if any, from product sales, and the Company may be subject to significant competitive or litigation risks.
Liquidity
The Company has limited operating history and anticipates that it will incur losses for the foreseeable future as it builds its internal infrastructure, identifies and acquires product candidates, conducts the research and development of its product candidates, and seeks marketing approval for its late-stage programs. The Company incurred a net loss of $
As of March 31, 2023, the Company had cash, cash equivalents, short-term investments and restricted cash of $
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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 an immaterial wholly-owned 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 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 March 31, 2023, its results of operations for the three months ended March 31, 2023 and 2022 and cash flows for the three months ended March 31, 2023 and 2022. The results of operations for the three months ended March 31, 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 of research and development and manufacturing expenses, stock-based compensation expense, 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 March 31, 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.
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March 31, | ||||||
| 2023 |
| 2022 | |||
Cash and cash equivalents | $ | | $ | | ||
Restricted cash |
| |
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Total cash, cash equivalents and restricted cash | $ | | $ | |
4. BUSINESS COMBINATION
Summary of 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 “Merger Agreement”), by and among the former EQRx, Inc. (“Legacy EQRx”), CMLS III and Clover III Merger Sub, Inc. (“Merger Sub”). As contemplated by the Merger Agreement, 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 “Business Combination”). As a result of the Business Combination, CMLS III was renamed EQRx, Inc., and Legacy EQRx was renamed EQRx International, Inc.
The Company assumed
In connection with the 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 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 Business Combination, net of transaction costs paid as of the Closing Date |
| |
Less transaction costs paid following the Closing Date |
| ( |
Net proceeds from the 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
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common stock if at any time between the
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 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 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 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 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):
| March 31, 2023 | |||||||||||
Level 1 |
| Level 2 |
| Level 3 |
| Total | ||||||
Assets |
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Cash equivalents: |
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Money market funds |
| $ | |
| $ | — |
| $ | — |
| $ | |
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 |
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Contingent earn-out liability | $ | — | $ | — | $ | | $ | | ||||
Warrant liabilities |
| |
| |
| — |
| | ||||
Total financial liabilities | $ | | $ | | $ | | $ | |
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| December 31, 2022 | |||||||||||
Level 1 |
| Level 2 |
| Level 3 |
| Total | ||||||
Assets |
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Cash equivalents: |
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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 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:
| March 31, | December 31, | ||||
2023 | 2022 | |||||
Market price of public stock |
| $ | |
| $ | |
Expected share price volatility |
|
| ||||
Risk-free interest rate |
|
| ||||
Estimated dividend yield |
|
|
13
The change in the fair value of the contingent earn-out liabilities during the three months ended March 31, 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 March 31, 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):
| March 31, 2023 | |||||||||||
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 | $ | | $ | | $ | ( | $ | |
| 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
14
7. ACCRUED EXPENSES
Accrued expenses consisted of the following (in thousands):
March 31, | December 31, | |||||
2023 | 2022 | |||||
External research and development |
| $ | |
| $ | |
Accrued compensation |
| |
| | ||
Accrued professional services |
| |
| | ||
Accrued consulting |
| |
| | ||
Restructuring | | — | ||||
Other |
| |
| | ||
Total accrued expenses | $ | | $ | |
In February 2023, the Company announced a reduction in force to further increase operational efficiencies and streamline expenses. As a result, the Company recognized a charge for employee-related termination costs in the first quarter of 2023 of $
8. WARRANTS
CMLS III issued the Public Warrants and Private Warrants, which have an exercise price of $
Subsequent to the Business Combination, the Public Warrants and Private Warrants met liability classification requirements because the Warrants contain provisions whereby adjustments to the settlement amount of the Warrants are based on a variable that is not an input to the fair value of a “fix-for-fixed” option and the existence of the potential for net cash settlement for the Warrant holders in the event of a tender offer. In addition, the Private Warrants are potentially subject to a different settlement amount depending upon the holder of the Private Warrants, which precludes them from being considered indexed to the entity’s own stock. Therefore, the Warrants were classified as liabilities on the Company’s condensed consolidated balance sheets at March 31, 2023 and December 31, 2022. As of March 31, 2023,
As of March 31, 2023, the following Warrants were outstanding:
Warrant Type |
| Shares |
| Exercise Price | |
Public Warrants |
| | $ | | |
Private Warrants |
| | $ | | |
Total Warrants |
| |
|
|
Public Warrants
Redemption of Warrants When the Price per Share of Common Stock Equals or Exceeds $
The Company may redeem the outstanding Warrants:
● | in whole and not in part; |
● | at a price of $ |
● | upon not less than |
15
● | if, and only if, the last reported sale price of the common stock for any |
Redemption of Warrants When the Price per Share of Common Stock Equals or Exceeds $
The Company may redeem the outstanding Warrants:
● | in whole and not in part; |
● | at $ |
● | if, and only if, the Reference Value equals or exceeds $ |
● | if the Reference Value is less than $ |
The “fair market value” of the common stock shall mean the volume weighted average price of the common stock during the
No fractional shares will be issued upon exercise of the Warrants.
Private Warrants
The Private Warrants are identical to the Public Warrants, except that the Private Warrants and the common stock issuable upon the exercise of the Private Warrants were not transferable, assignable or saleable until
The Private Warrants and the Public Warrants contain provisions that require them to be classified as derivative liabilities in accordance with ASC 815. Accordingly, at the end of each reporting period, changes in fair value during the period are recognized as a change in fair value of warrant liabilities within the condensed consolidated statements of operations and comprehensive income (loss). The Company adjusts the warrant liability for changes in the fair value until the earlier of (a) the exercise or expiration of the Warrants or (b) the redemption of the Warrants, at which time the Warrants will be reclassified to additional paid-in capital.
Derivative Warrant liabilities are classified as non-current liabilities, as their liquidation is not reasonably expected to require the use of current assets or require the creation of current liabilities.
The Warrants were valued on March 31, 2023 and December 31, 2022 using the listed trading price of $
16
9. STOCKHOLDERS’ EQUITY
Preferred Stock
Upon closing of the Business Combination, pursuant to the terms of its Amended and Restated Certificate of Incorporation, the Company became authorized to issue
Common Stock
Upon the closing of the Business Combination, pursuant to the terms of the Company’s Amended and Restated Certificate of Incorporation, the Company became authorized to issue
Each share of common stock entitles the holder to
As of March 31, 2023,
10. STOCK-BASED COMPENSATION
In January 2020, Legacy EQRx’s board of directors and stockholders adopted the 2019 Stock Option and Grant Plan (the “2019 Plan”), which was assumed in the Business Combination. On December 16, 2021, the Company’s board of directors and its stockholders adopted the 2021 Option Grant and Incentive Plan (the “2021 Plan”), which became effective upon the closing of the Business Combination. The 2021 Plan provides for the issuance of incentive stock options, non-qualified stock options, restricted stock awards, unrestricted stock awards, restricted stock units, or any combination of the foregoing to employees, board members, consultants and advisors.
Upon completion of the Business Combination, the Company ceased issuing awards under the 2019 Plan. The total number of shares of common stock that may be issued under the 2021 Plan was
17
Stock-based compensation expense included in the Company’s condensed consolidated statements of operations and comprehensive income (loss) was as follows (in thousands):
Three months ended March 31, | ||||||
2023 |
| 2022 | ||||
Stock options, restricted stock units and restricted common stock | $ | | $ | | ||
Earn-Out Shares | | | ||||
Total stock-based compensation | $ | | $ | | ||
Research and development | $ | |
| $ | | |
General and administrative |
| |
| | ||
Restructuring | ( | — | ||||
Total stock-based compensation | $ | | $ | |
Stock Options
A summary of stock option activity for employee and nonemployee awards during the three months ended March 31, 2023 is presented below:
Weighted | ||||||||||
Average | Aggregate | |||||||||
Weighted- | Remaining | Intrinsic | ||||||||
Average | Contractual | Value | ||||||||
Exercise | Term | (in | ||||||||
| Options |
| Price |
| (years) |
| thousands) | |||
Outstanding at December 31, 2022 | | $ | | |||||||
Granted | — | — | ||||||||
Exercised | ( | | ||||||||
Cancelled/forfeited | ( | | ||||||||
Outstanding at March 31, 2023 |
| | $ | |
| $ | |