季報
季度報告
10-Q
2026-08-06
Voyager Therapeutics次季虧損收窄至2450萬美元 現金儲備充足支持12個月營運
AI 繁中摘要
Voyager Therapeutics(納斯達克代號:VYGR)公布截至2026年6月30日第二季度及上半年業績(10-Q文件),公司為一間專注神經系統疾病基因療法及生物製劑的生物科技企業,目前仍在研發階段,未有產品收入。
財務重點(未經審計):
• 第二季度合作收入為320萬美元,上半年累計580萬美元;去年同期分別為520萬美元及1,170萬美元,收入下跌主要與Neurocrine及Novartis合作項目的確認時點有關。
• 第二季度研發費用2,200萬美元,上半年4,660萬美元;對比去年同期分別為3,130萬美元及6,290萬美元,反映公司控制成本及優先投放資源的策略。
• 第二季度一般及行政費用750萬美元,上半年1,580萬美元,按年均見下降。
• 第二季度淨虧損2,450萬美元,每股虧損0.40美元;上半年淨虧損5,240萬美元,每股虧損0.87美元。去年同期淨虧損分別為3,340萬美元及6,440萬美元,虧損幅度明顯收窄。
• 截至2026年6月30日,現金、現金等價物及有價證券合共1.488億美元(其中現金及現金等價物3,580萬美元、有價證券1.13億美元)。管理層表示現有資金足以支持至少未來十二個月的營運開支及資本開支。
研發及業務進展:
• 阿爾茨海默病抗tau抗體項目VY7523正進行第一期多次遞增劑量臨床試驗,計劃於2026年第四季度公佈早期阿爾茨海默病患者初步數據。
• Tau基因沉默療法VY1706預計於2026年第四季度啟動臨床試驗並開始為患者用藥,初期急性安全性數據預計於2027年初公佈,腦脊液tau生物標誌物相關數據則料於2027年下半年公佈。
• 公司繼續與Neurocrine、Novartis及Alexion(AstraZeneca Rare Disease)等夥伴合作,亦與Transition Bio合作開發針對TDP-43的小分子藥物,用於肌萎縮側索硬化症及額顳葉癡呆症。
• 研發平台方面,TRACER™ AAV衣殼發現平台及非病毒載體平台Voyager NeuroShuttle™持續推進。
其他事項:
• 公司透過「按市價發售」協議在期內發行普通股集資約570萬美元(扣除發行成本),有助延長現金跑道。
• 截至2026年6月30日,累計虧損為4.983億美元;公司仍在虧損狀態,預期需繼續依賴股權融資、合作里程碑及成本分攤支持營運。
• 期內並無重大訴訟或或然負債;租賃及轉租安排維持正常。
對投資者的潛在影響:
公司第二季度虧損較去年收窄,加上現金儲備充足,短期財務壓力可控。市場焦點將落在VY7523及VY1706兩項臨床數據讀出時間,尤其VY7523第四季度數據可望成為股價催化劑。但需注意臨床開發失敗風險、合作收入波動及持續融資需要,投資者宜審慎評估風險回報。
展開英文正文
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Table of Contents UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 10-Q ☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the quarterly period ended June 30, 2026 ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from ______ to ______ Commission file number: 001-37625 Voyager Therapeutics, Inc. (Exact name of Registrant as specified in its charter) Delaware 46-3003182 (State or other jurisdiction of incorporation or organization) (I.R.S. Employer Identification No.) 75 Hayden Avenue, Lexington, Massachusetts 02421 (Address of principal executive offices) (Zip Code) (857) 259-5340 (Registrant’s telephone number, including area code) Not Applicable (Former name, former address and former fiscal year, if changed since last report) Securities registered pursuant to Section 12(b) of the Act: Title of each class Trading Symbol(s) Name of each exchange on which registered Common Stock, $0.001 par value VYGR Nasdaq Global Select Market 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. Yes No ☐ Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes No ☐ Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act. Large accelerated filer ☐ Accelerated filer ☒ Non-accelerated 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. ☐ Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ☐ No ☒ The number of outstanding shares of the registrant’s common stock, par value $0.001 per share, as of July 30, 2026, was 61,617,948. Table of Contents Forward-Looking Statements This Quarterly Report on Form 10-Q contains forward-looking statements that involve substantial risks and uncertainties. All statements other than statements of historical facts contained in this Quarterly Report on Form 10-Q, including statements regarding our strategy, future operations, future financial position, future revenue, projected costs, prospects, plans, objectives of management and expected market growth, are forward-looking statements. These statements involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. The words “anticipate,” “believe,” “estimate,” “expect,” “intend,” “may,” “might,” “plan,” “predict,” “project,” “target,” “potential,” “contemplate,” “goals,” “will,” “would,” “could,” “should,” “continue,” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. These forward-looking statements include, among other things, statements about: •our plans to develop, manufacture and commercialize our proprietary adeno-associated virus, or AAV, gene therapy, antibody, non-viral therapeutic, and small molecule product candidates; •our ability to continue to develop our proprietary gene therapy platform technologies, including our TRACERTM (Tropism Redirection of AAV by Cell-type-specific Expression of RNA) discovery platform, our non-viral therapeutics platform, including VOYAGER NEUROSHUTTLETM, and our proprietary antibody, small molecule, gene therapy, shuttled or vectorized antibody, and non-viral therapeutic programs; •our ability to identify and optimize product candidates, proprietary AAV capsids, and non-viral blood-brain-barrier shuttles; •our strategic collaborations and licensing agreements with, and funding from, our collaboration partners Neurocrine Biosciences, Inc. and Novartis Pharma AG and our licensee Alexion, AstraZeneca Rare Disease (successor-in-interest to former licensee Pfizer Inc.); •our collaboration with Transition Bio, Inc. to advance small molecules targeting TDP-43 to treat amyotrophic lateral sclerosis and frontotemporal dementia with TDP-43 pathology; •our ongoing and planned clinical trials, preclinical development efforts, related timelines and studies, including our plans to generate initial data from the Phase 1 multiple ascending dose clinical trial of VY7523 in early Alzheimer’s disease patients in the fourth quarter of 2026 and to initiate and begin dosing patients in a clinical trial of VY1706 in the fourth quarter of 2026 and generate initial acute safety data and initial cerebrospinal fluid tau biomarker-based data in early 2027 and the second half of 2027, respectively; •our ability to enter into future collaborations, strategic alliances, or option and license arrangements; •the timing of and our ability to submit applications and obtain and maintain regulatory approvals for our product candidates, including the ability to submit investigational new drug applications for our programs; •our belief as to potential outcomes of our clinical development activities, and plans and potential outcomes with respect to interactions with regulatory authorities; •our estimates regarding future revenue, expenses, contingent liabilities, existing cash resources, capital requirements and cash runway; •our intellectual property position and our ability to obtain, maintain and enforce intellectual property protection for our proprietary assets; •our estimates regarding the size of the potential markets for our product candidates and our ability to serve those markets; •our need for and the timing of additional funding and our plans and ability to raise additional capital, including through equity offerings, debt financings, collaborations, strategic alliances, and option and license arrangements; 2 Table of Contents •our competitive position and the success of competing products that are or might become available for the indications that we are pursuing; •the impact of government laws and regulations, including in the United States, the European Union, and other important geographies such as Japan; and •our ability to control costs and prioritize our product candidate pipeline and platform development objectives successfully in connection with our strategic initiatives. These forward-looking statements are only predictions, and we may not actually achieve the plans, intentions or expectations disclosed in our forward-looking statements. You should not place undue reliance on our forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in the forward-looking statements we make. We have based these forward-looking statements largely on our current expectations and projections about future events and trends that we believe may affect our business, financial condition and operating results. We have included important factors in the cautionary statements included in our Annual Report on Form 10-K filed with the Securities and Exchange Commission on March 9, 2026, particularly in “Part I, Item 1A — Risk Factors,” and, if applicable, this Quarterly Report on Form 10-Q, particularly in “Part II, Item 1A — Risk Factors,” that could cause actual future results or events to differ materially from the forward-looking statements that we make. Our forward-looking statements do not reflect the potential impact of any future acquisitions, mergers, dispositions, strategic collaborations, licenses, joint ventures or investments we may make or enter into. You should read this Quarterly Report on Form 10-Q and the documents that we have filed as exhibits to this Quarterly Report on Form 10-Q with the understanding that our actual future results may be materially different from what we expect. We do not assume any obligation to update any forward-looking statements whether as a result of new information, future events or otherwise, except as required by applicable law. We obtained the statistical and other industry and market data in this Quarterly Report on Form 10-Q and the documents we have filed as exhibits to this Quarterly Report on Form 10-Q from our own internal estimates and research, as well as from industry and general publications and research, surveys, studies and trials conducted by third parties. Some data is also based on our good faith estimates, which are derived from management’s knowledge of the industry and independent sources. This data involves a number of assumptions and limitations, and you are cautioned not to give undue weight to such estimates. In addition, while we believe the market opportunity information included in this Quarterly Report on Form 10-Q and the documents we have filed as exhibits to this Quarterly Report on Form 10-Q is reliable and is based upon reasonable assumptions, such data involves risks and uncertainties and are subject to change based on various factors, including those discussed under “Risk Factors” and in the documents we have filed as exhibits to the Quarterly Report on Form 10-Q. In addition, statements that “we believe” and similar statements reflect our beliefs and opinions on the relevant subject. These statements are based upon information available to us as of the date of this Quarterly Report on Form 10-Q, and while we believe such information forms a reasonable basis for such statements, such information may be limited or incomplete, and our statements should not be read to indicate that we have conducted an exhaustive inquiry into, or review of, all potentially available relevant information. These statements are inherently uncertain, and investors are cautioned not to unduly rely upon these statements. We own various U.S. federal trademark registrations and applications and unregistered trademarks, including our corporate logo. This Quarterly Report on Form 10-Q and the documents filed as exhibits to this Quarterly Report on Form 10-Q contain references to trademarks, service marks and trade names referred to in this Quarterly Report on Form 10-Q and the information incorporated herein, including logos, artwork, and other visual displays, that may appear without the ® or TM symbols, but such references are not intended to indicate, in any way, that we will not assert, to the fullest extent under applicable law, our rights or the rights of the applicable licensor to these trademarks, service marks or trade names. We do not intend our use or display of other companies’ trade names, service marks or trademarks to imply a relationship with, or endorsement or sponsorship of us by, any other companies. All trademarks, service marks and trade names included or incorporated by reference into this Quarterly Report on Form 10-Q and the documents filed as exhibits to this Quarterly Report on Form 10-Q are the property of their respective owners. 3 Table of Contents VOYAGER THERAPEUTICS, INC. FORM 10-Q TABLE OF CONTENTS Page PART I. FINANCIAL INFORMATION ITEM 1. CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) CONDENSED CONSOLIDATED BALANCE SHEETS 5 CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS 6 CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY 7 CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS 8 NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS 9 ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS 18 ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK 32 ITEM 4. CONTROLS AND PROCEDURES 32 PART II. OTHER INFORMATION ITEM 1. LEGAL PROCEEDINGS 33 ITEM 1A. RISK FACTORS 33 ITEM 5. OTHER INFORMATION 33 ITEM 6. EXHIBITS 34 SIGNATURES 35 4 Table of Contents PART I. FINANCIAL INFORMATION Voyager Therapeutics, Inc. Condensed Consolidated Balance Sheets (amounts in thousands, except share and per share data) (unaudited) June 30, December 31, 2026 2025 Assets Current assets: Cash and cash equivalents $ 35,769 $ 65,300 Marketable securities 80,569 131,147 Accounts receivable 2,932 1,761 Related party collaboration receivable 222 151 Prepaid expenses and other current assets 5,736 4,328 Total current assets 125,228 202,687 Property and equipment, net 11,194 13,136 Restricted cash 2,736 2,736 Marketable securities, non-current 32,476 5,244 Other non-current assets 214 — Operating lease, right-of-use assets 25,905 28,478 Total assets $ 197,753 $ 252,281 Liabilities and stockholders’ equity Current liabilities: Accounts payable $ 1,614 $ 5,013 Accrued expenses 7,951 12,098 Operating lease liabilities 6,876 7,840 Deferred revenue 244 1,590 Total current liabilities 16,685 26,541 Operating lease liabilities, net of current portion 25,691 28,659 Other non-current liabilities 1,000 1,000 Total liabilities 43,376 56,200 Commitments, contingencies, and other liabilities (see note 7) Stockholders’ equity: Preferred stock, $0.001 par value: 5,000,000 shares authorized at June 30, 2026 and December 31, 2025; no shares issued and outstanding at June 30, 2026 and December 31, 2025 — — Common stock, $0.001 par value: 240,000,000 and 120,000,000 shares authorized at June 30, 2026 and December 31, 2025, respectively; 61,273,390 and 59,047,860 shares issued and outstanding at June 30, 2026 and December 31, 2025, respectively 61 59 Additional paid-in capital 653,052 641,895 Accumulated other comprehensive (loss) income (421 ) 32 Accumulated deficit (498,315 ) (445,905 ) Total stockholders’ equity 154,377 196,081 Total liabilities and stockholders’ equity $ 197,753 $ 252,281 The accompanying notes are an integral part of these condensed consolidated financial statements. 5 Table of Contents Voyager Therapeutics, Inc. Condensed Consolidated Statements of Operations and Comprehensive Loss (amounts in thousands, except share and per share data) (unaudited) Three Months Ended Six Months Ended June 30, June 30, 2026 2025 2026 2025 Collaboration revenue $ 3,165 $ 5,200 $ 5,758 $ 11,673 Operating expenses: Research and development 22,041 31,330 46,643 62,856 General and administrative 7,516 10,495 15,777 20,135 Total operating expenses 29,557 41,825 62,420 82,991 Operating loss (26,392 ) (36,625 ) (56,662 ) (71,318 ) Other income, net: Interest income 1,528 2,831 3,440 6,122 Other income 411 427 846 845 Total other income, net 1,939 3,258 4,286 6,967 Loss before income taxes (24,453 ) (33,367 ) (52,376 ) (64,351 ) Income tax provision 20 15 34 52 Net loss $ (24,473 ) $ (33,382 ) $ (52,410 ) $ (64,403 ) Other comprehensive (loss) income: Net unrealized (loss) gain on available-for-sale securities (158 ) (22 ) (453 ) 186 Total other comprehensive (loss) income (158 ) (22 ) (453 ) 186 Comprehensive loss $ (24,631 ) $ (33,404 ) $ (52,863 ) $ (64,217 ) Net loss per share, basic and diluted $ (0.40 ) $ (0.57 ) $ (0.87 ) $ (1.10 ) Weighted-average common shares outstanding, basic and diluted 60,547,863 58,666,460 60,025,001 58,508,989 The accompanying notes are an integral part of these condensed consolidated financial statements. 6 Table of Contents Voyager Therapeutics, Inc. Condensed Consolidated Statements of Stockholders’ Equity (amounts in thousands, except share data) (unaudited) Accumulated Additional Other Common Stock Paid-In Comprehensive Accumulated Stockholders' Shares Amount Capital Loss Deficit Equity Balance at December 31, 2025 59,047,860 $ 59 $ 641,895 $ 32 $ (445,905 ) $ 196,081 Exercises of stock options 87,081 — 294 — — 294 Vesting of restricted stock units 545,015 — — — — — Issuance of common stock from at-the-market sales agreement, net of issuance costs 630,570 1 3,037 — — 3,038 Stock-based compensation expense — — 2,488 — — 2,488 Unrealized loss on available-for-sale securities, net of tax — — — (295 ) — (295 ) Net loss — — — — (27,937 ) (27,937 ) Balance at March 31, 2026 60,310,526 $ 60 $ 647,714 $ (263 ) $ (473,842 ) $ 173,669 Exercises of stock options 105,481 — 57 — — 57 Vesting of restricted stock units 55,914 — — — — — Issuance of common stock under ESPP 73,473 — 219 — — 219 Issuance of common stock from at-the-market sales agreement, net of issuance costs 727,996 1 2,629 — — 2,630 Stock-based compensation expense — — 2,433 — — 2,433 Unrealized loss on available-for-sale securities, net of tax — — — (158 ) — (158 ) Net loss — — — — (24,473 ) (24,473 ) Balance at June 30, 2026 61,273,390 $ 61 $ 653,052 $ (421 ) $ (498,315 ) $ 154,377 Accumulated Additional Other Common Stock Paid-In Comprehensive Accumulated Stockholders' Shares Amount Capital Loss Deficit Equity Balance at December 31, 2024 54,731,316 $ 55 $ 626,296 $ (407 ) $ (326,184 ) $ 299,760 Exercises of stock options 27,613 — 82 — — 82 Vesting of restricted stock units 450,556 — — — — — Stock-based compensation expense — — 3,673 — — 3,673 Unrealized gain on available-for-sale securities, net of tax — — — 208 — 208 Net loss — — — — (31,021 ) (31,021 ) Balance at March 31, 2025 55,209,485 $ 55 $ 630,051 $ (199 ) $ (357,205 ) $ 272,702 Exercises of stock options 27,433 1 78 — — 79 Vesting of restricted stock units 99,528 — — — — — Issuance of common stock under ESPP 98,510 — 434 — — 434 Stock-based compensation expense — — 4,133 — — 4,133 Unrealized loss on available-for-sale securities, net of tax — — — (22 ) — (22 ) Net loss — — — — (33,382 ) (33,382 ) Balance at June 30, 2025 55,434,956 $ 56 $ 634,696 $ (221 ) $ (390,587 ) $ 243,944 The accompanying notes are an integral part of these condensed consolidated financial statements. 7 Table of Contents Voyager Therapeutics, Inc. Condensed Consolidated Statements of Cash Flows (amounts in thousands) (unaudited) Six Months Ended June 30, 2026 2025 Cash flow from operating activities Net loss $ (52,410 ) $ (64,403 ) Adjustments to reconcile net loss to net cash used in operating activities: Stock-based compensation expense 4,921 7,806 Depreciation 1,840 2,079 Amortization of premiums and discounts on marketable securities (613 ) (1,789 ) Loss on disposal of fixed assets 105 79 Non-cash lease expense 2,573 2,376 Changes in operating assets and liabilities: Accounts receivable (1,171 ) (170 ) Related party collaboration receivable (71 ) (175 ) Prepaid expenses and other current assets (1,397 ) (1,826 ) Other non-current assets (214 ) — Accounts payable (3,399 ) (2,192 ) Accrued expenses (4,147 ) (2,146 ) Operating lease liabilities (3,932 ) (3,522 ) Deferred revenue (1,346 ) (7,273 ) Net cash used in operating activities (59,261 ) (71,156 ) Cash flow from investing activities Purchases of property and equipment (14 ) (1,763 ) Purchases of marketable securities (70,851 ) (114,790 ) Proceeds from sales and maturities of marketable securities 94,357 159,687 Net cash provided by investing activities 23,492 43,134 Cash flow from financing activities Proceeds from the exercise of stock options 351 161 Proceeds from the purchase of common stock under ESPP 219 434 Proceeds from the issuance of common stock from at-the-market sales agreement, net of issuance costs 5,668 — Net cash provided by financing activities 6,238 595 Net decrease in cash, cash equivalents, and restricted cash (29,531 ) (27,427 ) Cash, cash equivalents, and restricted cash, beginning of period 68,036 74,241 Cash, cash equivalents, and restricted cash, end of period $ 38,505 $ 46,814 The accompanying notes are an integral part of these condensed consolidated financial statements. 8 Table of Contents VOYAGER THERAPEUTICS, INC. NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS 1. Nature of business Voyager Therapeutics, Inc. (the “Company”) is a biotechnology company whose mission is to leverage the power of human genetics to modify the course of and ultimately cure neurological diseases. Its pipeline includes programs for Alzheimer’s disease, Friedreich’s ataxia, Parkinson’s disease, and multiple other diseases of the central nervous system (“CNS”). Its pipeline includes programs it wholly owns and programs it is advancing with licensees and collaborators, including Alexion, AstraZeneca Rare Disease; Novartis Pharma AG (“Novartis”); Neurocrine Biosciences, Inc. (“Neurocrine”); and Transition Bio, Inc. Many of the Company’s programs are derived from its TRACER™ (Tropism Redirection of AAV by Cell-type-specific Expression of RNA) adeno-associated virus (“AAV”) capsid discovery platform, which it has used to generate novel capsids and identify associated receptors to potentially enable high brain penetration with genetic medicines following intravenous dosing. TRACER is a broadly applicable, RNA-based screening platform that enables rapid discovery of AAV capsids with robust penetration of the blood-brain barrier (“BBB”) and enhanced CNS tropism in multiple species, including non-human primates. The Company is also developing a second, non-viral therapeutics platform focused on non-viral receptor-mediated transport across the BBB, the Voyager NeuroShuttleTM platform. The Company has a history of incurring annual net operating losses. As of June 30, 2026, the Company had an accumulated deficit of $498.3 million. The Company has not generated any product revenue and has financed its operations primarily through public offerings and private placements of its equity securities and funding from fees, milestone payments, and cost reimbursements associated with its prior and current collaborations and license agreements. As of June 30, 2026, the Company had cash, cash equivalents, and marketable securities of $148.8 million. Based upon its current operating plan, the Company expects that its existing cash, cash equivalents, and marketable securities at June 30, 2026, to be sufficient to meet the Company’s planned operating expenses and capital expenditure requirements for at least twelve months from the issuance of these condensed consolidated financial statements. There can be no assurance that the Company will be able to obtain additional debt or equity financing on terms acceptable to the Company or generate product revenue or revenue from collaboration partners, on a timely basis or at all. The failure of the Company to obtain sufficient funds on acceptable terms when needed could have a material adverse effect on the Company’s business, results of operations, and financial condition and require the Company to defer or limit some or all of its research, development and/or clinical programs. 2. Summary of significant accounting policies and basis of presentation Basis of Presentation The accompanying unaudited condensed consolidated financial statements of the Company have been prepared in accordance with accounting principles generally accepted in the United States (“GAAP”) for interim financial reporting. Accordingly, they do not include all of the information and footnotes required by GAAP for complete financial statements. For further information, refer to the consolidated financial statements and footnotes included in the Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2025, as filed with the Securities and Exchange Commission on March 9, 2026. These interim condensed consolidated financial statements, in the opinion of management, reflect all normal recurring adjustments necessary for a fair presentation of the Company’s financial position and results of operations for the periods presented. Any reference in these notes to applicable guidance is meant to refer to the authoritative GAAP, which can be found in the Accounting Standards Codification and Accounting Standards Updates of the Financial Accounting Standards Board. Principles of Consolidation The unaudited interim condensed consolidated financial statements include the accounts of the Company and its wholly-owned subsidiary as disclosed in Note 2, Summary of Significant Accounting Policies and Basis of Presentation, within the “Notes to Consolidated Financial Statements” accompanying the Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2025. Intercompany balances and transactions have been eliminated. 9 Table of Contents Use of Estimates The preparation of condensed consolidated financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the amounts reported in the condensed consolidated financial statements and accompanying notes. On an ongoing basis, the Company’s management evaluates its estimates, which include, but are not limited to, estimates related to revenue recognition, research and development accrued expenses, stock‑based compensation expense, and income taxes. The Company bases its estimates on historical experience and other market-specific or other relevant assumptions that it believes to be reasonable under the circumstances. Actual results may differ from those estimates or assumptions. Summary of Significant Accounting Policies There have been no changes in the Company’s significant accounting policies as described in Note 2, Summary of Significant Accounting Policies and Basis of Presentation, within the “Notes to Consolidated Financial Statements” accompanying the Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2025. 3. Fair value measurements Assets and liabilities measured at fair value on a recurring basis as of June 30, 2026 and December 31, 2025, are as follows: Quoted Prices Significant in Active Other Significant Markets for Observable Unobservable Identical Assets Inputs Inputs Assets Total (Level 1) (Level 2) (Level 3) June 30, 2026 (in thousands) Cash equivalents: Money market funds $ 24,548 $ 24,548 $ — $ — Marketable securities: U.S. Treasury notes 39,931 39,931 — — U.S. Government agency securities 23,940 23,940 — — Corporate bonds 43,371 — 43,371 — Commercial paper 5,803 — 5,803 — Total cash equivalents and marketable securities $ 137,593 $ 88,419 $ 49,174 $ — December 31, 2025 Cash equivalents: Money market funds $ 51,161 $ 51,161 $ — $ — Commercial paper 3,477 — 3,477 — Marketable securities: U.S. Treasury notes 72,805 72,805 — —