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Corbus Pharmaceuticals Holdings, Inc.

For the period ended Sep 30, 2026. Filed Nov 10, 2026.

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A company's report for each of its first three quarters. The financial statements are not audited. It shows how the business has moved since the last annual report, and what management says changed.

Sep 30, 2026 · Filed Nov 10, 2026

CRBP$3.93+11.6%Stored close · as of Nov 10, 2026

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Notes to Condensed Consolidated Financial Statements

Notes to Unaudited Condensed Consolidated Financial Statements

September 30, 2026

  1. NATURE OF BUSINESS AND BASIS OF PRESENTATION

Nature of Business

Corbus Pharmaceuticals Holdings, Inc. (the "Company" or "Corbus") is a clinical-stage company focused on developing new therapies in oncology and obesity and is committed to helping people defeat serious illness by bringing innovative scientific approaches to well-understood biological pathways. Corbus’ pipeline includes sutantatug envedotin (CRB-701), a next-generation antibody drug conjugate ("ADC") for the treatment of Nectin-4-expressing tumors and CRB-913, an orally delivered highly peripherally restricted cannabinoid type-1 ("CB1") inverse agonist for the treatment of obesity. Since its inception, the Company has devoted substantially all of its efforts to business planning, research and development, recruiting management and technical staff, acquiring operating assets and raising capital. The Company’s business is subject to significant risks and uncertainties and the Company will be dependent on raising substantial additional capital before it becomes profitable, and it may never achieve profitability.

Basis of Presentation

The accompanying unaudited financial statements have been prepared in accordance with generally accepted accounting principles in the United States ("U.S. GAAP") for interim financial reporting. In the opinion of management of the Company, the accompanying unaudited condensed consolidated interim financial statements reflect all adjustments (which include only normal recurring adjustments) necessary to present fairly, in all material respects, the condensed consolidated financial position of the Company as of September 30, 2026 and the results of its operations and changes in stockholders’ equity for the three and nine months ended September 30, 2026 and 2025 and its cash flows for the nine months ended September 30, 2026 and 2025. Certain amounts in the prior year's financial statements have been reclassified to conform with the current year presentation. These reclassifications did not impact previously reported net loss or cash flows. The December 31, 2025 condensed consolidated balance sheet was derived from audited financial statements. The Company prepared the condensed consolidated financial statements following the requirements of the U.S. Securities and Exchange Commission (the "SEC") for interim reporting. Accordingly, certain information and footnote disclosures normally included in annual financial statements prepared in accordance with U.S. GAAP have been condensed or omitted. It is suggested that these condensed consolidated financial statements be read in conjunction with the financial statements and notes thereto included in the Company’s Annual Report on Form 10-K for the year ended December 31, 2025, filed on March 9, 2026 (the "2025 Annual Report"). The results of operations for such interim periods are not necessarily indicative of the operating results for the full fiscal year.

Basis of Consolidation

The condensed consolidated financial statements include the accounts of the Company and its wholly owned subsidiaries. All significant intercompany transactions and accounts have been eliminated in consolidation.

The significant accounting policies used in preparation of these condensed consolidated financial statements in this Form 10-Q are consistent with those discussed in Note 3, "Significant Accounting Policies," in our 2025 Annual Report.

  1. LIQUIDITY

The accompanying condensed consolidated financial statements have been prepared assuming the Company will continue as a going concern, which contemplates continuity of operations, realization of assets and the satisfaction of liabilities and commitments in the normal course of business. The Company has incurred recurring losses since inception and as of September 30, 2026, had an accumulated deficit of approximately $651.2 million. The Company anticipates operating losses to continue for the foreseeable future due to, among other things, costs related to research funding, development of its product candidates and its pre-clinical and clinical programs, strategic alliances, and the development of its administrative organization. Based on current operating plans and assumptions regarding clinical timelines and other planned expenditures, the Company expects that its cash, cash equivalents, and investments of approximately $115.3 million at September 30, 2026 will be sufficient to meet its operating and capital requirements at least twelve months from the issuance of this Quarterly Report on Form 10-Q.

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The source, timing and availability of any future financing will depend principally upon market conditions, and, more specifically, on the progress of the Company’s clinical development programs. Funding may not be available when needed, at all, or on terms acceptable to the Company. Lack of necessary funds may require the Company to, among other things, delay, scale back or eliminate some or all of the Company’s planned clinical or pre-clinical trials.

The Company filed a new shelf registration statement which was declared effective on March 20, 2026 for which the Company is authorized to offer and sell securities up to $300 million.

  1. CASH, CASH EQUIVALENTS, AND RESTRICTED CASH

The Company considers only those investments which are highly liquid, readily convertible to cash, and that mature within 90 days from the date of purchase to be cash equivalents. At September 30, 2026 and December 31, 2025, cash equivalents were comprised of money market funds and corporate debt securities with maturities less than 90 days from the date of purchase.

Restricted cash as of September 30, 2026 included security for a stand-by letter of credit issued in favor of a landlord for $0.4 million, all of which was classified in noncurrent assets as of September 30, 2026.

Cash, cash equivalents, and restricted cash consist of the following (in thousands):

September 30, 2026 · December 31, 2025
Cash$3,893$1,351
Cash equivalents26,35327,141
Cash and cash equivalents30,24628,492
Restricted cash, current—670
Restricted cash, noncurrent385—
Restricted cash385670
Total cash, cash equivalents, and restricted cash shown in the statement of cash flows$30,631$29,162

As of September 30, 2026, the Company’s cash and cash equivalents held in the U.S. was approximately $26.6 million and approximately $3.6 million of cash was held in its subsidiaries in the U.K. and Australia. As of December 31, 2025, all of the Company’s cash was held in the U.S., except for approximately $1.2 million of cash which was held in its subsidiaries in the U.K. and Australia.

  1. INVESTMENTS

The following table summarizes the Company’s investments as of September 30, 2026 (in thousands):

Amortized Cost · GrossUnrealizedGain · GrossUnrealizedLosses · Fair Value
Debt Securities:
U.S. government agency securities$1,015$-$(17)$998
Commercial paper16,711--16,711
Corporate debt securities67,560-(178)67,382
Total$85,286$—$(195)$85,091

The following table summarizes the amortized cost and fair value of the Company’s available-for-sale marketable debt securities by contractual maturity as of September 30, 2026 (in thousands):

Amortized CostFair Value
Maturing in one year or less$81,258$81,109
Maturing after one year but less than three years4,0283,982
$85,286$85,091

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The following table summarizes the Company’s investments as of December 31, 2025 (in thousands):

Amortized Cost · GrossUnrealizedGain · GrossUnrealizedLosses · Fair Value
Debt Securities:
Commercial paper$33,846$-$-$33,846
Corporate debt securities100,98320(72)100,931
Total$134,829$20$(72)$134,777

The following table summarizes the amortized cost and fair value of the Company’s available-for-sale marketable debt securities by contractual maturity as of December 31, 2025 (in thousands):

Amortized CostFair Value
Maturing in one year or less$123,934$123,903
Maturing after one year but less than three years10,89510,874
$134,829$134,777
  1. FAIR VALUE OF FINANCIAL ASSETS AND LIABILITIES

The following table presents information about the Company’s financial assets and liabilities measured at fair value on a recurring basis and indicates the level of the fair value hierarchy utilized to determine such fair values as of September 30, 2026 (in thousands):

Level 1Level 2Level 3Total
Assets:
Cash equivalents:
Money market funds$24,837$—$—$24,837
Corporate debt securities—1,516—1,516
Investments:
U.S. government agency securities—998—998
Commercial paper—16,711—16,711
Corporate debt securities—67,382—67,382
$24,837$86,607$—$111,444

The following table presents information about the Company’s financial assets and liabilities measured at fair value on a recurring basis and indicates the level of the fair value hierarchy utilized to determine such fair values as of December 31, 2025 (in thousands):

Level 1Level 2Level 3Total
Assets:
Cash equivalents:
Money market funds$23,037$—$—$23,037
Commercial paper—1,488—1,488
Corporate debt securities—2,616—2,616
Investments:
Commercial paper—33,846—33,846
Corporate debt securities—100,931—100,931
$23,037$138,881$—$161,918

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  1. PREPAID EXPENSES AND OTHER CURRENT ASSETS

Prepaid expenses and other current assets consisted of the following (in thousands):

September 30,2026December 31,2025
Prepaid expenses$1,408$1,210
Other current assets2,2061,805
Prepaid expenses and other current assets$3,614$3,015

As of September 30, 2026, other current assets included in the prepaid expenses and other current assets line within the condensed consolidated balance sheet includes $1.5 million related to government tax credits that were recorded during the fourth quarter of 2024 that have not yet been received.

  1. LICENSE AGREEMENTS

The Company entered into a license agreement (the "Jenrin License Agreement") with Jenrin Discovery, LLC ("Jenrin"), a privately held Delaware limited liability company, effective September 20, 2018. Pursuant to the Jenrin License Agreement, Jenrin granted the Company exclusive worldwide rights to develop and commercialize the Licensed Products (as defined in the Jenrin License Agreement) which includes the Jenrin library of over 600 compounds and multiple issued and pending patent filings. The compounds are designed to treat inflammatory and fibrotic diseases by targeting the endocannabinoid system.

Inconsideration of the license and other rights granted by Jenrin, the Company paid Jenrin a $0.3 million upfront cash payment and is obligated to pay Jenrin up to $18.4 million in potential milestone payments for each compound it elects to develop based upon the achievement of specified development and regulatory milestones. In addition, the Company is obligated to pay Jenrin royalties in the mid, single digits based on net sales of any Licensed Products, subject to specified reductions. The Company achieved the first milestone in the amount of$0.4 million associated with the progression into a clinical trial for CRB-913 during the first quarter of 2025, which was subsequently paid in the second quarter of 2025. The Company is obligated to pay Jenrin up to $18.0 million in additional potential milestone payments for further development of CRB-913.

The Company entered into a license agreement (the "UCSF License Agreement") with the Regents of the University of California ("The Regents") effective May 26, 2021. Pursuant to the UCSF License Agreement, the Company received an exclusive license to certain patents relating to humanized antibodies against integrin αvβ8, one of which the Company is referring to as CRB-601, along with non-exclusive licenses to certain related know-how and materials. The Company amended the UCSF License Agreement with The Regents effective November 17, 2022, adding additional antibody patents to the agreement.

Inconsideration for the license and other rights granted to the Company under the UCSF License Agreement, the Company paid The Regents a license issue fee of $1.5 million. In consideration for the additional antibody patents granted to the Company, the Company paid The Regents a license issue fee of $0.8 million, paid in two equal installments of $0.4 million.

The Company further amended the UCSF License Agreement with The Regents effective August 14, 2023 to incorporate certain new technology rights and amend the payment schedule for the development milestone for the filing of patent rights and the development milestone for the filing of an Investigational New Drug ("IND").

In addition to the license issuance fees, the Company is obligated to pay an annual license maintenance fee, as well as up to $150.8 million in remaining potential milestone payments, excluding indication milestones for antibodies used for diagnostic products and services that will be an additional $50.0 thousand for each new indication, for the achievement of certain development, regulatory, and sales milestones. In addition, the Company is also obligated to pay royalties in the lower, single digits on sales of products falling within the scope of the licensed patents, which is subject to a minimum annual royalty obligation, and a percentage share of certain payments received by the Company from sublicensees or in connection with the sale of the licensed program. During the first quarter of 2025, the Company paid $1.6 million under the UCSF License Agreement for previously achieved milestone payments.

The Company entered into a license agreement (the "CSPC License Agreement") with CSPC Megalith Biopharmaceutical Co., Ltd. ("CSPC"), a subsidiary of CSPC Pharmaceutical Group Limited, effective February 12, 2023. Pursuant to the CSPC License Agreement, the Company received an exclusive license to develop and commercialize a novel clinical stage ADC targeting Nectin-4, which the Company is referring to as sutantatug envedotin, in the U.S., Canada, the European Union (including the European Free Trade Area), the U.K., and Australia.

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In consideration for the license granted to the Company under the CSPC License Agreement, the Company paid CSPC an upfront payment of $7.5 million ($5.0 million paid at signing during the first quarter of 2023 followed by $2.5 million paid during the third quarter of 2024). In April 2026, the Company paid CSPC $10.0 million pursuant to the achievement of a development milestone. The Company achieved a second development milestone in the amount of$15.0 million during the third quarterof 2026. This amount is included in accrued expenses within the condensed consolidated balance sheets as of September 30, 2026. In addition to this accrual, the Company is obligated to pay remaining potential milestone payments to CSPC totaling up to $105.0 million based upon the achievement of specified development and regulatory milestones and $555.0 million in potential commercial milestone payments. Furthermore, the Company is obligated to pay royalties in the low double digits based on net sales of any Licensed Products, as defined in the CSPC License Agreement.

The Company determined that substantially all of the fair value of the Jenrin License Agreement, UCSF License Agreement and CSPC License Agreement was attributable to a single or separate groups of in-process research and development assets which did not constitute a business. The Company concluded that it did not have any alternative future use for the acquired in-process research and development assets. Thus, the Company recorded the various upfront payments to research and development expenses in the quarter the license deals became effective. The Company will account for the development, regulatory, and sales milestone payments in the period that the relevant milestones are achieved as either research and development expense or as an intangible asset as applicable. Research and development expenses associated with upfront payments and clinical milestones were $15.0 million and$25.0 million for the three and nine months ended September 30, 2026, respectively, related to the development milestones in accordance with the CSPC License Agreement. Research and development expenses associated with upfront payments and clinical milestones were $0 and $0.4 million for thethree and nine months ended September 30, 2025, respectively, related to the CRB-913 milestone payment in accordance with the Jenrin License Agreement.

  1. PROPERTY AND EQUIPMENT

Property and equipment consisted of the following (in thousands):

September 30,2026December 31,2025
Computer hardware and software$47$20
Office furniture and equipment1,1141,114
Leasehold improvements3,3313,331
Property and equipment, gross4,4924,465
Less: accumulated depreciation(4,456)(4,306)
Property and equipment, net$36$159

Depreciation expense was $0.1 million for each of the three months ended September 30, 2026 and 2025 and $0.2 millionfor each of the nine months ended September 30, 2026 and 2025.

No impairment charges were recognized during thethree and nine months ended September 30, 2026 and 2025.

  1. LEASES

Operating Lease Commitment

In April 2026, the Company entered into the third amendment to its existing lease of office space (the "April 2026 Lease Agreement"). The April 2026 Lease Agreement extends the term of the lease to February 29, 2032, with an option to extend the lease term for an additional period of five years upon notice to the landlord. In addition, the April 2026 Lease Agreement reduces the leased space from 62,756 square feet under the February 2019 Lease Agreement to 36,471 square feet beginning on December 1, 2026 with new monthly base rent of approximately $65.0 thousand per month beginning March 1, 2027, with annual base rent escalation clauses during the lease term. The Company is also obligated to pay to the landlord certain operating costs. The landlord will reimburse the Company for up to $0.2 million of improvements to the leased space. The Company accounted for the lease amendment as a modification of the existing lease and remeasured the right-of-use asset and lease liability, discounted at the Company's estimated incremental borrowing rate of 11%. The incremental borrowing rate is the rate of interest that the Company would have to pay to borrow, on a collateralized basis, an amount equal to the lease payments over a similar term equal to the lease term in a similar economic environment. As of September 30, 2026, the weighted-average remaining lease term was approximately 5.4 years. Cash paid for rent expense recorded during thethree and nine months ended September 30, 2026 was $0.5 million and $1.4 million, respectively.

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Pursuant to the terms of the Company’s non-cancelable lease agreements in effect at September 30, 2026, the following table summarizes the Company’s maturities of operating lease liabilities as of September 30, 2026 (in thousands):

2026$309
2027653
2028953
20291,018
20301,054
Thereafter1,273
Total lease payments5,260
Less: imputed interest(1,351)
Total$3,909
  1. ACCRUED EXPENSES

Accrued expenses consisted of the following (in thousands):

September 30,2026December 31,2025
Accrued pre-clinical and clinical costs$10,514$12,211
Accrued product development costs1,3001,454
Accrued license costs15,000—
Accrued compensation2,6562,859
Accrued administrative costs697320
Total$30,167$16,844
  1. NET LOSS PER COMMON SHARE

Basic and diluted net loss per share of the Company’s common stock has been computed by dividing net loss by the weighted average number of shares outstanding during the period. For periods in which there is a net loss, options, warrants and RSUs are anti-dilutive and therefore excluded from diluted loss per share calculations. The following table sets forth the computation of basic and diluted earnings per share for thethree and nine months ended September 30, 2026 and 2025 (in thousands except share and per share amounts):

Three Months EndedSeptember 30,Nine Months EndedSeptember 30,
2026202520262025
Net loss$(37,754)$(23,342)$(95,760)$(57,982)
Weighted average number of common shares-basic and diluted20,837,78712,307,29819,658,50612,250,315
Net loss per share of common stock-basic and diluted$(1.81)$(1.90)$(4.87)$(4.73)

The 1,025,000 pre-funded warrants issued in November 2025 and outstanding as of September 30, 2026 (see Note 12) were included in computing the weighted average common shares outstanding used in calculating basic and diluted net loss per share.

The following common stock equivalents have been excluded from the calculation of diluted net loss per share for the periods presented because including them would have been anti-dilutive:

September 30,
20262025
Stock options2,168,2661,436,569
Unvested restricted stock units690,745496,405
Warrants2,8732,873

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  1. STOCKHOLDERS' EQUITY

Preferred Stock

The Company has authorized 10,000,000 shares of preferred stock, $0.0001 par value per share, of which 0 shares were issued and outstanding as of September 30, 2026 and December 31, 2025, respectively.

Common Stock

The Company has authorized 300,000,000 shares of common stock, $0.0001 par value per share, of which 20,606,760 and 17,611,511 shares were issued and outstanding as of September 30, 2026 and December 31, 2025, respectively.

2025 Public Offering

On October 30, 2025, the Company entered into an underwriting agreement with Jefferies LLC ("Jefferies"), as representative of the several underwriters, relating to an underwritten public offering of 4,744,231 shares of common stock at a price to the public of $13.00 per share, and, to certain investors in lieu of common stock, pre-funded warrants to purchase 1,025,000 shares of common stock at a public offering price of $12.9999 per pre-funded warrant. The purchase price per share of each pre-funded warrant represents the per share public offering price for the common stock, minus the $0.0001 per share exercise price of each such pre-funded warrant. On November 3, 2025, the Company completed the public offering raising gross proceeds of $75.0 million and net proceeds of $70.2 million after deducting underwriting discounts and commissions and other offering expenses payable by the Company. The pre-funded warrants were classified as a component of permanent equity on the balance sheet as they are freestanding financial instruments that are immediately exercisable and permit the holders to receive a fixed number of shares of common stock upon exercise. As of September 30, 2026, all of the pre-funded warrants from the offering remain available for exercise.

Open Market Sale Agreement

On May 31, 2023, the Company entered into Amendment No. 1 to the Open Market Sale Agreement originally dated August 6, 2020 (as amended, the “Open Market Sale Agreement”) with Jefferies as sales agent. Under the Open Market Sale Agreement, the Company may issue and sell, from time to time through Jefferies, shares of its common stock having an aggregate offering price of up to $150.0 million (the “Open Market Offering”). On August 7, 2026, the Company filed a new prospectus supplement pursuant to its existing shelf registration, providing for the offer and sale of shares of its common stock having an aggregate offering price of up to $127.5 million from time to time through Jefferies pursuant to the Open Market Sale Agreement. The $127.5 million offering amount represents the new aggregate offering amount available as of August 7, 2026, prior to any subsequent sales.

Under the Open Market Sale Agreement, Jefferies may sell the common stock by any method permitted by law deemed to be an “at-the-market offering” as defined by Rule 415(a)(4) promulgated under the Securities Act of 1933, as amended. The Company may sell common stock in amounts and at times to be determined by the Company subject to the terms and conditions of the Open Market Sale Agreement, but the Company has no obligation to sell any of the common stock in the Open Market Offering.

The Company has agreed to pay Jefferies a commission of 3.0% of the aggregate gross proceeds from each sale of common stock and have agreed to provide Jefferies with customary indemnification and contribution rights. The Company has also agreed to reimburse Jefferies for certain specified expenses.

During the three and nine months ended September 30, 2026, the Company sold 1,932,621 and 2,826,665 shares of its common stock, respectively, pursuant to the Open Market Sale Agreement for which the Company received net proceeds of approximately$18.6 million and $27.6 million, respectively. During the three and nine months ended September 30, 2025, the Company sold 272,938 shares of its common stock, pursuant to the Open Market Sale Agreement for which the Company received net proceeds of approximately $2.9 million. As of September 30, 2026, approximately$115.2 million was available for issuance and sale under the Open Market Offering and the Company may increase the dollar amount of common stock available for issuance and sale under the Open Market Sale Agreement at any time by filing a new or additional prospectus supplement.

Other Common Stock Transactions

During the three and nine months ended September 30, 2026, the Company issued 2,641 and 167,772 common shares from the vesting of shares from restricted stock units ("RSUs"), respectively. During the three and nine months ended September 30, 2025, the Company issued 7,846 and 82,433 common shares from the vesting of shares from RSUs, respectively.

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  1. STOCK-BASED COMPENSATION AWARDS

On May 16, 2024, the Company's stockholders approved the 2024 Equity Compensation Plan (the "2024 Plan") authorizing the issuance of up to 2,000,000 shares, succeeding the 2014 Equity Compensation Plan (the "2014 Plan"), under which no further grants may be made pursuant to the terms of the 2014 Plan. On May 13, 2026, in connection with the Company's annual stockholders meeting, stockholders approved an amendment to the 2024 Plan to increase the number of shares of common stock authorized for issuance thereunder by 3,000,000 shares to 5,000,000 shares. Pursuant to the 2024 Plan, theboard of directors ("Board") may grant nonqualified stock options, incentive stock options, stock appreciation rights, restricted stock, RSUs, performance shares, performance units, incentive bonus awards, other cash-based awards and other stock-based awards to employees, officers, non-employee directors, and other individual service providers.

Under the terms of the 2024 Plan and 2014 Plan, the Company granted stock options and RSUs to employees, officers, non-employee directors, consultants and advisors. Stock options have a ten-year term and an exercise price equal to the fair market value of a share of our common stock on the grant date. Stock options generally vest over four years with 25% vesting on the one-year anniversary of the grant date and the remainder vesting in equal monthly installments thereafter, except for grants to non-employee directors that vest annually. RSUs generally vest over a period of one to four years in annual installments beginning on the first anniversary of the grant date.

On June 17, 2026, the Board adopted the 2026 Inducement Award Plan (the "2026 Inducement Plan"). Under the 2026 Inducement Plan, the Company may, at its discretion, grant awards to any employee who is eligible to receive an employment inducement grant pursuant to the “inducement” grant exception under Rule 5635(c)(4) of the Marketplace Rules of the Nasdaq Stock Market LLC. The Company has initially reserved 1,000,000 shares of its common stock for the issuance of awards under the 2026 Inducement Plan.

As of September 30, 2026, an aggregateof 632,364 shares of common stock were reserved for issuance upon the exercise or vesting of outstanding awards under the 2014 Plan. No additional grants can be made under the 2014 Plan.

As of September 30, 2026, an aggregate of 1,976,638 shares of common stock were reserved for issuance upon the exercise or vesting of outstanding awards and up to 2,881,332 shares of common stock may be issued pursuant to awards granted under the 2024 Plan.

As of September 30, 2026, an aggregate of 250,009 shares of common stock were reserved for issuance upon the exercise or vesting of outstanding awards and up to 749,991 shares of common stock may be issued pursuant to awards granted under the 2026 Inducement Plan.

Stock-based Compensation Expense

Inconnection with all stock-based compensation awards, total non-cash, stock-based compensation expense recognized in the condensed consolidated statements of operations and comprehensive loss was as follows (in thousands):

Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Research and development expenses$481$509$1,657$1,451
General and administrative expenses1,3271,0733,8733,408
Total stock-based compensation$1,808$1,582$5,530$4,859

The total stock-based compensation expense recognized by award type was as follows (in thousands):

Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Stock options$1,118$948$3,418$2,853
Restricted stock units6906342,1122,006
Total stock-based compensation$1,808$1,582$5,530$4,859

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Stock Options

The fair value of each stock option award is estimated on the date of grant using the Black-Scholes stock option pricing model that uses the assumptions noted in the following table, except for the expected term for non-employees as noted in the following paragraph. The expected term of employee and non-employee director stock options granted under the 2014 Plan and 2024 Plan, all of which qualify as "plain vanilla" per SEC Staff Accounting Bulletin 107, is determined based on the simplified method due to the Company’s limited operating history. The expected term is applied to the stock option grant group as a whole, as the Company does not expect substantially different exercise or post-vesting termination behavior among our employee population. For non-employee stock options, excluding directors, the Company has elected to utilize the contractual term as the expected term. The risk-free rate is based on the yield of a U.S. Treasury security with a term consistent with that used to value the stock option. The Company accounts for forfeitures as they occur.

The weighted average assumptions used principally in determining the fair value of stock options granted to employees andnon-employee directors were as follows:

Nine Months Ended September 30,
20262025
Risk-free interest rate4.11%4.35%
Expected dividend yield0%0%
Expected term in years6.196.15
Expected volatility132.01%131.47%

A summary of stock option activity for thenine months ended September 30, 2026 is presented below:

Stock Options · Shares · Weighted AverageExercise Price · Weighted Average Remaining Contractual Term in Years · AggregateIntrinsic Value (in thousands)
Outstanding at December 31, 20251,386,020$37.407.41$371
Granted1,061,6639.59
Exercised(812)9.79
Forfeited or canceled(191,886)11.35
Expired(86,719)26.69
Outstanding at September 30, 20262,168,266$26.527.88$203
Exercisable at September 30, 2026838,540$52.135.88$150

The weighted average grant-date fair value of stock options granted during the nine months ended September 30, 2026 and 2025 was $8.74 and $8.47 per share, respectively. The aggregate intrinsic value of stock options exercised during the nine months ended September 30, 2026 was $1 thousand. No stock options were exercised during thenine months ended September 30, 2025. As of September 30, 2026, there was $11.4 million of total unrecognized compensation expense related to unvested stock-based option compensation arrangements, which are expected to be recognized over a weighted average period of 1.54 years.

Restricted Stock Units

A RSU represents the right to receive one share of our common stock upon vesting of the RSU. The fair value of each RSU is based on the closing price of our common stock on the date of grant. The Company accounts for forfeitures as they occur.

A summary of RSU activity for the nine months ended September 30, 2026 is presented below:

RSUsNumber of Shares Underlying RSUsWeighted AverageGrant Date Fair Value
Unvested at December 31, 2025498,543$14.78
Granted453,795$9.77
Forfeited(93,821)$13.91
Vested(167,772)$14.76
Unvested at September 30, 2026690,745$11.61

-16-

As of September 30, 2026, there was $6.5 million of unrecognized compensation expense related to unvested RSUs, which are expected to be recognized over a weighted average period of 1.81 years.

  1. WARRANTS

No warrants were exercised during thethree and nine months ended September 30, 2026 and 2025.

On July 28, 2020, the Company entered into the Loan and Security Agreement with K2HV and in connection with the funding of $20.0 million, the Company issued a warrant exercisable for 2,873 shares of the Company’s common stock (the "K2 Warrant") at an exercise price of $208.80 per share. The K2 Warrant is immediately exercisable for 2,873 shares and expires on July 28, 2030. These warrants remain outstanding at September 30, 2026.

The Company also has pre-funded warrants to purchase 1,025,000 shares of common stock at an exercise price of $0.0001 per share with no expiration date that were issued in the 2025 public offering.

  1. SEGMENT INFORMATION

Operating segments are defined as components of an enterprise for which separate discrete information is available for evaluation by the chief operating decision maker in deciding how to allocate resources in assessing performance. The Company views its operations and manages its business inone reportable segment, which is developing and commercializing therapeutics for cancer and obesity. The Company's Chief Executive Officer is the Chief Operating Decision Maker ("CODM").

The accounting policies of the single segment are the same as those described in the summary of significant accounting policies. The CODM assesses performance for the segment based on net income (loss), which is reported on the Company's condensed consolidated statements of operations and comprehensive loss. The measure of segment assets is reported on the condensed consolidated balance sheets as total consolidated assets. All material long-lived assets are located in the United States. Long-lived assets consist of property and equipment, net, and operating lease right-of-use assets.

To date, the Company has not generated any product revenue. The Company expects to continue to incur significant expenses and operating losses for the foreseeable future as it advances product candidates through all stages of development and clinical trials and, ultimately, seek regulatory approval.

As such, the CODM uses cash forecast models in deciding how to allocate resources. Such cash forecast models are reviewed to assess the entity-wide operating results and performance. Net loss is reviewed against budgeted expectations to assess performance of the segment.

The table below summarizes the significant expense categories regularly provided to the CODM for the three and nine months ended September 30, 2026 and 2025 (in thousands):

Three Months Ended September 30, · For the Nine Months Ended September 30,
2026 · 2025 · 2026 · 2025
Operating Expenses:
Research and development
Sutantatug envedotin$26,820$9,579$54,991$21,885
CRB-9134,2663,66618,49710,207
CRB-601994,8052,28611,431
Other drug development121128342374
Total program specific costs31,30618,17876,11643,897
Unallocated internal costs:
Personnel related2,4812,3137,6416,571
Other unallocated4603691,4841,221
Total research and development expenses$34,247$20,860$85,241$51,689
General and administrative4,5773,55714,07711,655
Other income, net1,0701,0753,5585,362
Net Loss$(37,754)$(23,342)$(95,760)$(57,982)

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