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Corbus Pharmaceuticals Reports Q2 2026 Financial Results and Provides a Corporate Update

(Moderate)
(Very Positive)
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Corbus Pharmaceuticals (NASDAQ: CRBP) reported Q2 2026 net loss of approximately $35.0 million, or $1.81 per share, versus $17.7 million, or $1.44 per share, a year earlier. Operating expenses rose to about $36.2 million from $19.2 million, mainly due to higher clinical costs including a $10.0 million milestone payment under the CRB-701 license.

Corbus obtained FDA clearance for TEMPO-1, a Phase 3 registrational study (n=250) of CRB-701 in second-line oropharyngeal squamous cell carcinoma, with enrollment expected to start in September 2026. The company completed last patient last visit in the 240-patient CANYON-1 Phase 1b obesity study of CRB-913 and plans topline data in September 2026. Leadership was strengthened with a new Chief Medical Officer, Chief Business Officer, and Board member. Corbus held $117.9 million in cash, cash equivalents, and investments as of June 30, 2026, which it expects to fund operations into 2028.

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Positive

  • FDA clearance for TEMPO-1 Phase 3 registrational study of CRB-701 in 2L OPSCC (n=250), enrollment expected September 2026
  • Completed last patient last visit in 240-patient CANYON-1 Phase 1b obesity study of CRB-913; topline data planned September 2026
  • CRB-701 holds Fast Track designations from FDA for Nectin-4–expressing oropharyngeal and cervical cancers
  • Cash, cash equivalents, and investments of $117.9 million at June 30, 2026, expected by the company to fund operations into 2028
  • Strengthened leadership with new Chief Medical Officer, Chief Business Officer, and Board member to support registrational studies and commercialization readiness

Negative

  • Q2 2026 net loss widened to approximately $35.0 million from $17.7 million year over year
  • Q2 2026 operating expenses increased to about $36.2 million from $19.2 million, including a $10.0 million CRB-701 milestone payment
  • First half 2026 net loss rose to approximately $58.0 million from $34.6 million in the prior-year period
  • Total stockholders’ equity declined to $102.2 million at June 30, 2026, from $147.5 million at December 31, 2025

News Explained

At June 30, Corbus reported $23,370 thousand in cash, $94,571 thousand in investments, and 18,671,498 common shares outstanding.

The company’s August 6, 2026 Q2 report is a completed financial disclosure; its June 30, 2026 balance sheet separates reported liquidity into $23,370 thousand of cash and $94,571 thousand of investments, alongside the company’s existing common-share base.

Common shares outstanding were 18,671,498 at June 30, 2026, compared with 17,611,511 at December 31, 2025; the release reports the changed share count without specifying a transaction mechanism.

Market Context

The active S-3 shelf, dated March 11, 2026, provides context for this cash-funded development update...
Analysis

The active S-3 shelf, dated March 11, 2026, provides context for this cash-funded development update. Insider records showed Net Buying, while current short positioning was moderate; September enrollment and data reporting remain the stated milestones.

Key Figures

TEMPO-1 enrollment: 250 patients CANYON-1 sample size: 240 patients Net loss: $35.0 million +5 more
8 metrics
TEMPO-1 enrollment 250 patients Registrational study of CRB-701 in 2L OPSCC
CANYON-1 sample size 240 patients Phase 1b study of CRB-913 in obesity
Net loss $35.0 million Three months ended June 30, 2026, versus $17.7 million in 2025
Net loss per share $1.81 Basic and diluted, three months ended June 30, 2026
Operating expenses $36.2 million Three months ended June 30, 2026, versus $19.2 million in 2025
Development milestone payment $10.0 million CRB-701 licensing agreement
Cash and investments $117.9 million On hand as of June 30, 2026
Funding runway Into 2028 Based on current operating plans and planned expenditures

Previous Earnings Reports

5 past events · Latest: May 12 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 12 Q1 earnings report Positive +3.5% Pipeline progress and cash runway accompanied quarterly financial results.
Mar 09 Q4 earnings report Positive +19.2% Clinical updates and completed public offering accompanied full-year financial results.
Nov 12 Q3 earnings report Positive +7.4% Clinical data and financing proceeds accompanied quarterly financial results.
Aug 05 Q2 earnings report Negative -4.7% Quarterly loss and pipeline spending accompanied delayed clinical milestones.
May 06 Q1 earnings report Negative -15.8% Higher quarterly loss accompanied ongoing development of three clinical programs.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Tag-specific earnings events aligned with the announcement sentiment in all five prior observations, with positive earnings events followed by gains and negative events followed by declines.

Key Terms

fast track, antibody drug conjugate, inverse agonist, registrational study
4 terms
fast track regulatory
"The U.S. Food and Drug Administration (FDA) has granted Fast Track designations"
A fast track designation is a regulatory label that speeds up the review and communication between a drug developer and regulators for treatments addressing serious illnesses or unmet medical needs. For investors, it matters because it can shorten development time and reduce regulatory delays—like getting a VIP lane at the airport—raising the chance of earlier market access and potential revenue, though it does not guarantee approval.
antibody drug conjugate technical
"CRB-701 is a next-generation, highly stable Nectin-4 targeting antibody drug conjugate"
An antibody drug conjugate is a targeted medical treatment that combines a special antibody with a powerful drug, allowing precise delivery of the medicine directly to cancer cells or other harmful cells in the body. For investors, it represents a sophisticated approach to therapy that could improve treatment effectiveness and reduce side effects, potentially leading to significant growth opportunities in the biotech and pharmaceutical sectors.
inverse agonist medical
"CRB-913 is a highly peripherally restricted oral CB1 inverse agonist"
An inverse agonist is a type of drug that binds to a biological receptor and reduces the receptor’s natural, ongoing activity, producing the opposite effect of what an activating drug would do. For investors, this matters because inverse agonists can treat conditions where reducing baseline receptor activity is beneficial, potentially creating distinct clinical uses, regulatory pathways, and market value compared with drugs that merely block or activate the same target; think of it as a brake that not only stops a moving car but pushes it slightly backward.
registrational study regulatory
"Obtained FDA clearance to proceed with TEMPO-1 registrational study"
A registrational study is a late-stage clinical trial designed to give the government regulators the evidence they need to decide whether a drug, therapy, or medical device can be approved for sale. Think of it as the final exam or road test for a medical product: its results largely determine whether the product can reach the market, which directly affects potential revenue, company valuation, and investor risk.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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  • Obtained FDA clearance to proceed with registrational study (TEMPO-1) of CRB-701 in 2L oropharyngeal cancer and expect to initiate enrollment in September 2026
  • Concluded last patient last visit in CANYON-1 Phase 1b study (n=240) of CRB-913 in obesity and on track to report data in September 2026
  • Appointed new Chief Medical Officer, Chief Business Officer, and Board Member to strengthen senior leadership and guide the Company through registrational studies and commercialization readiness

NORWOOD, Mass., Aug. 06, 2026 (GLOBE NEWSWIRE) -- Corbus Pharmaceuticals Holdings, Inc. (NASDAQ: CRBP) (“Corbus” or the “Company”), a clinical-stage company focused on developing new therapies in oncology and obesity, today provided a corporate update and reported financial results for the 2026 second quarter ended June 30, 2026. 

"We’ve continued to build momentum as we prepare for two potentially impactful clinical development milestones in September: commencing enrollment of TEMPO-1, our Phase 3 study of CRB-701 in oropharyngeal cancer, and the data readout of CANYON-1, our Phase 1b study of CRB-913 in obesity. Both programs represent opportunities to address areas of significant unmet medical need,” said Yuval Cohen, Ph.D., Chief Executive Officer of Corbus. “CRB-701 has the potential to bring a much-needed therapeutic option for the growing oropharyngeal cancer patient population, for whom approved and other investigational therapies have shown little promise. CRB-913 is a unique daily oral obesity drug candidate with a mechanism of action entirely orthogonal to the GLP-1 class and with the potential for both weight loss and long-term weight management. We look forward to a productive second half of 2026 as we work to improve patient outcomes and generate meaningful value for shareholders.”

Key Corporate and Program Updates 

CRB-701 is a next-generation, highly stable Nectin-4 targeting antibody drug conjugate (ADC) being developed to treat oropharyngeal squamous cell carcinoma (OPSCC), a type of head and neck squamous cell carcinoma (HNSCC), as well as cervical cancer. The U.S. Food and Drug Administration (FDA) has granted Fast Track designations to CRB-701 for the treatment of both cancer types. CRB-701 is licensed from CSPC Megalith Biopharmaceutical Co. Ltd. China.

  • Obtained FDA clearance to proceed with TEMPO-1 registrational study (n=250) of CRB-701 in 2L OPSCC, representing the first registrational trial specifically designed to evaluate a targeted treatment in this patient population.
  • Expect to commence enrollment in the TEMPO-1 study in September 2026.
  • Reported 2L+ monotherapy data from the Phase 1/2 study of CRB-701 in HNSCC and cervical cancers at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting. Link here for press release with more details.
  • Anticipate reporting CRB-701 + Keytruda® combination data in first-line (1L) settings in OPSCC patients in Q1 2027 to support potential further registration-enabling trials in the front line.

CRB-913 is a highly peripherally restricted oral CB1 inverse agonist for the treatment of obesity.

  • Concluded last patient last visit in the CANYON-1 Phase 1b clinical trial of CRB-913 for the treatment of obesity. The CANYON-1 study followed 240 patients over a 12-week treatment period followed by a 4-week safety follow-up.
  • On track to report topline data from CANYON-1 Phase 1b study in September 2026. 

Corporate Appointments

Corbus strengthened its leadership team and Board of Directors with several key appointments in the second quarter of 2026.

  • Leonardo Viana Nicacio, M.D. as Chief Medical Officer. Dr. Nicacio previously served as Chief Medical Officer at Protara Therapeutics and Senior Vice President, Head of Clinical Development and Global Medical Affairs at Stemline Therapeutics. He also held roles of increasing responsibility at Seagen (acquired by Pfizer), most recently as Vice President of Clinical Development, overseeing programs across a range of cancers, including bladder, breast, gynecologic, lung, colorectal, and head and neck cancers, and most notably the development of a therapeutic for metastatic cervical cancer, TIVDAK®.
  • Nishant Saxena as Chief Business Officer. Mr. Saxena most recently served as Chief Financial Officer at Jeune Aesthetics, Inc., a wholly owned subsidiary of Krystal Biotech, Inc. Previously, he served as a Managing Director in Evercore’s healthcare group, where he advised on transactions totaling over $500 billion in aggregate value. Earlier in his career, Mr. Saxena held positions of increasing responsibility in private equity, venture capital, and investment advisory firms.
  • Brent Pfeiffenberger to Board of Directors. Dr. Pfeiffenberger is currently President and Chief Executive Officer of Century Therapeutics and the Chair of its Board of Directors. Previously, Dr. Pfeiffenberger served as Chief Operating Officer of Neogene Therapeutics (acquired by AstraZeneca). Prior to Neogene, he spent nearly two decades in leadership roles of increasing responsibility at Bristol Myers Squibb, most recently as Senior Vice President, Head of U.S. Oncology, where he oversaw business operations for the multi-billion-dollar franchise.

Financial Results for the Quarter Ended June 30, 2026 

The Company reported a net loss of approximately $35.0 million, or a net loss per basic and diluted share of $1.81, for the three months ended June 30, 2026, compared to a net loss of approximately $17.7 million, or a net loss per basic and diluted share of $1.44, for the three months ended June 30, 2025.

Operating expenses increased by $17.0 million to approximately $36.2 million for the three months ended June 30, 2026, compared to approximately $19.2 million for the three months ended June 30, 2025. The increase was primarily attributable to an increase in clinical development expenses, which includes a $10.0 million development milestone payment pursuant to the licensing agreement for CRB-701.

The Company had $117.9 million of cash, cash equivalents, and investments on hand as of June 30, 2026, which is expected to fund operations into 2028 based on current operating plans and planned expenditures.

About Corbus 

Corbus Pharmaceuticals Holdings, Inc. 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 CRB-701, a next-generation antibody drug conjugate for the treatment of Nectin-4-expressing tumors and CRB-913, an orally delivered highly peripherally restricted CB1 inverse agonist for the treatment of obesity. Corbus is headquartered in Norwood, Massachusetts. For more information on Corbus, visit corbuspharma.com. Connect with us on X, LinkedIn and Facebook

Forward-Looking Statements  

This press release contains certain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934 and Private Securities Litigation Reform Act of 1995, as amended, including those relating to the Company’s trial results, product development, clinical and regulatory timelines, including timing for completion of trials and presentation of data, anticipated regulatory interactions and outcomes, including alignment with FDA on trial design, potential accelerated approval market opportunity, competitive position, possible or assumed future results of operations, business strategies, potential growth opportunities, sufficiency of cash runway and other statement that are predictive in nature. These forward-looking statements are based on current expectations, estimates, forecasts and projections about the industry and markets in which we operate and management’s current beliefs and assumptions. 

These statements may be identified by the use of forward-looking expressions, including, but not limited to, “expect,” “anticipate,” “intend,” “plan,” “believe,” “estimate,” “potential,” “predict,” “project,” “should,” “would” and similar expressions and the negatives of those terms. These statements relate to future events or our financial performance and involve known and unknown risks, uncertainties, and other factors on our operations, clinical development plans and timelines, which may cause actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Such factors include those set forth in the Company’s filings with the Securities and Exchange Commission including those described in our Annual Report on Form 10-K for the year ended December 31, 2025, and other filings we make with the Securities and Exchange Commission. Prospective investors are cautioned not to place undue reliance on such forward-looking statements, which speak only as of the date of this press release. The Company undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise, except as required by law. 

All product names, logos, brands and company names are trademarks or registered trademarks of their respective owners.  Their use does not imply affiliation or endorsement by these companies.  

INVESTOR CONTACTS:  
Sean Moran 
Chief Financial Officer 
Corbus Pharmaceuticals 
smoran@corbuspharma.com 

Dan Ferry 
Managing Director 
LifeSci Advisors, LLC 
daniel@lifesciadvisors.com 

MEDIA CONTACT:
Liz Melone
Founder & Principal
Melone Communications, LLC
liz@melonecomm.com

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Corbus Pharmaceuticals Holdings, Inc.
Condensed Consolidated Statements of Operations and Comprehensive Loss
(in thousands, except share and per share amounts)
(Unaudited)
       
  For the Three Months
Ended June 30,
  For the Six Months Ended
June 30,
 
  2026  2025  2026  2025 
Operating expenses:            
Research and development $31,175  $15,187  $50,994  $30,829 
General and administrative  5,015   3,965   9,500   8,098 
Total operating expenses  36,190   19,152   60,494   38,927 
Operating loss  (36,190)  (19,152)  (60,494)  (38,927)
Other income (expense), net:            
Interest and investment income, net  1,164   1,314   2,566   2,995 
Other (expense) income, net  (11)  176   (78)  1,292 
Total other income, net  1,153   1,490   2,488   4,287 
Net loss $(35,037) $(17,662) $(58,006) $(34,640)
Net loss per share, basic and diluted $(1.81) $(1.44) $(3.04) $(2.83)
Weighted average number of common shares outstanding, basic and diluted  19,407,688   12,240,443   19,059,092   12,221,373 
             
Comprehensive loss:            
Net loss $(35,037) $(17,662) $(58,006) $(34,640)
Other comprehensive loss:            
Change in unrealized gain (loss) on marketable debt securities  54   (16)  (54)  (74)
Total other comprehensive income (loss)  54   (16)  (54)  (74)
Total comprehensive loss $(34,983) $(17,678) $(58,060) $(34,714)
                 


Corbus Pharmaceuticals Holdings, Inc.
Condensed Consolidated Balance Sheets
(in thousands, except share and per share amounts)
       
  June 30, 2026
(unaudited)
  December 31, 2025 
       
ASSETS      
Current assets:      
Cash and cash equivalents $23,370  $28,492 
Investments  94,571   134,777 
Restricted cash     670 
Prepaid expenses and other current assets  4,812   3,015 
Total current assets  122,753   166,954 
Restricted cash  385    
Property and equipment, net  71   159 
Operating lease right-of-use assets  3,779   1,082 
Total assets $126,988  $168,195 
LIABILITIES AND STOCKHOLDERS’ EQUITY      
Current liabilities:      
Accounts payable $5,254  $2,215 
Accrued expenses  15,230   16,844 
Operating lease liabilities  999   1,633 
Total current liabilities  21,483   20,692 
Operating lease liabilities, noncurrent  3,265    
Total liabilities  24,748   20,692 
Stockholders’ equity:      
Preferred stock, $0.0001 par value; 10,000,000 shares authorized, no shares issued and outstanding at June 30, 2026 and December 31, 2025      
Common stock, $0.0001 par value; 300,000,000 shares authorized,
18,671,498 and 17,611,511 shares issued and outstanding at June 30, 2026 and December 31, 2025, respectively
  2   2 
Additional paid-in capital  715,781   702,984 
Accumulated deficit  (613,436)  (555,430)
Accumulated other comprehensive loss  (107)  (53)
Total stockholders’ equity  102,240   147,503 
Total liabilities and stockholders’ equity $126,988  $168,195 



FAQ

What were Corbus Pharmaceuticals (CRBP) Q2 2026 financial results?

Corbus reported a Q2 2026 net loss of about $35.0 million, or $1.81 per share. According to Corbus, operating expenses increased to roughly $36.2 million, driven mainly by higher clinical development costs, including a $10.0 million milestone payment related to the CRB-701 licensing agreement.

What does FDA clearance of the TEMPO-1 trial mean for Corbus Pharmaceuticals (CRBP)?

FDA clearance allows Corbus to proceed with TEMPO-1, a Phase 3 registrational study of CRB-701 in second-line oropharyngeal squamous cell carcinoma. According to Corbus, this 250-patient trial is the first registrational study specifically designed for targeted treatment in this population, with enrollment expected September 2026.

When will Corbus Pharmaceuticals (CRBP) report CANYON-1 Phase 1b obesity data for CRB-913?

Corbus plans to report topline data from the CANYON-1 Phase 1b obesity trial of CRB-913 in September 2026. According to Corbus, the 12-week study followed 240 patients, with an additional four-week safety follow-up, and last patient last visit has already been completed.

How much cash does Corbus Pharmaceuticals (CRBP) have and what is the runway?

Corbus had $117.9 million in cash, cash equivalents, and investments as of June 30, 2026. According to Corbus, this balance, together with current operating plans and planned expenditures, is expected to fund operations into 2028, supporting ongoing and planned clinical programs.

What leadership changes did Corbus Pharmaceuticals (CRBP) announce in Q2 2026?

Corbus appointed Leonardo Viana Nicacio, M.D. as Chief Medical Officer, Nishant Saxena as Chief Business Officer, and added Brent Pfeiffenberger to its Board. According to Corbus, these hires are intended to strengthen clinical, business, and commercialization expertise as programs advance to registrational stages.

What are the key clinical programs CRB-701 and CRB-913 at Corbus Pharmaceuticals (CRBP)?

CRB-701 is a Nectin-4–targeting antibody-drug conjugate for oropharyngeal and cervical cancers, holding FDA Fast Track designations. According to Corbus, CRB-913 is an oral, highly peripherally restricted CB1 inverse agonist in development for obesity, currently supported by the CANYON-1 Phase 1b trial.