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Corbus Pharmaceuticals to Host In-Person and Virtual KOL Event at ASCO 2026

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Corbus Pharmaceuticals (NASDAQ: CRBP) will host an in-person and virtual KOL event at ASCO 2026 to present updated Phase 1/2 data for CRB-701 in head and neck squamous cell carcinoma (HNSCC).

The event is June 1, 2026 at Marriott Marquis Chicago; poster data at ASCO May 29–June 2 will include response durability and subgroup analyses from 75 HNSCC participants. The ongoing three-part study has evaluated CRB-701 in 317 advanced solid tumor participants. According to Corbus, the company recently announced broad alignment with the FDA on a registration path for CRB-701 in HNSCC.

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Positive

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Negative

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News Market Reaction – CRBP

+1.43%
+1.43% Session close to close

In the May 5 session, CRBP gained 1.43%, reflecting a mild positive market reaction.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement highlights an upcoming ASCO 2026 KOL event featuring updated Phase 1/2 CRB‑701 dat...
Analysis

This announcement highlights an upcoming ASCO 2026 KOL event featuring updated Phase 1/2 CRB‑701 data in HNSCC, including durability and subgroup analyses from 75 patients within a broader 317-participant trial. It follows prior ASCO‑related disclosures and FDA alignment on CRB‑701’s registrational path, reinforcing the program’s central role. Key factors to watch include the depth of responses, safety signals, and how these data complement earlier CRB‑701 updates discussed in March and April 2026.

Key Figures

HNSCC cohort size: 75 participants Overall trial size: 317 participants ASCO 2026 dates: May 29 – June 2, 2026 +2 more
5 metrics
HNSCC cohort size 75 participants Phase 1/2 CRB-701 monotherapy HNSCC data at ASCO 2026
Overall trial size 317 participants Three-part Phase 1/2 CRB-701 study in advanced solid tumors
ASCO 2026 dates May 29 – June 2, 2026 American Society of Clinical Oncology annual meeting
KOL event time 6:30 AM CT KOL event at Marriott Marquis Chicago on June 1, 2026
Drug-antibody ratio 2 Homogenous drug antibody ratio for CRB-701 ADC

Historical Context

5 past events · Latest: Apr 22 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Apr 22 ASCO data preview Positive +2.8% ASCO 2026 abstracts for updated Phase 1/2 CRB-701 clinical data.
Apr 14 Obesity trial update Positive -1.6% Last Patient First Visit in CANYON-1 Phase 1b obesity study CRB-913.
Apr 07 FDA path alignment Positive -4.2% Broad FDA alignment on CRB-701 registrational study designs in HNSCC and cervical.
Mar 18 Conference participation Neutral -6.0% CEO participation in BMO 2026 Metabolic Health Summit panel on pipeline.
Mar 09 Earnings & update Positive +19.2% Q4 and 2025 results with strong CRB-701/CRB-913 data and cash position.

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

Pattern Detected

CRBP has often reacted positively to stronger data/financial updates, while some clinically positive or event-driven headlines have seen negative or muted price reactions.

Recent Company History

Over the last few months, Corbus has highlighted progress across oncology and obesity. A Q4 and 2025 update on Mar 9, 2026 with encouraging CRB‑701 and CRB‑913 data and strengthened finances coincided with a 19.23% gain. FDA alignment on CRB‑701 registrational paths on Apr 7 saw a -4.24% move despite seemingly positive content. ASCO‑related CRB‑701 data announcements on Apr 22 and obesity trial milestones on Apr 14 produced mixed reactions. Today’s ASCO KOL-event news fits into this ongoing data‑driven narrative for CRB‑701.

Key Terms

kol, phase 1/2, head and neck squamous cell carcinoma, hnscc, +4 more
8 terms
kol technical
"it will host an in-person and virtual KOL event at the 2026 American"
A KOL, or key opinion leader, is a trusted expert—often a leading physician, researcher, or specialist—whose views influence peers, clinical practice, and industry adoption of medical products or treatments. For investors, KOL endorsements or criticisms can sway adoption rates, regulatory perceptions, and market confidence much like a respected critic can affect demand for a new product, so monitoring KOL sentiment helps gauge commercial and clinical prospects.
phase 1/2 medical
"updated data from the Phase 1/2 clinical study of CRB-701 in 75 participants"
Phase 1/2 is a combined early-stage clinical trial that first tests a new drug or treatment for safety and the right dose, then quickly expands to check if it shows any signs of working in patients. For investors, results from a Phase 1/2 study offer an early read on both risk and potential reward—like a prototype test that both confirms a product won’t harm users and suggests whether it could sell—helping guide valuation and development decisions.
head and neck squamous cell carcinoma medical
"data from the Phase 1/2 clinical study of CRB-701 in 75 participants with head and neck squamous cell carcinoma"
A type of cancer that starts in the thin, flat cells that line the mouth, throat, voice box and upper airway; imagine the lining like roof shingles that, when damaged, can grow into a harmful lump. It matters to investors because its diagnosis, treatment options and regulatory approvals drive demand for drugs, tests and therapies—affecting clinical trial outcomes, market size, company valuations and the financial risk/reward of healthcare investments.
hnscc medical
"monotherapy data in HNSCC on June 1, 2026"
HNSCC stands for head and neck squamous cell carcinoma, a type of cancer that starts in the flat lining cells that cover the surfaces of the mouth, throat and related structures. It matters to investors because treatments, clinical trial results, regulatory approvals or changes in diagnosis rates can directly affect the commercial prospects and valuation of companies developing therapies or diagnostics for this disease—think of it as a market signal tied to demand for specific medical products.
pharmacokinetics medical
"Phase 1/2 study has evaluated the safety, pharmacokinetics and efficacy of CRB-701"
Pharmacokinetics is the study of how a substance, such as a drug or chemical, moves through and is processed by the body over time. It tracks how it is absorbed, distributed, broken down, and eventually eliminated. For investors, understanding pharmacokinetics helps gauge the effectiveness, safety, and potential risks of new medications or treatments, which can influence a company’s success and valuation in the healthcare industry.
antibody-drug-conjugate medical
"CRB-701 is a next-generation antibody-drug-conjugate (ADC) targeting Nectin-4"
An antibody-drug-conjugate is a targeted medicine that pairs a disease-seeking antibody with a potent drug so the treatment is delivered directly to affected cells, like a guided missile carrying a warhead to a specific target. For investors it matters because ADCs can offer high-value, precision therapies whose clinical trial results, approvals, manufacturing challenges and pricing decisions can drive big shifts in a drug developer’s revenue and stock value.
adc medical
"next-generation antibody-drug-conjugate (ADC) targeting Nectin-4"
An antibody-drug conjugate (ADC) is a targeted cancer medicine that pairs an antibody that recognizes specific markers on tumor cells with a potent cell-killing drug, connected so the toxic payload is delivered directly to the cancer. For investors, ADCs matter because successful ADCs can improve patient outcomes and reduce side effects compared with traditional chemotherapy, shaping clinical trial success, regulatory approval chances, commercial demand, and a company’s valuation much like a guided missile versus a general bomb.
mmae medical
"homogenous drug antibody ratio of 2, using MMAE as the payload"
MMAE (monomethyl auristatin E) is a potent synthetic cell‑killing molecule commonly used as the toxic “payload” attached to antibodies in targeted cancer treatments called antibody‑drug conjugates. For investors, MMAE matters because its potency, safety profile, manufacturing complexity and patent status directly affect a therapy’s effectiveness, side effects and commercial viability—think of it as the engine in a guided missile that must be powerful but precisely delivered to avoid collateral damage.

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

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KOL Panel to Discuss Updated CRB-701 Monotherapy Data in HNSCC on June 1, 2026

NORWOOD, Mass., May 05, 2026 (GLOBE NEWSWIRE) -- Corbus Pharmaceuticals Holdings, Inc. (NASDAQ: CRBP), a clinical-stage company focused on promising new therapies in oncology and obesity, today announced that it will host an in-person and virtual KOL event at the 2026 American Society of Clinical Oncology (ASCO) annual meeting to discuss updated data from the Phase 1/2 clinical study of CRB-701 in 75 participants with head and neck squamous cell carcinoma (HNSCC).

Data will include clinical response durability as well as HNSCC patient subgroup analysis. These data will be presented as a poster at the 2026 ASCO annual meeting, to be held May 29 – June 2, 2026 in Chicago, IL.

The KOL event will be held at the Marriott Marquis Chicago starting at 6:30AM CT on Monday, June 1st. The event will feature insights from leading HNSCC experts:

  • Ari Rosenberg, MD – University of Chicago Medicine
  • Glenn Hanna, MD - Dana-Farber Cancer Institute
  • Cesar Augusto Perez Batista, MD - Sarah Cannon Research Institute

A live question and answer session will follow the formal presentation and discussion. To register for either virtual or in-person attendance, click here.

The ongoing three-part Phase 1/2 study has evaluated the safety, pharmacokinetics and efficacy of CRB-701 in 317 participants with advanced solid tumors associated with high Nectin-4 expression. CRB-701 is a next-generation antibody-drug-conjugate (ADC) targeting Nectin-4, that contains a site-specific, cleavable linker and a homogenous drug antibody ratio of 2, using MMAE as the payload.

Corbus recently announced broad alignment with the FDA on the registration path for CRB-701 in HNSCC.

About Ari Rosenberg, MD
Ari Rosenberg, MD, is a medical oncologist and Associate Professor of Medicine at the University of Chicago who specializes in using basic, translation and clinical research to improve the lives of his patients. As a clinical investigator, Dr. Rosenberg focuses on developing novel therapeutic strategies, including immunotherapy, for patients with head and neck cancer and thyroid cancer. He is also establishing methods to reduce treatment-related toxicity for better outcomes and quality of life. In 2025, Dr. Rosenberg was named to the prestigious list of 40 Under 40 in Cancer, an award that recognizes him as one of the nation's most promising young oncology professionals and celebrates his contributions to improve the lives of those affected by cancer.

About Glenn Hanna, MD
Glenn Hanna, MD, completed his fellowship training in hematology and medical oncology at Dana-Farber Cancer Institute in 2016. Prior to this, he earned his medical degree from Georgetown University School of Medicine in 2010, where he graduated summa cum laude, a member of Alpha Omega Alpha Honor Society and the Kober Medalist for academic excellence. He joined the faculty of the Center for Head and Neck Oncology in 2017. Dr. Hanna is the Director of the Center for Cancer Therapeutic Innovation (CCTI), the early drug development program at DFCI. His clinical and translational research efforts focus on precision medicine approaches to treat head and neck cancers. He has special interests in salivary gland cancers and rare head and neck malignancies, and in molecular and immunologic biomarker discovery.

About Cesar Augusto Perez Batista, MD
Cesar Augusto Perez Batista, MD, is Director of the Drug Development Unit at Sarah Cannon Research Institute at Florida Cancer Specialists in Lake Nona, Florida. A recognized cancer expert, he leads early-phase trials for solid tumors with a focus on head and neck cancer and serves as Executive Chair of the Head and Neck Cancer Research Group for the Sarah Cannon Network. He has served on several ASCO head and neck committees and is an ASCO Ambassador. Dr. Perez is an Affiliate Associate Professor at the University of Central Florida and previously co-led Phase 1 and head and neck oncology research at the University of Miami, following earlier faculty work at the University of Louisville, where he twice earned the Best Faculty Teacher Award. He trained at the Cleveland Clinic and the University of Miami, where he was Chief Fellow and received the Peter A. Cassileth, MD Award. He is board certified in medical oncology, hematology, and internal medicine.

About CRB-701
CRB-701 (SYS6002) is a next-generation antibody drug conjugate (ADC) targeting Nectin-4, that contains a site-specific, cleavable linker and a homogenous drug antibody ratio of 2, using MMAE as the payload. Nectin-4 is a clinically validated, tumor-associated antigen in urothelial cancer. The FDA has granted two Fast Track designations to CRB-701 in HNSCC and cervical cancer. CRB-701 is licensed from CSPC Megalith Biopharmaceutical Co. Ltd. China.

About Corbus
Corbus Pharmaceuticals Holdings, Inc. is a clinical-stage company focusing on promising 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, 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, market opportunity, competitive position, possible or assumed future results of operations, business strategies, potential growth opportunities 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. 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.

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


FAQ

When and where will Corbus (CRBP) host the CRB-701 KOL event at ASCO 2026?

The KOL event is on June 1, 2026 at Marriott Marquis Chicago starting at 6:30 AM CT. According to Corbus, the session will be both in-person and virtual and follows a poster presentation at ASCO May 29–June 2, 2026.

What CRB-701 data will Corbus (CRBP) present at ASCO 2026 and the June 1 KOL event?

Corbus will present updated Phase 1/2 CRB-701 data focused on response durability and HNSCC subgroup analyses. According to Corbus, the poster and KOL discussion will include results from 75 HNSCC participants within the broader 317-participant study.

Who are the speakers at the Corbus (CRBP) CRB-701 KOL event during ASCO 2026?

The KOL panel includes Ari Rosenberg, MD; Glenn Hanna, MD; and Cesar Augusto Perez Batista, MD. According to Corbus, these HNSCC experts will present clinical insights followed by a live question-and-answer session.

How many participants has the CRB-701 program evaluated and in which tumor types, per Corbus (CRBP)?

The ongoing three-part Phase 1/2 program has evaluated CRB-701 in 317 participants with advanced solid tumors tied to high Nectin-4 expression. According to Corbus, 75 of those participants are HNSCC patients included in the updated data.

What is CRB-701 and what is Corbus (CRBP) saying about regulatory progress for HNSCC?

CRB-701 is a Nectin-4–targeting antibody-drug conjugate using MMAE with a homogeneous drug-antibody ratio of 2. According to Corbus, the company recently announced broad alignment with the FDA on a registration path in HNSCC.