Corbus Pharmaceuticals announced FDA Fast Track designation for CRB-701, targeting metastatic cervical cancer with a Phase 1 trial ongoing.
Quiver AI Summary
Corbus Pharmaceuticals Holdings, Inc. announced that the FDA has granted Fast Track designation to its next-generation antibody drug conjugate, CRB-701, for treating relapsed or refractory metastatic cervical cancer. This ADC targets Nectin-4 and utilizes a specific linker and drug-to-antibody ratio for effective delivery. The company recently completed the dose escalation phase of its Phase 1 clinical trial, which assesses the safety and efficacy of CRB-701 in patients with advanced tumors expressing high levels of Nectin-4. Corbus expects to share initial data from this trial in Q1 2025. The company focuses on innovative scientific approaches to combat serious illnesses through its diversified portfolio, which also includes additional investigational therapies for cancer and obesity.
Potential Positives
- The FDA granted Fast Track designation to CRB-701 for treating relapsed or refractory metastatic cervical cancer, potentially accelerating its development and review process.
- Completion of enrollment in the Phase 1 clinical trial for CRB-701 indicates progress in the company's drug development pipeline.
- The upcoming report of data from the clinical study expected in Q1 2025 may attract investor interest and increase visibility in the oncology sector.
- Corbus Pharmaceuticals is advancing its innovative portfolio in oncology and obesity, highlighting its commitment to addressing unmet medical needs in serious illnesses.
Potential Negatives
- The press release heavily relies on forward-looking statements, indicating a level of uncertainty regarding the outcomes of clinical trials and potential market success, which could undermine investor confidence.
- The expectation to report clinical data in Q1 2025 may suggest a prolonged timeline for stakeholders awaiting results, potentially impacting the company's current valuation and investment attractiveness.
- The mention of unmet medical needs highlights the severity of conditions the company is addressing, but it may also reflect on the high-risk nature of their drug development efforts, raising concerns about the viability of their product pipeline.
FAQ
What is CRB-701 and its significance?
CRB-701 is a next-generation antibody drug conjugate targeted for treating relapsed or refractory metastatic cervical cancer.
What does FDA's Fast Track designation mean?
The Fast Track designation facilitates the development and expedites the review of drugs for serious conditions with unmet medical needs.
What is the status of CRB-701's clinical trial?
Corbus has completed enrollment in the dose escalation phase of the Phase 1 clinical trial for CRB-701 and expects data in Q1 2025.
What types of cancer does CRB-701 target?
CRB-701 specifically targets cancers with high Nectin-4 expression, focusing on advanced solid tumors.
Where is Corbus Pharmaceuticals headquartered?
Corbus Pharmaceuticals is headquartered in Norwood, Massachusetts.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$CRBP Insider Trading Activity
$CRBP insiders have traded $CRBP stock on the open market 18 times in the past 6 months. Of those trades, 6 have been purchases and 12 have been sales.
Here’s a breakdown of recent trading of $CRBP stock by insiders over the last 6 months:
- ASSET MANAGEMENT, LP CORMORANT has traded it 6 times. They made 6 purchases, buying 350,000 shares and 0 sales.
- SEAN F. MORAN (Chief Financial Officer) has traded it 4 times. They made 0 purchases and 4 sales, selling 18,043 shares.
- YUVAL COHEN (Chief Executive Officer) has traded it 8 times. They made 0 purchases and 8 sales, selling 63,358 shares.
To track insider transactions, check out Quiver Quantitative's insider trading dashboard.
$CRBP Hedge Fund Activity
We have seen 71 institutional investors add shares of $CRBP stock to their portfolio, and 58 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- ORBIMED ADVISORS LLC added 912,552 shares (+inf%) to their portfolio in Q3 2024
- OCTAGON CAPITAL ADVISORS LP added 627,000 shares (+128.5%) to their portfolio in Q3 2024
- TANG CAPITAL MANAGEMENT LLC added 600,000 shares (+inf%) to their portfolio in Q3 2024
- CORMORANT ASSET MANAGEMENT, LP added 350,000 shares (+17.3%) to their portfolio in Q3 2024
- CITADEL ADVISORS LLC removed 332,761 shares (-100.0%) from their portfolio in Q3 2024
- DARWIN GLOBAL MANAGEMENT, LTD. removed 325,140 shares (-100.0%) from their portfolio in Q3 2024
- WOODLINE PARTNERS LP removed 249,259 shares (-100.0%) from their portfolio in Q3 2024
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.
Full Release
NORWOOD, Mass., Dec. 03, 2024 (GLOBE NEWSWIRE) -- Corbus Pharmaceuticals Holdings, Inc. (NASDAQ: CRBP) (“Corbus” or the “Company”), an oncology and obesity company with a diversified portfolio, announced today that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to CRB-701 for the treatment of relapsed or refractory metastatic cervical cancer. CRB-701 (SYS6002) is a next-generation antibody drug conjugate (ADC) targeting Nectin-4 that contains a site-specific, cleavable linker and a precise drug antibody ratio of 2 using MMAE as the payload.
The FDA’s Fast Track designation is designed to facilitate the development and expedite the review of drugs intended to treat serious conditions that demonstrate the potential to fill an unmet medical need.
Corbus recently completed enrollment of the dose escalation part of its Phase 1 clinical trial of CRB-701 (SYS6002) ( NCT06265727 ) that is being conducted in the U.S. and Europe. The three-part Phase 1 trial is evaluating the safety, pharmacokinetics and efficacy of CRB-701 in patients with advanced solid tumors known to be associated with high Nectin-4 expression. The Company expects to report the first data from the dose escalation clinical study in Q1 2025.
About Corbus
Corbus Pharmaceuticals Holdings, Inc. is an oncology and obesity company with a diversified portfolio 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 that targets the expression of Nectin-4 on cancer cells to release a cytotoxic payload, CRB-601, an anti-integrin monoclonal antibody which blocks the activation of TGFβ expressed on cancer cells, and CRB-913, a highly peripherally restricted CB1 receptor inverse agonist for the treatment of obesity. Corbus is headquartered in Norwood, Massachusetts. For more information on Corbus, visit
corbuspharma.com
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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, 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.
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INVESTOR CONTACT:
Sean Moran
Chief Financial Officer
Corbus Pharmaceuticals
[email protected]
Bruce Mackle
Managing Director
LifeSci Advisors, LLC
[email protected]