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FDA Grants Fast Track Designation to Corbus Pharmaceuticals’ Nectin-4 Targeting ADC CRB-701 in Head and Neck Squamous Cell Carcinoma

Dose optimization data from the Phase 1/2 study to be presented next month at ESMO 2025Second Fast Track designation granted by FDA for CRB-701 NORWOOD, Mass., Sept. 16, 2025 (GLOBE NEWSWIRE) -- Corbus Pharmaceuticals Holdings, Inc. (NASDAQ: CRBP) (“Corbus” or the “Company”), a clinical stage oncology and obesity company, announced today that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to CRB-701 for the treatment of recurrent or metastatic head and neck squamo

articleCorbus Pharmaceuticals Holdings, Inc.September 16, 20254/company/corbus-pharmaceuticals-holding/news/fda-grants-fast-track-designation-120000929
FDA Grants Fast Track Designation to Corbus Pharmaceuticals’ Nectin-4 Targeting ADC CRB-701 in Head and Neck Squamous Cell Carcinoma

About this update from Corbus Pharmaceuticals Holdings, Inc.

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More updates from Corbus Pharmaceuticals Holdings, Inc.

Fast Track designationFDAThe CompanyDose optimizationESMOantibody drug conjugatemonoclonal antibodytreatment of obesityForward-Looking Statementsclinical stage