Clinical Trial SuccessCorbus' CRB-701 is clearly meeting the bar for success in the HNSCC patient population, with a 47.6% ORR at the 3.6 mg/kg dose level among efficacy-evaluable HNSCC patients.
Financial PositionCorbus ended the third quarter with $104.0 million in cash, with an estimated pro forma cash level of about $177.8 million after the recent public offering.
Regulatory ApprovalThe FDA granted Fast Track Designation to CRB-701 in Head and Neck Squamous Cell Carcinoma, marking the second Fast Track designation for this drug.