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Checkpoint Therapeutics Announces Topline Results From Registration-Enabling Trial Of Cosibelimab In Metastatic Cutaneous Squamous Cell Carcinoma; Study Met Primary Endpoint With 47.4% Objective Response Rate

Study met primary endpoint with 47.4% objective response rate Safety and tolerability profile consistent with previously reported data Planned BLA submission on track for later this year Conference call to

CKPT