Checkpoint Therapeutics Announces Confirmation of Registration Path for Cosibelimab in Metastatic Cutaneous Squamous Cell Carcinoma

FDA feedback supports plan to submit Biologics License Application (BLA) based on data from ongoing Phase 1 trial One-third enrollment complete in cohort of patients with metastatic cutaneous squamous cell carcinoma Potential for cosibelimab to be differentiated and lower-cost alternative to available anti-PD-1/L1 mAbs

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