During the treatment period ranging from 8 to 19 months in 5 clinical studies, the incidence of anti-cemiplimab-rwlc antibodies in libtayo-treated patients was 2% (22/1029). On october 8, 2025, the food and drug administration approved cemiplimab-rwlc (libtayo, regeneron pharmaceuticals inc. ) for the adjuvant treatment of adults with cutaneous squamous cell carcinoma Learn about libtayo® (cemiplimab-rwlc) in the treatment of advanced nsclc, bcc, cscc, & as an adjuvant treatment for high-risk cscc.

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