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Regeneron pharmaceuticals) for the adjuvant treatment of adults with cutaneous squamous cell carcinoma (cscc) who are at a high risk of recurrence following surgery and radiation. Second fda approval for tevimbra in 2024 The fda approves eylea hd the treatment of patients with macular edema following retinal vein occlusion.
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The fda evaluated libtayo under priority review, which is reserved for medicines that represent potentially significant improvements in efficacy or safety in the treatment of serious conditions Full prescribing information for libtayo will be posted on drugs@fda. An additional regulatory application is also under review in the european union, with a decision expected by the first half of 2026.
