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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 An additional regulatory application is also under review in the european union, with a decision expected by the first half of 2026. In a clinical trial, cemiplimab demonstrated superiority to placebo when treating patients with cscc
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. 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 Findings showed cemiplimab reduced the risk of disease recurrence or death by 68% compared with placebo
The fda approves eylea hd the treatment of patients with macular edema following retinal vein occlusion.
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