Pharmamarketeer

Pfizer & Merck’s Inlyta combo becomes first FDA-approved anti-PD-L1 therapy for kidney cancer

The FDA has approved Bavencio (avelumab) in combination with Inlyta (axitinib) for the treatment of advanced renal cell carcinoma (RCC). The decision was announced by the drug’s co-developers Merck KGaA and Pfizer, and marks the first FDA approval for an anti-PD-L1 therapy as part of a combination regimen in this indication.

Around 20-30% of new diagnoses in RCC are made at an advanced stage, and almost a tired of early-stage diagnoses go on to develop metastases, meaning there is a considerable unmet need for first-line treatment which safely delay progression of the disease.

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