The Cancer Letter

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Drugs & Targets

FDA accepts sBLA and grants Priority Review for Bavencio + Inlyta in RCC

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EMD Serono and Pfizer Inc. announced the FDA has accepted for Priority Review the supplemental Biologics License Application for Bavencio (avelumab) in combination with Inlyta (axitinib) for patients with advanced renal cell carcinoma. The application has been given a target action date in June 2019.

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