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KEYTRUDA® (Pembrolizumab)

December 27, 2018April 5, 2020 RR FDA Approvals
Merkel Cell Carcinoma

The FDA on December 19, 2018 granted accelerated approval to KEYTRUDA® for adult and pediatric patients with recurrent locally advanced or metastatic Merkel Cell Carcinoma (MCC). KEYTRUDA® is a product of Merck & Co. Inc.

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HERZUMA® (Trastuzumab-pkrb)
LYNPARZA® (Olaparib)

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