Corporate Member Update- Merck: KEYTRUDA® Additional Indication
Corporate Member Update- Merck: KEYTRUDA® Additional Indication
KEYTRUDA®
July, 2020
Merck is pleased to announce that KEYTRUDA® (pembrolizumab) injection 100 mg has been approved by the FDA for the treatment of patients with recurrent or metastatic cutaneous squamous cell carcinoma (cSCC) that is not curable by surgery or radiation. The FDA has also approved KEYTRUDA® (pembrolizumab) for the first-line treatment of patients with unresectable or metastatic MSI-H or dMMR colorectal cancer (CRC).
Please read the updates below for additional information!
KEYTRUDA(R) (pembrolizumab): Additional Indication
KEYTRUDA(R) (pembrolizumab): Additional Indication2