Second approval for Keytruda and Lenvima combination
The US Food and Drug Administration (FDA) has issued a new approval for the combination of Merck & Co’s (NYSE: MRK) anti-PD-1 therapy, Keytruda (pembrolizumab) and Lenvima (lenvatinib), the orally available multiple receptor tyrosine kinase inhibitor discovered by Eisai (TYO: 4523).
This approval is for the first-line treatment of adults with advanced renal cell carcinoma (RCC) and adds to the first indication in endometrial cancer.
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