Merck, known as MSD outside the United States and Canada, and Eisai announced that the U.S. Food and Drug Administration has issued a Complete Response Letter regarding Merck’s and Eisai’s applications seeking accelerated approval of KEYTRUDA, Merck’s anti-PD-1 therapy, plus LENVIMA, the orally available multiple receptor tyrosine kinase inhibitor discovered by Eisai, for the first-line treatment of patients with unresectable hepatocellular carcinoma.
July 8, 2020
· 50 min read