LENVIMA® (Lenvatinib) September 16, 2018April 5, 2020 RR FDA Approvals Liver Cancer (Hepatocellular) The FDA on August 16, 2018 approved LENVIMA® capsules for the first-line treatment of patients with unresectable HepatoCellular Carcinoma (HCC). LENVIMA® is a product of Eisai Inc. Related Posts:LENVIMA® (Lenvatinib)KEYTRUDA® (Pembrolizumab) and LENVIMA® (Lenvatinib)LENVIMA® (Lenvatinib) plus KEYTRUDA® (Pembrolizumab)KEYTRUDA® (Pembrolizumab) in combination with…FDA Approves LENVIMA® for Unresectable…LENVIMA® Plus KEYTRUDA® for Advanced Renal…