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  Press Releases
Tuesday, June 8, 2021
FDA grants accelerated approval for ADUHELM as the first and only Alzheimer's disease treatment to address a defining pathology of the disease
Eisai: New Data on LENVIMA (lenvatinib) Plus KEYTRUDA (pembrolizumab) Versus Sunitinib
Monday, May 31, 2021
Eisai and ITO EN Enter Into Business Alliance Aiming to Support People Living with Dementia and to Prevent Dementia
Thursday, May 20, 2021
Eisai to Present Data on Oncology Pipeline and Products at ASCO Annual Meeting
Wednesday, May 19, 2021
Anticancer Agent "Remitoro Intravenous Drip Infusion 300 microgram" (Denileukin Diftitox (Genetical Recombination)) Launched in Japan
Friday, May 14, 2021
Eisai and National Cancer Center Commence Joint Research and Development Project
Tuesday, May 11, 2021
Eisai's Statement of Commitment for Carbon Neutrality by 2040
Friday, May 7, 2021
Eisai and Merck & Co., Inc., Kenilworth, N.J., U.S.A. Receive Priority Review From FDA for LENVIMA (lenvatinib) Plus KEYTRUDA (pembrolizumab) Applications
Wednesday, April 28, 2021
RESONA and Eisai Enter Into Business Alliance Aiming to Support People Living with Dementia and to Prevent Dementia in Saitama Prefecture, Japan
Friday, April 23, 2021
Eisai: Application Submitted for Additional Indication of Anti Cancer Agent Lenvima in Combination With Keytruda as a Treatment for Advanced Uterine Body Cancer in Japan

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