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  Press Releases
Monday, October 18, 2021
Eisai and Merck & Co., Inc. (Kenilworth, N.J.) Receive Positive EU CHMP Opinions for LENVIMA (lenvatinib) Plus KEYTRUDA (pembrolizumab) in Two Different Types of Cancer
Tuesday, September 28, 2021
Eisai Initiates Rolling Submission to the U.S. FDA for Biologics License Application of Lecanemab (BAN2401) for Early Alzheimer's Disease Under the Accelerated Approval Pathway
Monday, September 27, 2021
Eisai: Fully Human Anti-TNFalpha Monoclonal Antibody HUMIRA Obtains Additional Approval
Tuesday, September 14, 2021
Eisai to Join The Global Environmental Initiative "RE100"
Eisai to Present Abstracts on Oncology Products and Pipeline at ESMO Virtual Congress 2021
Monday, September 13, 2021
AbbVie, Eisai, and EA Pharma Launch "Humira Support Tool Ordering Service for Patients"
Tuesday, August 31, 2021
Eisai and FUJI YAKUHIN Conclude License Agreement Concerning the Development and Distribution of Dotinurad in Five ASEAN Countries
Monday, August 16, 2021
Anticancer Agent "Tazverik Tablets 200mg" (Tazemetostat Hydrobromide) Launched in Japan for EZH2 Gene Mutation-Positive Follicular Lymphoma
Thursday, August 12, 2021
FDA Approves LENVIMA (lenvatinib) Plus KEYTRUDA (pembrolizumab) Combination for First-Line Treatment of Adult Patients with Advanced Renal Cell Carcinoma (RCC)
Thursday, August 5, 2021
Eisai Receives Award for Excellence in Corporate Communications at the 37th Corporate Communications Awards

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