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  Press Releases
Tuesday, May 10, 2022
Eisai Completes Rolling Submission to the U.S. FDA for Biologics License Application of Lecanemab for Early Alzheimer's Disease Under the Accelerated Approval Pathway
Eisai Initiates Preparation for New Drug Application, Based on the Results of an Investigator-Initiated Clinical Trial of Ultrahigh-Dose Mecobalamin for Amyotrophic Lateral Sclerosis in Japan
Friday, April 1, 2022
Eisai Announces Acquisition of Arteryex Shares (Making Arteryex a Subsidiary) to Strengthen and Rapidly Expand the Foundation of its Digital Solution Business
Monday, March 28, 2022
Eisai: Announcement About an Approval for Additional Indication of Jyseleca, JAK inhibitor
Tuesday, March 22, 2022
Eisai: Latest Findings on Lecanemab Presented at AD/PD 2022 Annual Meeting
Tuesday, March 15, 2022
Eisai: Economic Arrangements of Amendment to Alzheimer's Disease Treatment Collaboration Agreement with Biogen
Biogen and Eisai Amend Collaboration Agreements on Alzheimer's Disease Treatments
Friday, March 11, 2022
Eisai to Present New Lecanemab Data Exploring Distinct Mechanism of Action and Clinical Outcomes, Disease State (DSE) Symposium, and Other Pipeline Assets at the AD/PD 2022 Annual Meeting
Wednesday, March 9, 2022
Eisai Certified as the 2022 Health and Productivity Management Outstanding Organization (White 500)
Monday, March 7, 2022
LENVIMA in Combination with KEYTRUDA Approved In Taiwan for the Treatment of Patients with Advanced Endometrial Carcinoma

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