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  Press Releases
Wednesday, March 11, 2026
エーザイ、アルツハイマー・パーキンソン病学会(AD/PD 2026)において、レカネマブの長期実臨床治療をはじめとするアルツハイマー病の最新知見を発表
Monday, March 2, 2026
WELIREG(R) (belzutifan) Plus LENVIMA(R) (lenvatinib) Reduced the Risk of Disease Progression or Death by 30% Compared to Cabozantinib in Certain Previously Treated Patients With Advanced Renal Cell Carcinoma (RCC)
エーザイとMerck & Co.,Inc.、「レンビマ(R)」(レンバチニブ)と「ウェリレグ(R)」(ベルズチファン)の併用療法が治療歴のある進行腎細胞がんにおいて、カボザンチニブと比較して、疾患進行または死亡のリスクを30%低減
Monday, February 16, 2026
エーザイ、新規オレキシン受容体作動薬 E2086 が日本において、ナルコレプシーを対象として、厚生労働省より希少疾病用医薬品に指定
Ministry of Health, Labour and Welfare Grants Orphan Drug Designation in Japan to Novel Orexin Receptor Agonist E2086 for Narcolepsy
Tuesday, February 10, 2026
Biologics License Application for Subcutaneous Formulation of "LEQEMBI(R)" (lecanemab) for the Treatment of Early Alzheimer's Disease Designated for Priority Review in China
Friday, February 6, 2026
Eisai and Henlius Enter into Exclusive Commercial License Agreement for Anti-PD-1 Antibody Serplulimab in Japan
Monday, January 26, 2026
FDA Accepts LEQEMBI(R) IQLIK(TM) (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer's Disease under Priority Review
エーザイとバイオジェン、抗 Aβ抗体レカネマブの皮下注射製剤「LEQEMBI(R) IQLIK(TM)」について、早期アルツハイマー病に対する初期療法からの投与を可能とする生物製剤承認一部変更申請が米国 FDA に受理され、優先審査に指定
Wednesday, January 21, 2026
Eisai Listed as a Global 100 Most Sustainable Corporation for the Tenth Time

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