English | 简体中文 | 繁體中文 | 한국어 | 日本語
  Press Releases
Monday, March 6, 2023
FDA Accepts Eisai's Filing of a Supplemental Biologics License Application and Grants Priority Review for Traditional Approval of LEQEMBITM (lecanemab-irmb) for the Treatment of Alzheimer's Disease
エーザイ、「LEQEMBI」についてアルツハイマー病治療薬としてフル承認に向けた生物製剤承認一部変更申請(sBLA)が米国FDAに受理され、優先審査に指定
Thursday, March 2, 2023
バイオジェン・ジャパンとエーザイの日本における多発性硬化症治療剤の共同販促について
Biogen Japan and Eisai Provide Update on Co-Promotion Of Multiple Sclerosis Treatments In Japan
Wednesday, July 31, 2019
エーザイ、E2082の臨床第I相試験(治験)における死亡例の発生について
Tuesday, February 28, 2023
Biologics License Application for Lecanemab Designated for Priority Review by China National Medical Products Administration
エーザイとバイオジェン、抗アミロイドβプロトフィブリル抗体「レカネマブ」の中国における生物ライセンス申請(BLA)が優先審査に指定
Tuesday, February 21, 2023
Dissolution of Bracco-Eisai Joint Venture
Monday, February 20, 2023
ブラッコ・エーザイの合弁解消について
Monday, January 30, 2023
Lecanemab Receives Priority Review Status in Japan

Copyright © 2026 ACN Newswire - Asia Corporate News Network
Home | About us | Services | Partners | Events | Login | Contact us | Cookies Policy | Privacy Policy | Disclaimer | Terms of Use | RSS
US: +1 214 890 4418 | China: +86 181 2376 3721 | Hong Kong: +852 8192 4922 | Singapore: +65 6549 7068 | Tokyo: +81 3 6859 8575