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Press release
2022年11月30日 17時30分
Source:
Eisai
エーザイ、11名の先端医療機関の専門家および8名のエーザイ研究者による「レカネマブ」の早期アルツハイマー病に対する臨床第III相Clarity AD検証試験結果の論文がthe New England Journal of Medicineに掲載
東京, 2022年11月30日 - (JCN Newswire) - エーザイ株式会社（本社：東京都、代表執行役CEO：内藤晴夫、以下 エーザイ）とバイオジェン・インク （Nasdaq: BIIB、本社：米国マサチューセッツ州ケンブリッジ、CEO：Christopher A. Viehbacher、以下 バイオジェン）は、このたび、抗アミロイドβ（Aβ）プロトフィブリル抗体レカネマブ（開発品コード：BAN2401）について、脳内アミロイド病理が確認されたアルツハイマー病（AD）による軽度認知障害（Mild Cognitive Impairment：MCI）および軽度AD（これらを総称して早期ADと定義）を対象とした大規模なグローバル臨床第III相Clarity AD検証試験の結果が世界的に最も権威のある医学雑誌の一つである査読学術専門誌the New England Journal of Medicineに掲載されたことをお知らせします。
今回のClarity AD試験結果の迅速な論文化は、エーザイのヒューマンヘルスケア理念に基づく、信頼性、透明性に対する強いコミットメントの証です。引き続き、エーザイとバイオジェンは、レカネマブに関するデータと情報の開示に努め、本剤が承認された際には、必要とする当事者様、ご家族に一刻も早く本剤をお届けできるよう全力を尽くしてまいります。
レカネマブについて、エーザイは、開発および薬事申請をグローバルに主導し、エーザイの最終意思決定権のもとで、エーザイとバイオジェンが共同商業化・共同販促を行います。
本リリースの詳細は下記をご参照ください。
https://www.eisai.co.jp/news/2022/news202284.html
概要：エーザイ株式会社
詳細は www.eisai.co.jp をご覧ください。
Source: Eisai
セクター: バイオテック
Copyright ©2024 JCN Newswire. All rights reserved. A division of Japan Corporate News Network.
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