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| Press Releases |
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| Friday, July 30, 2021 |
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エーザイとバイオジェン、アルツハイマー病の初めてのリアルワールド観察臨床第IV相試験となるADUHELM ICARE AD-USの試験デザインをアルツハイマー病協会国際会議2021において発表 |
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エーザイとバイオジェン、Lecanemab（BAN2401）の臨床効果についてアルツハイマー病協会国際会議2021（AAIC2021）のLate Breakingとして発表 |
| Lecanemabの臨床第II相POC試験後のOpen Label Extension試験における18カ月投与の臨床効果に関する予備解析結果をAAIC2021において発表 more info >> |
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Biogen and Eisai Announce Design of ADUHELM ICARE AD-US Study, the First Real-World Observational Phase 4 Study in Alzheimer's Disease at AAIC 2021 |
| Biogen and Eisai Co., Ltd. today announced that Biogen led a late-breaking presentation on the design of the first real-world observational Phase 4 study in Alzheimer's disease called ICARE AD-US, at the Alzheimer's Association International Conference (AAIC). more info >> |
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| Thursday, July 29, 2021 |
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Eisai Listed for 20th Consecutive Year in FTSE4Good Index Series, An Index for Socially Responsible Investment |
| Eisai Co., Ltd. announced today that it has been included in the FTSE4Good Index Series for the 20th consecutive year since its initial inclusion in 2002. more info >> |
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| Tuesday, July 27, 2021 |
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バイオジェンとエーザイ、ADUHELM(TM)の最新データをアルツハイマー病協会国際会議2021（AAIC2021）において発表 |
| バイオジェン・インクとエーザイ株式会社は、2021 年 7 月 26 日から 30 日に米国コロラド州デンバーおよびバーチャルで開催されているアルツハイマー病協会国際会議（Alzheimer's Association International Conference: AAIC）2021 において、両社のアルツハイマー病（AD）の研究ポートフォリオの一部として、ADUHELM(TM)（一般名：アデュカヌマブ）注射 100mg/mL 溶液による臨床試験データに関する 4 つのポスター発表をバイオジェンが行うことをお知らせします。 more info >> |
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Biogen and Eisai Announce ADUHELM (aducanumab-avwa) Data Presentations at Alzheimer's Association International Conference 2021 |
| Biogen (Nasdaq: BIIB) and Eisai Co., Ltd. (Tokyo, Japan) today announced that Biogen, as part of its Alzheimer's disease (AD) research portfolio, will contribute four virtual posters that showcase data from its clinical trials with ADUHELMTM (aducanumab-avwa) injection 100 mg/mL solution at the AAIC. more info >> |
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| Monday, July 26, 2021 |
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エーザイ、「レンビマ(R)」（レンバチニブ）と「キイトルーダ(R)」（ペムブロリズマブ）の併用療法について進行性子宮内膜がんに係る承認を米国FDAより取得 |
| エーザイ、「レンビマ(R)」（レンバチニブ）と「キイトルーダ(R)」（ペムブロリズマブ）の併用療法について進行性子宮内膜がんに係る承認を米国FDAより取得 more info >> |
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| Friday, July 23, 2021 |
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Eisai: FDA Approves LENVIMA (lenvatinib) Plus KEYTRUDA (pembrolizumab) Combination for Patients With Certain Types of Advanced Endometrial Carcinoma |
| Study Results Demonstrated Statistically Significant Improvements in Overall Survival, Progression-Free Survival and Overall Response Rate, Helping to Address a Significant Unmet Need in Advanced Endometrial Carcinoma. more info >> |
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| Wednesday, July 21, 2021 |
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Eisai to Present Latest Data on Pipeline Assets in The Area of Alzheimer's Disease and Dementia at AAIC 2021 |
| Eisai Co., Ltd. announced today that the company will conduct a total of 11 presentations, including the latest data of the investigational anti-amyloid beta (Abeta) protofibril antibody lecanemab (development code: BAN2401) for which the U.S. Food and Drug Administration has granted Breakthrough Therapy designation, at the Alzheimer's Association International Conference (AAIC). more info >> |
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エーザイのアルツハイマー病／認知症領域の開発品に関する最新データをアルツハイマー病協会国際会議 2021（AAIC2021）にて発表 |
| エーザイ株式会社（本社：東京都、代表執行役 CEO：内藤晴夫）は、2021 年 7 月 26 日から 30 日に米国コロラド州デンバーおよびバーチャルで開催されるアルツハイマー病協会国際会議（Alzheimer's Association International Conference：AAIC）2021 において、抗アミロイドβ（Aβ）プロトフィブリル抗体 lecanemab（開発コード：BAN2401）の最新データを含む合計 11 演題を発表することをお知らせします。Lecanemab は、米国食品医薬品局（FDA）よりブレイクスルーセラピーの指定を受けています。 more info >> |
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| Latest Press Releases |
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