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| Monday, November 6, 2017 |
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New Data From Long-Term Extension of Phase 1B Study of Investigational Alzheimer's Disease Treatment Aducanumab Presented at 10th Clinical Trials on Alzheimer's Disease |
| Eisai Co., Ltd. announced today that Biogen Inc. (Nasdaq: BIIB) presented new data from the long-term extension (LTE) of its ongoing Phase 1b study of aducanumab, an investigational treatment for Alzheimer's disease at the 10th Clinical Trials on Alzheimer's Disease (CTAD) meeting, Boston, Massachusetts, United States, from November 1 to 4. more info >> |
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エーザイ、第10回アルツハイマー病臨床試験会議（CTAD）にてaducanumabの臨床第Ib相試験の長期継続投与に関する最新データを発表 |
| エーザイ株式会社は、2017年11月1日から4日まで米国マサチューセッツ州ボストンで開催された第10回アルツハイマー病臨床試験会議において、当社とバイオジェン・インクがアルツハイマー病の治療薬として共同開発している aducanumab（抗アミロイドβ抗体）について、バイオジェンが実施中の臨床第Ib 相試験の長期継続投与に関する最新データの発表をしたことをお知らせします。 more info >> |
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| Tuesday, October 31, 2017 |
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Eisai's New Drug Application of Anticancer Agent Lenvatinib for Hepatocellular Carcinoma Accepted in China |
| Eisai Co., Ltd. announced that the China Food and Drug Administration (CFDA) has accepted for review a New Drug Application (NDA) submitted for Eisai's in-house discovered and developed anticancer agent lenvatinib mesylate for use in the treatment of hepatocellular carcinoma (HCC) in China. more info >> |
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エーザイ、第10回アルツハイマー病臨床試験会議（CTAD）において、最新の知見を発表 |
| エーザイ株式会社（本社：東京都、代表執行役 CEO：内藤晴夫）は、2017 年 11 月 1 日から 4 日まで米国ボストンで開催される第 10 回アルツハイマー病臨床試験会議（Clinical Trials on Alzheimer's Disease: CTAD）において、lemborexant（経口デュアルオレキシン受容体拮抗剤）および elenbecestat*（経口βサイト切断酵素（BACE）阻害剤）の 2 剤に関する最新の発表をしますのでお知らせします。 more info >> |
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エーザイ: 中国で抗がん剤「レンバチニブ」の肝細胞がんに係る適応による新薬承認申請が受理 |
| エーザイ株式会社（本社：東京都、代表執行役 CEO：内藤晴夫）は、このたび、自社創製の抗がん剤レンバチニブメシル酸塩（一般名、製品名：「レンビマ(R)」 「Kisplyx(R)」、以下 レンバチニブ）について、中国 国家食品薬品監督管理総局に肝細胞がんに係る適応での新薬承認申請を行い、受理されたことをお知らせします。 more info >> |
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| Thursday, February 1, 2024 |
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Eisai Commences Fully-Fledged Business Activities at Pharma Sales Subsidiary in South Africa |
| Eisai Co., Ltd. announced today that fully-fledged operations have begun at Eisai Pharmaceuticals Africa (Pty) Ltd, a pharmaceutical sales subsidiary recently established in Johannesburg, South Africa, and direct sales operations and business activities have commenced in Africa. more info >> |
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| Friday, January 26, 2024 |
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Eisai Submits New Drug Application for Mecobalamin Ultrahigh-Dose Formulation in Japan for the Indication of Amyotrophic Lateral Sclerosis |
| Eisai Co., Ltd. announced today that it has submitted a New Drug Application (NDA) for ultrahigh-dose mecobalamin (development code: E0302) for the indication of amyotrophic lateral sclerosis (ALS) to the Pharmaceuticals and Medical Devices Agency (PDMA) in Japan. more info >> |
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| Thursday, January 18, 2024 |
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Eisai: Antiepileptic Drug Fycompa Injection Formulation Approved in Japan |
| Eisai Co., Ltd. announced today that it has obtained marketing authorization approval from the Japanese Ministry of Health, Labour and Welfare for the injection formulation of its in-house discovered antiepileptic drug (AED) Fycompa (perampanel) in Japan as an alternative therapy when oral administration is temporarily not possible. more info >> |
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| Wednesday, January 17, 2024 |
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Eisai Listed as a Global 100 Most Sustainable Corporation for the Eighth Time |
| Eisai Co., Ltd. announced today that it has been listed in the 2024 Global 100 Most Sustainable Corporations in the World (Global 100), a global ranking by Canada-based media and investment advisory company, Corporate Knights, Inc. more info >> |
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| Tuesday, January 16, 2024 |
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Eisai Furthers Oncology Research Across Multiple Cancers at ASCO GI and ASCO GU 2024 |
| Eisai Co., Ltd. announced today the presentation of oncology research at two upcoming medical meetings taking place in-person in San Francisco, California and virtually. more info >> |
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