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| Friday, February 28, 2025 |
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Eisai Enters into License Agreement for the Development and Distribution of Fibroblast Growth Factor (FGF) Receptor Selective Tyrosine Kinase Inhibitor Tasurgratinib in Greater China Region (Mainland China, Hong Kong, Macau, and Taiwan) with SciClone |
| Eisai will maintain the rights to tasurgratinib worldwide outside of the licensed regions and continue to manufacture and market it in Japan, where it has been already launched. more info >> |
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エーザイ、線維芽細胞増殖因子受容体（FGFR）選択的チロシンキナーゼ阻害剤タスルグラチニブについて中国・香港・マカオ・台湾での開発・販売に関するライセンス契約をSciCloneと締結 |
| 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、自社創製の線維芽細胞増殖因子受容体（FGFR）選択的チロシンキナーゼ阻害剤タスルグラチニブコハク酸塩（一般名、開発コード：E7090、日本製品名：「タスフィゴ®」、以下、タスルグラニチブ）について、SciClone Pharmaceuticals (Holdings) Limited（本社：中国上海市、以下、SciClone）に、中国・香港・マカオ・台湾（以下、当該ライセンス地域）における開発、販売に関する独占的権利を供与するライセンス契約を締結したことをお知らせします。 more info >> |
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| Thursday, February 20, 2025 |
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エーザイ、優れた人的資本経営・情報開示に取り組む企業として「人的資本リーダーズ 2024」「人的資本経営品質 ゴールド」に2年連続で選出 |
| エーザイ株式会社（本社：東京都、代表執行役CEO：内藤晴夫）は、一般社団法人HRテクノロジーコンソーシアムとHR総研（ProFuture株式会社）、MS＆ADインターリスク総研株式会社、一般社団法人人的資本と企業価値向上研究会が共同で実施した「人的資本調査 2024」において、「人的資本リーダーズ 2024」ならびに「人的資本経営品質 ゴールド」に選出されたことをお知らせします。今回は昨年に続く2回目の選出となります。 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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エーザイ、ASCO GI および ASCO GU において複数のがんに対する最新の開発研究に関する演題を発表 |
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| Thursday, January 11, 2024 |
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Eisai: The Scientific Advisory Group (SAG) to Convene to Discuss the Marketing Authorization Application for lecanemab in the EU |
| Eisai Co., Ltd. announced today that the Scientific Advisory Group (SAG) will convene to discuss the marketing authorization application (MAA) of lecanemab (generic name, brand name: LEQEMBI), which is currently under review by the European Medicines Agency (EMA). more info >> |
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