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| Thursday, March 7, 2019 |
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Eisai's Marketing Authorization Application for Potential Insomnia Disorder Treatment Lemborexant Submitted in Japan |
| Eisai Co., Ltd. announced today that a marketing authorization application has been submitted in Japan for lemborexant, an investigational agent for sleep-wake regulation, seeking approval for use in the treatment of insomnia disorder. more info >> |
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| Wednesday, February 27, 2019 |
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エーザイ、国際NGO「難民を助ける会」とスーダンでの活動を支援する契約を締結 |
| 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、日本の国際NGOである「特定非営利活動法人 難民を助ける会（Association for Aid and Relief, Japan）」（本部：東京都、理事長：長有紀枝、 以下 AAR Japan）がスーダンにおいて展開する菌腫（マイセトーマ）に対する啓発事業を支援する契約を締結したことをお知らせします。 more info >> |
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Eisai Enters Into Agreement to Support International Ngo Association for Aid and Relief, Japan's Activities in Sudan |
| Eisai Co., Ltd. has entered an agreement to support the international non-governmental organization Association for Aid and Relief, Japan's program to raise awareness of mycetoma in Sudan. more info >> |
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| Thursday, February 21, 2019 |
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アッヴィとエーザイ、ヒト型抗ヒトTNFαモノクローナル抗体「ヒュミラ(R)」について国内で初めて化膿性汗腺炎の適応追加承認を取得 |
| アッヴィ合同会社（本社：東京都、社長：ジェームス・フェリシアーノ、以下 アッヴィ）とエーザイ株式会社（本社：東京都、代表執行役CEO：内藤晴夫、以下 エーザイ）は、ヒト型抗ヒトTNFαモノクローナル抗体「ヒュミラ(R)」（一般名：アダリムマブ＜遺伝子組換え＞、以下「ヒュミラ」）について、化膿性汗腺炎（Hidradenitis Suppurativa：HS）の適応追加承認を本日取得したことをお知らせします。 more info >> |
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AbbVie and Eisai Announce Fully Human Anti-TNF-alpha Monoclonal Antibody HUMIRA is the First in Japan to be Approved for the Treatment of Hidradenitis Suppurativa |
| AbbVie, a research-based global biopharmaceutical company and Eisai Co., Ltd. announced that they have received approval for an additional indication of HUMIRA (generic name: adalimumab [recombinant]), a fully human anti-TNF-alpha monoclonal antibody, for the treatment of hidradenitis suppurativa (HS). more info >> |
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| Wednesday, February 13, 2019 |
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エーザイ、抗てんかん剤「Fycompa(R)」について欧州において小児てんかんに係る適応で承認申請を提出 |
| エーザイ株式会社（本社：東京都、代表執行役CEO：内藤晴夫）は、このたび、自社創製の抗てんかん剤「Fycompa(R)」（一般名：ペランパネル、日本製品名：「フィコンパ(R)」)について、欧州医薬品庁（EMA）に対して、小児てんかんに係る適応拡大の追加申請を行いましたのでお知らせします。 more info >> |
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Eisai Submits Application in Europe Seeking Approval for Fycompa as Treatment for Pediatric Patients With Epilepsy |
| Eisai Co., Ltd. announced today that it has submitted an application to the European Medicines Agency (EMA) for its in-house discovered antiepileptic drug (AED) Fycompa (perampanel) seeking approval for use in pediatric patients with epilepsy. more info >> |
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エーザイ、人事異動ならびに組織改編（2019年2月12日付）を発表 |
| エーザイ株式会社は12日、人事異動ならびに組織改編（2019年2月12日付）を以下のとおり発表しました。 more info >> |
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| Monday, February 4, 2019 |
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Eisai and Purdue Pharma Present Efficacy and Safety Data from Second Pivotal Phase 3 Study |
| Eisai Co., Ltd. and Purdue Pharma L.P. announced a six-month results from SUNRISE 2, a long-term Phase 3 clinical study evaluating the efficacy and safety of lemborexant, an investigational agent being developed for the treatment of insomnia, a sleep-wake disorder. more info >> |
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| Tuesday, February 20, 2024 |
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Eisai Selected for 'Human Capital Leaders 2023' and 'Human Capital Management Gold Quality', Recognized as Company Committed to Excellent Management and Disclosure of Human Capital Initiatives |
| Eisai Co., Ltd. announced today that it has been selected for "Human Capital Leaders 2023" and "Human Capital Management Gold Quality" in the "Human Capital Survey 2023" jointly conducted by HR Technology Consortium, HR Research Institute (ProFuture Inc.) and MS&AD InterRisk Research & Consulting, Inc. more info >> |
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