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| Press Releases |
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| Wednesday, July 8, 2020 |
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Eisai: New Drug Application for In-House Developed New Anti-insomnia Drug Dayvigo Accepted in Hong Kong |
| Eisai Co., Ltd. announced today that the new drug application for approval of its in-house-discovered and developed orexin receptor antagonist DAYVIGO (generic name: lemborexant) for the treatment of adults with insomnia, characterized by difficulties with sleep onset and/or sleep maintenance, has been accepted by the Hong Kong Department of Health. more info >> |
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| Wednesday, June 13, 2018 |
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Eisai to Establish New Research Facility "Eisai Center for Genetics Guided Dementia Discovery" in Cambridge, Massachusetts, USA |
| Eisai Co., Ltd. has announced that it has decided to establish the Eisai Center for Genetics Guided Dementia Discovery (G2D2), a new exploratory research facility focused on immuno-dementia based on human genetics, aimed at innovative drug discovery in the field of dementia, in Cambridge, Massachusetts, the United States. more info >> |
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エーザイ、米国マサチューセッツ州ケンブリッジに新たな研究所Eisai Center for Genetics Guided Dementia Discoveryを設立 |
| エーザイ株式会社は、このたび米国マサチューセッツ州ケンブリッジに、認知症領域での革新的創薬を志向したヒト遺伝学（Human Genetics）に基づく認知症神経免疫療法（Immuno-Dementia）にフォーカスした新たな探索研究所（Eisai Center for Genetics Guided Dementia Discovery）を設立することを決定しましたのでお知らせします。 more info >> |
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| Monday, June 11, 2018 |
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アッヴィ・エーザイ・EAファーマ、ヒト型抗ヒトTNFαモノクローナル抗体「ヒュミラ(R)」とオート・インジェクター製剤「ヒュミラ(R)皮下注ペン」を新発売 |
| アッヴィ合同会社とエーザイ株式会社およびその消化器事業子会社であるEAファーマ株式会社は、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」）のオート・インジェクター製剤「ヒュミラ(R)皮下注40mgペン0.4mL」、および「ヒュミラ(R)皮下注80mgペン0.8mL」について、5月30日に薬価基準に収載されたことを受け、本日、発売したことをお知らせいたします。 more info >> |
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AbbVie and Eisai Announce the Launch of HUMIRA Pen, an Auto-Injector Formulation for Fully Human Anti-TNF-alpha Monoclonal Antibody HUMIRA |
| The newly launched pen-type auto-injector devices were developed to simplify the operation and reduce the burden on patients when performing self-injection. more info >> |
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| Wednesday, June 6, 2018 |
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エーザイとPurdue Pharma、レンボレキサントの最新データを第32回米国睡眠学会年次総会にて発表 |
| エーザイ株式会社（本社：東京都、代表執行役CEO：内藤晴夫、以下 エーザイ）とPurdue Pharma L.P.(本社：米国コネチカット州、President and CEO：Craig Landau、以下 Purdue Pharma)は、2018年6月2日から6日まで米国メリーランド州ボルチモアで開催された第32回米国睡眠学会（SLEEP2018）年次総会において、睡眠と覚醒を調節する薬剤として現在開発中のレンボレキサントに関する2つの臨床第I相試験(108試験および106試験)の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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Eisai: Positive New Data on Investigational Lemborexant Presented at 32nd Annual SLEEP Meeting |
| Eisai Co., Ltd. and Purdue Pharma L.P. presented the results of two key Phase I clinical studies (Study 108 and Study 106) of their investigational sleep/wake regulation agent lemborexant at the 32nd Annual Meeting of the Associated Professional Sleep Societies (SLEEP 2018), from June 2 to 6 in Baltimore, Maryland, the United States. more info >> |
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| Tuesday, June 5, 2018 |
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エーザイとバイオジェン・インク、Elenbecestatの軽度認知障害および軽度から中等度のアルツハイマー病を対象とした臨床第II相試験の18カ月トップラインにおいて安全性と忍容性を確認 |
| エーザイ株式会社とバイオジェン・インクは、このたび、経口βサイト切断酵素（BACE）阻害剤elenbecestat（開発コードE2609）について、米国で実施した臨床第II相試験（202試験）において、安全性と良好な忍容性を示すとともに、アミロイドPETによる脳内アミロイドベータ（Aβ）レベルの統計学的に有意な減少を示したことをお知らせします。 more info >> |
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Eisai: PhaseII Clinical Study of Elenbecestat Demonstrate Safety and Tolerability in MCI and Mild to Moderate Alzheimer's Disease at 18-Months |
| Eisai Co., Ltd. and Biogen Inc. announced today that elenbecestat was generally safe and well tolerated in a Phase II clinical study (Study 202) of the oral BACE (beta amyloid cleaving enzyme) inhibitor elenbecestat (development code: E2609) conducted in the United States, and the results demonstrated a statistically significant difference in amyloid beta (AB) levels in the brain measured by amyloid-PET (positron emission tomography). more info >> |
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| Monday, June 4, 2018 |
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Eisai and Merck Announce Data at 2018 ASCO Annual Meeting |
| The data are included in presentations at the 54th Annual Meeting of the American Society of Clinical Oncology (ASCO) in Chicago from June 1-5. LENVIMA and KEYTRUDA are not approved for use in combination in any cancer types today. more info >> |
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| Latest Press Releases |
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