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Press Releases |
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Monday, June 6, 2022 |
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エーザイ、米国臨床腫瘍学会年次総会において抗体薬物複合体farletuzumab ecteribulinの最新の知見を発表 |
エーザイ、米国臨床腫瘍学会年次総会において抗体薬物複合体farletuzumab ecteribulinの最新の知見を発表 more info >> |
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Friday, June 3, 2022 |
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Eisai to Present Latest Data on Lemborexant at The 36th Annual Sleep 2022 Meeting |
Eisai Co., Ltd. announced a total of seven poster presentations including the latest data on its in-house discovered orexin receptor antagonist lemborexant (product name: DAYVIGO) will be given at the 36th annual meeting of the Associated Professional Sleep Societies (SLEEP 2022), to be held from June 4 to 8, 2022, in Charlotte, NC, the United States. more info >> |
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Friday, May 27, 2022 |
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Eisai Contributes to the Science of Cancer Medicine at ASCO 2022 |
Eisai Co., Ltd. announced today the presentation of research across various types of cancer from its oncology portfolio during the 2022 American Society of Clinical Oncology (ASCO) Annual Meeting (#ASCO22), which is taking place virtually and in-person in Chicago from June 3 to 7. more info >> |
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Eisai: MHLW Grants Orphan Drug Designation in Japan to Mecobalamin Ultrahigh-Dose Formulation with Prospective Indication for Delaying the Progression of Disease and Functional Impairment of ALS |
Eisai Co., Ltd. announced today that it has received orphan drug designation for ultrahigh-dose mecobalamin, with a prospective indication for delaying the progression of disease and functional impairment of amyotrophic lateral sclerosis (ALS), by the Ministry of Health, Labour and Welfare (MHLW). more info >> |
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エーザイ、メコバラミンの高用量製剤がALSの病態及び機能障害の進行抑制を予定される効能又は効果として、厚生労働省より希少疾病用医薬品に指定 |
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、メコバラミンの高用量製剤について、筋萎縮性側索硬化症(Amyotrophic Lateral Sclerosis: ALS)の病態及び機能障害の進行抑制を予定される効能又は効果として、厚生労働省より希少疾病用医薬品に指定されたことをお知らせします。 more info >> |
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エーザイ、米国臨床腫瘍学会年次総会おけるがん領域の開発品・製品に関する発表について |
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Tuesday, May 10, 2022 |
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エーザイ、筋萎縮性側索硬化症(ALS)に対する高用量メコバラミン製剤の医師主導治験の結果を踏まえて、日本における新薬承認申請に向けた作業を開始 |
エーザイ株式会社は、このたび、国立大学法人徳島大学の梶龍兒特命教授(主任研究者)、徳島大学大学院医歯薬学研究部臨床神経科学分野 和泉唯信教授(治験調整医師)らの研究チームが発表した、発症早期の筋萎縮性側索硬化症患者様に対する高用量メコバラミンの有効性、安全性の検証を目的とした「高用量メチルコバラミン(メコバラミン)の筋萎縮性側索硬化症に対する第III相試験-医師主導治験-」の良好な臨床試験結果を受けて、メコバラミン(開発コード:E0302)の高用量製剤について、日本におけるALSに対する新薬承認申請に向けた作業を開始しましたのでお知らせします。 more info >> |
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エーザイ、抗アミロイドβ(Aβ)プロトフィブリル抗体「レカネマブ」について、米国において、迅速承認制度に基づく早期アルツハイマー病に対する生物製剤ライセンス申請の段階的申請を完了 |
エーザイ、抗アミロイドβ(Aβ)プロトフィブリル抗体「レカネマブ」について、米国において、迅速承認制度に基づく早期アルツハイマー病に対する生物製剤ライセンス申請の段階的申請を完了 more info >> |
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Eisai Completes Rolling Submission to the U.S. FDA for Biologics License Application of Lecanemab for Early Alzheimer's Disease Under the Accelerated Approval Pathway |
Eisai Co., Ltd. and Biogen Inc. announced today that Eisai has completed the rolling submission to the U.S. Food and Drug Administration (FDA) of a Biologics License Application (BLA) under the accelerated approval pathway. more info >> |
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Eisai Initiates Preparation for New Drug Application, Based on the Results of an Investigator-Initiated Clinical Trial of Ultrahigh-Dose Mecobalamin for Amyotrophic Lateral Sclerosis in Japan |
Eisai Co., Ltd. today announced that it has initiated preparation on a New Drug Application for ultrahigh-dose mecobalamin. more info >> |
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Latest Press Releases |
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Apr 25, 2024 16:25 JST
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Elevate Your Sleep Game This World Health Day with LAC
Apr 25, 2024 09:00 HKT/SGT
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UNIQLO Sponsors KAWS + Warhol Exhibition Tour, Starting in Pittsburgh
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GA-ASI Selected to Build CCA for AFLCMC
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The South China Sea: A Nuanced Understanding Required
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Kontent.ai Introduces Mission Control and New Brand Identity, Leading a New Era of Content Management
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业聚医疗合资企业在中国内地启动TricValve临床试验
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