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| Press Releases |
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| Friday, September 29, 2017 |
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Eisai Presents Results of Phase Iii Trial of Lenvima (Lenvatinib) in Unresectable Hepatocellular Carcinoma in Oral Session at 20th CSCO Annual Meeting |
| In the subpopulation analysis, lenvatinib demonstrated efficacy based on extension of Overall Survival (OS) compared to sorafenib (nominal P = 0.026), with improvements also observed in Progression Free Survival (PFS), Time to Progression (TTP) and Objective Response Rate (ORR) (see table below). more info >> |
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| Wednesday, September 27, 2017 |
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Eisai: Application for Additional Indication of Lenvima for Hepatocellular Carcinoma Accepted for Review by U.S. FDA |
| This application is based on the results of the REFLECT study (Study 304), a multicenter, open-label, randomized, global Phase III trial comparing the efficacy and safety of Lenvima versus sorafenib, a standard treatment for HCC, as a first-line treatment for patients with unresectable HCC. more info >> |
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| Friday, September 22, 2017 |
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エーザイ: プロトンポンプ阻害剤「パリエット(R)錠5mg、錠10mg」 日本でプロトンポンプ阻害剤抵抗性の逆流性食道炎に対する維持療法の用法・用量追加の承認を取得 |
| エーザイ株式会社とエーザイの消化器事業子会社であるEAファーマ株式会社は、本日、エーザイが、日本において、プロトンポンプ阻害剤 「パリエット(R)錠5mg、錠10mg」（一般名 ：ラベプラゾールナトリウム）について、プロトンポンプ阻害剤抵抗性 逆流性食道炎（プロトンポンプ阻害剤の1日1回投与による従来の治療で効果不十分な逆流性食道炎）に対する維持療法に関して、ラベプラゾールナトリウムとして1回10mg 1日2回投与の用法・用量追加の承認を取得したことをお知らせします。 more info >> |
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エーザイ初の抗体薬物複合体MORAb-202に関する最新の非臨床試験データを第8回World ADC年次総会において発表 |
| エーザイ株式会社（本社：東京都、代表執行役 CEO：内藤晴夫）は、このたび、当社の研究開発会社であるモルフォテック・インクが創製したエーザイ初の抗体薬物複合体（Antibody-Drug Conjugate：ADC）である MORAb-202 に関する最新非臨床試験データを、「第 8 回 World ADC 年次総会」において発表しましたので、お知らせします。 more info >> |
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Eisai: Additional Dosage and Administration of Proton Pump Inhibitor Pariet 5 mg Tablets, 10 mg Tablets Approved in Japan for Maintenance Therapy of Proton Pump Inhibitor Resistant Reflux Esophagitis |
| Eisai Co., Ltd. and Eisai's subsidiary for gastrointestinal disease area EA Pharma Co., Ltd. announced today that Eisai has obtained the approval of additional dosage and administration in Japan of the proton pump inhibitor Pariet 5 mg Tablets and 10 mg Tablets to administer 10 mg of rabeprazole sodium per dose twice-daily for the maintenance therapy of proton pump inhibitor-resistant reflux esophagitis. more info >> |
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Eisai Presents Latest Non-Clinical Data on Its First Antibody-Drug Conjugate MORAb-202 at 8th Annual World ADC |
| Eisai Co., Ltd. announced today that the latest non-clinical data on MORAb-202, Eisai's first antibody-drug conjugate (ADC) developed by its research subsidiary Morphotek, Inc., was presented at the 8th Annual World ADC. more info >> |
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| Friday, March 11, 2022 |
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Eisai to Present New Lecanemab Data Exploring Distinct Mechanism of Action and Clinical Outcomes, Disease State (DSE) Symposium, and Other Pipeline Assets at the AD/PD 2022 Annual Meeting |
| Eisai Co., Ltd. announced today the company will present research from its robust Alzheimer's disease (AD) pipeline, including the latest findings on lecanemab, Eisai's investigational anti-amyloid beta (Abeta) protofibril antibody for the treatment of early AD at the AD/PD 2022 International Conference on Alzheimer's and Parkinson's Diseases (AD/PD) from March 15-20 in Barcelona, Spain and virtually. more info >> |
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| Wednesday, March 9, 2022 |
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Eisai Certified as the 2022 Health and Productivity Management Outstanding Organization (White 500) |
| Eisai Co., Ltd. announced today that it has been certified as the Health and Productivity Management Outstanding Organization in the large enterprise category (White 500) by Japan's Ministry of Economy, Trade and Industry and the Nippon Kenko Kaigi. more info >> |
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| Monday, March 7, 2022 |
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LENVIMA in Combination with KEYTRUDA Approved In Taiwan for the Treatment of Patients with Advanced Endometrial Carcinoma |
| Eisai Co., Ltd. announced today that LENVIMA (generic name: lenvatinib mesylate), the multiple receptor tyrosine kinase inhibitor discovered by Eisai, in combination with Merck & Co., Inc., Kenilworth, N.J., U.S.A. more info >> |
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エーザイ、「レンビマ(R)」「キイトルーダ(R)」との併用療法について、治療ラインに関らず全身療法後に増悪した、根治的手術または放射線療法に不適応な進行性子宮内膜がんの適応で、台湾において承認を取得 |
| 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、このたび、自社創製のチロシンキナーゼ阻害剤「レンビマ(R)」（一般名：レンバチニブメシル酸塩）について、Merck & Co., Inc. Kenilworth, N.J., U.S.A.（北米以外ではMSD）の抗PD-1抗体「キイトルーダ(R)」（一般名：ペムブロリズマブ）との併用療法による治療ラインに関らず全身療法後に増悪した、根治的手術または放射線療法に不適応な進行性子宮内膜がんの適応で、台湾において承認を取得したことをお知らせします。 more info >> |
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| Latest Press Releases |
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Hong Kong Vocational Education Service in Joint Construction of the 'Belt and Road' Vocational Education Symposium
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Summit Group Responds to White Paper Citing Governance Issues in Bangladesh's Power and Energy Sector
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The 2024 PropertyGuru Asia Property Awards International Luncheon celebrates real estate achievements in the Middle East and South Asia
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