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| Friday, January 19, 2018 |
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Eisai: Oral Antifungal Agent NAILIN Capsules 100mg Approved in Japan |
| Sato Pharmaceutical Co., Ltd. obtained marketing and manufacturing approval for the oral antifungal agent NAILIN Capsules 100mg containing the active ingredient fosravuconazole L-lysine ethanolate (fosravuconazole) for the treatment of onychomycosis in Japan on January 19, 2018. more info >> |
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Eisai Enters into Licensing Agreement with Adlai Nortye for Potential Anticancer Agent E7046 |
| Eisai Co., Ltd. announced today that it has entered into a licensing agreement granting exclusive rights concerning the research, development, manufacture and marketing of Eisai's in-house discovered potential anticancer agent E7046. more info >> |
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| Thursday, January 18, 2018 |
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Eisai: Patent Infringement Litigation for Antiemetic Agent ALOXI in the United States |
| Eisai has announced today that the United States Court of Appeals for the Federal Circuit, in the patent infringement lawsuit for antiemetic agent ALOXI (palonosetron hydrochloride) injection has denied Helsinn's petition for rehearing en banc. more info >> |
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エーザイ、制吐剤「ALOXI(R)」に関する米国の特許侵害訴訟について |
| エーザイ、制吐剤「ALOXI(R)」に関する米国の特許侵害訴訟について more info >> |
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| Thursday, January 11, 2018 |
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エーザイ、中国の新蘇州工場において固体剤生産棟が竣工 |
| 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、中国子会社である衛材（中国）薬業有限公司（Eisai China Inc.）が、蘇州工業園区内の新蘇州工場において、固体剤生産棟と管理棟を竣工しましたのでお知らせします。 more info >> |
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Eisai Completes Construction of Oral Solid Dose Production Facility at New Suzhou Plant in China |
| Eisai Co., Ltd. announced today that its Chinese subsidiary, Eisai China Inc. has completed construction of a new oral solid dose production facility and an administration building at the site of its new Suzhou plant located within the Suzhou Industrial Park. more info >> |
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| Tuesday, January 9, 2018 |
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Biogen and Eisai Commence Co-Promotion of Multiple Sclerosis Treatments in Japan |
| Eisai Co., Ltd. and Biogen Japan Ltd. announced that the companies have commenced co-promotion of Biogen Japan's multiple sclerosis treatments TECFIDERA (dimethyl fumarate), TYSABRI (natalizumab, genetic recombinant) and AVONEX (interferon beta 1a, genetic recombinant) in Japan as of today. more info >> |
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Eisai and Merck & Co. Receive Breakthrough Therapy Designation from U.S. FDA for LENVIMA and KEYTRUDA |
| The LENVIMA and KEYTRUDA combination therapy is being jointly developed by Eisai and MSD. This is the second Breakthrough Therapy Designation for LENVIMA and the twelfth Breakthrough Therapy Designation granted to KEYTRUDA. more info >> |
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エーザイとMSD、「レンビマ」と「キイトルーダ」併用療法について米国FDAよりブレイクスルーセラピーの指定を受領 |
| エーザイ株式会社（本社：東京都、代表執行役 CEO：内藤晴夫）と Merck & Co., Inc., Kenilworth, N.J., U.S.A.（NYSE：MRK、米国とカナダ以外では MSD）は、このたび、エーザイ創製のマルチキナーゼ阻害剤「レンビマ(R)」（一般名：レンバチニブメシル酸塩）と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進行性または転移性腎細胞がんの適応に対して、米国食品医薬品局（FDA）よりブレイクスルーセラピーの指定を受けましたのでお知らせします。 more info >> |
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バイオジェンとエーザイが多発性硬化症治療剤の共同販促を開始 |
| バイオジェンとエーザイが多発性硬化症治療剤の共同販促を開始 more info >> |
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