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eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that three oral presentations and eight poster presentations, highlighting the latest data on its alzheimer’s disease / dementia pipeline including anti-amyloid beta (aβ) protofibril antibody ban2401, orexin receptor antagonist lemborexant and a simple blood diagnostic for alzheimer’s disease (ad), will be given at the 12th clinical trials on alzheimer’s disease (ctad) conference taking place in san diego, california in the united states, from december 4 to 7, 2019. ban2401 is being jointly developed by eisai and biogen inc.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) has announced that lenvima (generic name: lenvatinib), the orally available kinase inhibitor discovered by eisai, has been accepted by the national medical products administration of china for an application for the additional indication of differentiated thyroid cancer. this application for additional indication marks the second in china following the indication for hepatocellular carcinoma, which was approved in september 2018.   

eisai china inc. (hereinafter referred to as “eisai china”) successfully held the launch meeting of fycompa® (perampanel) in china on december 1, 2019, which marks the official launch of the new third-generation antiepileptic drug of fycompa® in china. this means that the first non-competitive ampa receptor antagonist is officially ushered in the field of epilepsy treatment in china, which will bring new treatment methods and means for the majority of patients with epilepsy and their families.

mr. yamada koki, deputy general manager of eisai (china) pharmaceutical co., ltd. (hereinafter referred to as “eisai china”), attended the 2018-2019 annual awards ceremony for advanced collectives and outstanding individuals in peking university health science center, on behalf of eisai china, on november 26, 2019. a total of 40 students won the eisai china scholarships for their outstanding performance, and 10 students got the eisai china grants during this academic year. eisai china has awarded scholarships and grants to outstanding students at peking university health science center for 8 consecutive years.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that the latest data on its antiepileptic drug (aed) perampanel (product name: fycompa®) will be presented at the 73rd american epilepsy society annual meeting (aes 2019) to be held from december 6 to december 10, 2019 in baltimore, maryland in the united states.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that it has entered into an agreement to transfer the rights to receive royalties on the sales outside of japan for an investigational anti-cancer agent tazemetostat (generic name) to royalty pharma (headquarters: new york, united states).

cambridge, mass. and tokyo, japan – october 22, 2019 – biogen (nasdaq: biib) and eisai, co., ltd. (tokyo, japan) today announced that, after consulting with the u.s. food and drug administration (fda), biogen plans to pursue regulatory approval for aducanumab, an investigational treatment for early alzheimer’s disease (ad).

eisai china successfully held “2019 ads beijing “

on october 19, 2019, the “2019 ads beijing” sponsored by eisai china inc. was held in beijing, which is another platform for doctors’ information exchanges. featuring the theme of “let’s build hope together”, the main forum and three sub-forums focused on the latest cutting-edge academic research and clinical practice and development in china and in the world. 37 well-known experts and scholars from china, japan, singapore, spain and other countries, more than 300 on-site guests and nearly 1,000 on-line guests jointly discussed and conducted dialogues and interactions, producing collision of ideas and academic resonance between china and foreign countries. 

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today thateisai received a new drug approval for its in-house discovered and developed antiepileptic drug (aed) fycompa® (perampanel) from the china national medical products administration (nmpa) for use in an adjunctive treatment of partial onset seizures (with or without secondarily generalized seizures)in epilepsy patients 12 years of age and older. fycompa was designated for priority review by the nmpa due to itssignificant clinical benefits compared to existing treatments, and was approved in about 12 months since the submission in september 2018.

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