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eisai china inc. kicked off the empowering neurology’s future (enf) successfully on mar. 22, 2020. to avoid people gathering during the epidemic period, the forum is held innovatively online to start a brand-new enf season, which will last from march 22ndto april 28th in seven sessions, one session per week.

eisai china escorts you to tide over the crisis

in the face of the epidemic of covid-19, a large number of patients with normal medical needs can not go to hospital to seek medical treatment, and their diseases can not be treated well, which seriously decreases the quality of life of patients. eisai china holdings ltd. is joining hands with all sectors of society to fight against the epidemic, and escorting people to tide over the crisis. 

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) and fuji yakuhin co., ltd. (headquarters: saitama, ceo: masayuki takayanagi, “fuji yakuhin”) announced today that they have concluded a license agreement concerning dotinurad (generic name), a treatment for hyperuricemia and gout discovered by fuji yakuhin, for development and distribution in china.

for its contributions towards patients with liver disease through the eisai-originated orally available kinase inhibitor lenvima®

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that it received the president’s award at the 8th technology management and innovation awards held by the japan techno-economics society (jates)*. the award was presented to eisai for its discovery of the orally available kinase inhibitor lenvima®(generic name: lenvatinib mesylate) and its contributions towards patients with liver disease.

launch of anticancer agent halaven® in china

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that it has launched the in-house developed anticancer agent halaven® (product name in china: 海乐卫®, generic name: eribulin mesylate) in china.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that it has launched the in-house discovered and developed antiepileptic drug (aed) fycompa®, (product name in china: 卫克泰®, generic name perampanel) for use in adjunctive treatment of partial onset seizures (with or without secondarily generalized seizures) in epilepsy patients 12 years of age and older.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) today announced that the u.s. food and drug administration (fda) approved the new drug application for its in-house discovered and developed orexin receptor antagonist dayvigotm(lemborexant). dayvigo was approved for the treatment of insomnia characterized by difficulties with sleep onset and/or sleep maintenance in adults1. in the united states, dayvigo will be commercially available in 5 mg and 10 mg tablets following scheduling by the u.s. drug enforcement administration (dea), which is expected to occur within 90 days.

sysmex corporation (hq: kobe, japan; chairman and ceo: hisashi ietsugu; “sysmex”) and eisai co., ltd. (hq: tokyo, japan; ceo: haruo naito; “eisai”) are pursuing a joint project to develop a method of diagnosing alzheimer’s disease (ad) using blood, presented two posters showing the most recent data from the project. the presentations took place at the 12th clinical trials on alzheimer’s disease (ctad) conference, from december 4 to 7, 2019, in san diego, california. at ctad, sysmex demonstrated on behalf of the two companies the possibility of understanding amyloid pathology in the brain from the brain-derived amyloid beta (aβ) in plasma measured using its protein measurement platform, the hiscl™ series of fully automated immunoassay analyzers.

sysmex corporation (hq: kobe, japan; chairman and ceo: hisashi ietsugu; “sysmex”) and eisai co., ltd. (hq: tokyo, japan; ceo: haruto naito; “eisai”) announced that the most recent data from the project to develop a method of diagnosing alzheimer’s disease (ad) using blood plasma was presented at the 13th clinical trials on alzheimer’s disease (ctad) conference, held virtually from november 4 to 7, 2020.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that the latest information on its in-house discovered and developed eribulin mesylate (halichondrin class microtubule dynamics inhibitor, product name: halaven®, “eribulin”) will be presented during the 42nd san antonio breast cancer symposium (sabcs2019). the symposium will be held from december 10 through 14, 2019, in san antonio, texas in the united states.

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