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eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that it will take over by transfer the manufacturing and marketing approval of parkinson’s disease treatment equfina® 50mg tablets (safinamide mesilate, “equfina”) in japan from meiji seika pharma co., ltd. (headquarters: tokyo, “meiji”), effective september 23, 2020.
the 7th “award ceremony for 2020 greater suzhou best employer and employer brand forum” was grandly held in the studio of suzhou radio and television general station recently. eisai china inc. stood out among thousands of participating enterprises with its good employer brand image, excellent performance of employer social responsibilities and excellent employee engagement, and has been awarded the “greater suzhou best employer” award for four consecutive years.
on september 1, 2020, the second hhc summit of eisai china holdings ltd. (hereinafter referred to as “eisai china”) was successfully held in shanghai. feng yanhui, senior vice president of eisai global, president of eisai china, and chairman of eisai china hhc committee, led the senior management team of eisai china and leaders of various departments to attend the summit.
on august 30, 2020, “the 37th china pharmaceutical industry information annual conference2020” hosted by china pharmaceutical industry information center was held in zhuhai, guangdong province, and the conference released the list of the top 100 pharmaceutical enterprises in china in 2019, which attracted much attention from the industry.
sahne medical spray is the first otc drug spray-type lotion containing heparinoid
eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that it has launched sahne® medical spray and sahne® medical cream (both are category-2 otc drugs, “sahne medical”) on august 25, 2020 at pharmacies and drugstores throughout japan, as a new product of the sahne brand lineup which has been a favored hand care for generations.
eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that a total of 10 presentations including the latest data on its in-house discovered orexin receptor antagonist lemborexant (product name: dayvigotm civ) will be given at the 34th annual meeting of the associated professional sleep societies (sleep 2020), to be held virtually from august 27 to 30, 2020.
eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) and msd k.k. (headquarters: tokyo, president: jannie oothuizen, “msd”), a subsidiary of merck & co., inc., kenilworth, n.j., u.s.a., announced today that eisai has submitted an application in japan for the additional indication of treatment of unresectable thymic carcinoma for multiple receptor tyrosine kinase inhibitor lenvima ® (generic name: lenvatinib mesylate). in june 2020, lenvima received orphan drug designation in japan for unresectable thymic carcinoma.
eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) and dena co., ltd.’s subsidiary desc healthcare co., ltd. (headquarters: tokyo, ceo: sho segawa, cmo: kuniaki miyake, “dena”) announced that they have begun provision of the brain performance application “easiit” (non-medical device, referred to below as “easiit app”), for preparation against dementia, on july 28, 2020.
allm inc. (shibuya-ku, tokyo, president: teppei sakano, hereafter allm), tokyo medical and dental university (bunkyo-ku, tokyo, president: yujiro tanaka) and eisai co., ltd. (headquarters: bunkyo-ku, tokyo, ceo: haruo naito, hereafter eisai) announced that their jointly submitted study and development project has been selected by the japan agency for medical research and development (amed) for its publicly advertised 2020 “field of support for experimental study on medical devices and systems that contribute to measures against viruses and other infectious diseases” as part of its “technology development project for measures against viruses and other infectious diseases “, and that allm has entered into an industry-academia-government joint research agreement with tokyo medical and dental university and eisai respectively.
the alzheimer’s clinical trials consortium (actc), eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”), and biogen inc. (nasdaq: biib, headquarters: cambridge, massachusetts, united states, ceo: michel vounatsos, “biogen”) announced today that a new phase iii clinical study (ahead 3-45) of ban2401, an anti-amyloid beta (aβ) protofibril antibody, has been initiated in the united states of america for individuals with preclinical alzheimer’s disease (ad), meaning they are clinically normal and have intermediate or elevated levels of amyloid in their brains.
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