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eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that it will launch its first food with function claims chocola bb® rich ceramide (notification number: b60) in drugstores, pharmacies and convenience stores throughout japan on monday, october 17. the product is japan’s first drink that is a type of food with function claims containing glucosylceramide derived from rice.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that its u.s. subsidiary eisai inc. has launched belviq xr® 20mg tablets, a new once-daily formulation of belviq® (generic name: lorcaserin hydrochloride) for chronic weight management in the united states.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today the initiation of a global phase iii clinical study (study 307, clear study) of its in-house developed multiple receptor tyrosine kinase inhibitor lenvatinib mesylate (lenvatinib) in respective combination regimens with the anticancer agent everolimus and the anti-pd-1 antibody pembrolizumab as a potential first-line treatment for advanced renal cell carcinoma.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that a series of abstracts highlighting the latest clinical and pre-clinical data on lenvatinib mesylate (selective inhibitor of receptor tyrosine kinases (rtks) with a novel binding mode, product name: lenvima®/kisplyx®, “lenvatinib”) and eribulin mesylate (halichondrin class microtubule dynamics inhibitor, product name: halaven®, “eribulin”) will be presented during the european society for medical oncology (esmo) congress 2016, taking place in copenhagen, denmark, from october 7 – 11.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced that its european regional headquarters eisai europe ltd. (location: u.k.) has received license from the european commission for anticancer agent kisplyx® ▼ (generic name: lenvatinib mesylate, “lenvatinib”) in combination with everolimus for the treatment of adult patients with advanced renal cell carcinoma following one prior vascular endothelial growth factor (vegf) targeted therapy. following the united states, europe marks the second region where lenvatinib has been licensed for the advanced renal cell carcinoma indication.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that it has been selected for a fourth consecutive year of membership in the dow jones sustainability asia pacific index (djsi asia pacific), the asia pacific version of the dow jones sustainability indices (djsi), which are a family of premier global indices for socially responsible investment (sri).

on september 3rd 2016, the peripheral neuropathy forum is successfully held by eisai china inc. in changsha, china.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that it will launch “chocola bb® mouth ulcer repair shot” (third-class otc drug) for mouth ulcers in japan on thursday, august 25. the product is the first oral care spray to be marketed under the chocola bb brand.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that, at its recent meeting with the u.s. food and drug administration (fda), the fda confirmed there was sufficient data to support the advancement of its novel investigational oral beta-secretase cleaving enzyme (bace) inhibitor e2609 into phase iii clinical studies. e2609 was discovered by eisai and is being jointly developed by eisai and biogen inc. (headquarters: massachusetts, united states, ceo: george a. scangos, “biogen”) for early alzheimer’s disease.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that its european regional headquarters eisai europe ltd. (location: u.k.) has received a positive opinion from the european medicines agency’s committee for medicinal products for human use (chmp) on anticancer agent lenvatinib mesylate (generic name, “lenvatinib”) in combination with everolimus for the treatment of adult patients with advanced renal cell carcinoma (rcc) following one prior vascular endothelial growth factor (vegf) targeted therapy. if approved, lenvatinib will be launched under the brand name kisplyx® for this indication.

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