chen, chenyan – page 15 – eisai china lnc.-pg电子app

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that the results of a phase iii trial (study 304) of its in-house discovered and developed anticancer agent lenvatinib mesylate (product names: lenvima® / kisplyx®, “lenvatinib”) against the comparator sorafenib as first-line treatment for unresectable hepatocellular carcinoma, will be orally presented during the 53rd annual meeting of the american society of clinical oncology (asco), taking place in chicago, the united states. in this study, lenvatinib was the first agent to demonstrate statistical non-inferiority against sorafenib in the primary endpoint of overall survival (os) and showed statistically significant and clinically meaningful improvements in the secondary endpoints of progression free survival (pfs), time to progression (ttp), and objective response rate (orr), doubling sorafenib‘s median values and ratios.

on april 19, 2017, eisai china inc. (hereinafter referred to as: eisai (china)) was invited to attend the “health to countryside” activity held in yudu county, jiangxi province by the national committee for education, science, culture, health and sports of chinese people’s political consultative conference (cppcc), and donated medicines worth rmb540,000 yuan to the local hospitals. according to the statistics, eisai (china), practicing the philosophy of hhc (human health care) all along, donated medicines worth rmb450,000, rmb490,000, rmb500,000 and rmb540,000 respectively to this activity from the year 2014 to 2017, with the total worth of medicines reaching up to rmb1.98 million yuan.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) and meiji seika pharma co., ltd. (headquarters: tokyo; ceo: daikichiro kobayashi, “meiji”) announced today that they have entered into a license agreement for the commercialization of safinamide (development code: me2125) for the treatment of parkinson’s disease in japan and asia. safinamide is currently under clinical development by meiji in japan.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai” ) announced today that the german federal joint committee (g-ba) has confirmed the additional benefit of in-house developed anticancer agent kisplyx® (lenvatinib mesylate) in combination with everolimus for the treatment of advanced renal cell carcinoma (rcc) compared to everolimus alone in its assessment for insurance reimbursement. based on this additional benefit assessment, price negotiations with the head association of german sick funds (gkv-sv) will be conducted, and a reimbursement price has to be agreed. 

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito) announced today that, in association with its u.s. pharmaceutical subsidiary eisai inc. (collectively, “eisai”), it has reached an agreement with arena pharmaceuticals, inc. (headquarters: california, united states, president and ceo: amit d. munshi) to revise the november 2013 marketing and supply agreement it concluded with arena’s wholly owned subsidiary, arena pharmaceuticals gmbh (collectively, “arena”), for the chronic weight management treatment lorcaserin hydrochloride (generic name, u.s. brand name: belviq® / belviq xr®, “belviq”). under the new agreement, eisai acquires all of arena’s rights to develop and market belviq.