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eisai launches lenvima® (lenvatinib) in china

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced that its chinese subsidiary eisai china inc. (eci) has launched the kinase inhibitor lenvima®(product name in china: 乐卫玛®, generic name: lenvatinib mesylate) in china.

november 7, 2018, eisai china inc. (eci) held the inauguration ceremony for its new suzhou plant located at no. 168 xingpu road within the suzhou industrial park. mr. kazuyuki katayama (consulate-general of japan in shanghai), mr. yue wang (commissioner of jiangsu food and drug administration), mr. qingwen wu (standing committee of suzhou municipality and secretary general of the party committee of suzhou industrial park administrative committee (sipac)), ms.  yanyan sun (deputy director of sipac), mr. jianmin chen (director-general of suzhou food and drug administration), dr. haruo naito (ceo of eisai co., ltd.), mr. yasushi okada (representative corporate officer of ecl, industry affairs and china business), ms. yanhui feng (vice president of ecl, president of eisai china), mr. norio kaneko (chairman of eisai china) and people with close attention to the development of eisai china attended the ceremony.

eisai china inc. held the “2018 ads”

on october 27, 2018, the “2018 ads” (ads: advance dementia science) was held by eisai china inc. in beijing, china. the 2018 ads is a communication platform that eisai china established for doctors; the forum covers multi-aspects such as basic researches in the cognitive fields, new methods of diagnosis, clinical hotspots, research and development for new drugs, social and government policies, and etc., with well-known professors from china, japan and south korea discussing and interacting with over 300 participants on-site and over 400 participators online. 

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced that eisai presented new data from study 202, a phase ii evaluation of lemborexant, an investigational sleep-wake regulation agent, for the treatment of irregular sleep-wake rhythm disorder (iswrd) in patients with mild to moderate alzheimer’s disease. the data were presented at the 11th clinical trials in alzheimer’s disease (ctad) conference in barcelona, spain. lemborexant is being developed for the treatment of multiple sleep-wake disorders, including insomnia disorder.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) and biogen inc. (nasdaq: biib) (headquarters: cambridge, massachusetts, united states, ceo: michel vounatsos, “biogen”) announced that eisai presented the latest data from the phase ii clinical study (study 201) of ban2401, an anti-amyloid beta protofibril antibody, in 856 patients with early alzheimer’s disease, at a symposium session titled “clinical and biomarker updates from ban2401 study 201 in early alzheimer’s disease” held on october 25 at the 11th clinical trials on alzheimers disease (ctad) conference in barcelona, spain.

on october 23, 2018, eisai china inc. was invited to attend the “health to countryside” activity held in duyun city, qiannan autonomous prefecture, guizhou province by the national committee for education, science, culture, health and sports of chinese people’s political consultative conference (cppcc), and donated medicines worth rmb510,000 yuan to the local health commission. eisai china acts in accordance with the corporate philosophy of human health care (hhc) and practices social responsibilities all along, donating medicines worth rmb450,000, rmb490,000, rmb500,000, rmb540,000 and rmb510,000 respectively to this project from the year 2014 to 2018, with the total worth of medicines reaching up to approximately rmb2.5 million yuan.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that five oral presentations including a symposium, and two poster presentations, highlighting the latest data on its alzheimer’s disease / dementia pipeline including anti-amyloid beta (aβ) protofibril antibody ban2401, oral beta secretase cleaving enzyme (bace) inhibitor elenbecestat, anti-aβ antibody aducanumab, and dual orexin receptor antagonist lemborexant, will be given at the 11th clinical trials on alzheimer’s disease (ctad) conference taking place in barcelona, spain, from october 24 to 27. ban2401, elenbecestat and aducanumab are being jointly developed by eisai and biogen inc. (headquarters: cambridge, massachusetts, united states, “biogen”).

tokyo and stamford, conn. – october 17, 2018 – eisai co., ltd. (ceo: haruo naito, “eisai”) and purdue pharma l.p. (president and ceo: craig landau, “purdue pharma”) today announced positive topline results from sunrise 2, a long-term phase 3 efficacy and safety evaluation of lemborexant, an investigational agent for sleep-wake regulation currently being studied for the potential treatment of multiple sleep-wake disorders. topline results reported today are the primary and key secondary outcomes of the study from the six-month, placebo-controlled treatment period; the study is ongoing to 12 months. eisai and purdue pharma plan to present full results from sunrise 2 at upcoming medical meetings in 2019.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) has announced that the national medical products administration of china has accepted for review a new drug application for eisai’s antiepileptic drug (aed) perampanel (generic name, product name: fycompa®) as an adjunctive treatment for partial onset seizures in epilepsy patients 12 years of age and older. this nda is the first to be submitted for perampanel in china.

tokyo and kenilworth, n.j. sept. 5, 2018 – eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) and merck & co., inc., kenilworth n.j., u.s.a., known as msd outside of the united states and canada, announced today that the china national medical products administration (nmpa) approved the kinase inhibitor lenvima® (lenvatinib) as a single agent for the treatment of patients with unresectable hepatocellular carcinoma (hcc) who have not received prior systemic therapy. in china, the application of lenvima was submitted in october 2017, and was designated for priority review by the nmpa due to lenvima’s significant clinical benefit compared to existing treatments, leading to approval in approximately 10 months. this approval marks the first for lenvima in china, where the incidence of hcc is high,1 and the first new systemic therapy approved for the first-line treatment of unresectable hcc in china in ten years.1

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