chen, chenyan – page 11 – eisai china lnc.-nba直播小9直播

 chen, chenyan – page 11 – eisai china lnc.-nba直播小9直播

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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 to present latest data on alzheimer’s disease / dementia pipeline at 11th clinical trials on alzheimer’s disease conference

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”).

eisai and purdue pharma announce positive topline results of sunrise 2, the second phase 3 pivotal study of lemborexant

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.

new drug application for perampanel for adjunctive treatment of partial onset seizures accepted in china

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

lenvima® (lenvatinib) capsules approved for first-line treatment of unresectable hepatocellular carcinoma (hcc) in south korea

lenvima® (lenvatinib mesylate) as a single agent for the first-line treatment of patients with unresectable hepatocellular carcinoma (hcc) from the ministry of food and drug safety (mfds) in south korea. an application seeking approval of lenvima for use in the treatment of unresectable hcc was submitted in south korea in march 2018. this approval for lenvima in south korea marks the second in asia following approval in japan. lenvima is the first new treatment option approved in ten years as a first-line systemic treatment for hcc in south korea.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) has announced that results from the cardiovascular outcomes trial (camellia-timi 61) in patients treated with lorcaserin hydrochloride (generic name, product name in the u.s.: belviq®, “belviq”) were highlighted in an oral presentation at the european society of cardiology (esc) congress 2018 held in munich, germany, and concurrently published in the new england journal of medicine, one of the world’s most influential medical journals.1 belviq is the first ever weight loss medication approved for chronic weight management which has been proven to not increase the incidence of major cardiovascular (cv) events in a dedicated long-term cardiovascular outcome trial.

tokyo august 23, 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 european commission (ec) has granted a marketing authorization for the oral receptor tyrosine kinase (rtk) inhibitor lenvima® (lenvatinib mesylate) as a single agent for the first-line treatment of adult patients with advanced or unresectable hepatocellular carcinoma (hcc) who have received no prior systemic therapy. this is the first new first-line treatment option for advanced or unresectable hcc to be approved in europe in approximately 10 years.

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