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tokyo and stamford, conn. – march 12, 2019 – eisai co., ltd. (ceo: haruo naito, “eisai”) and imbrium therapeutics l.p. (imbrium therapeutics), a clinical-stage biopharmaceutical company and operating subsidiary of purdue pharma, l.p. (president and ceo: craig landau, md) today announced that the u.s. food and drug administration (fda) has accepted for review the new drug application (nda) for lemborexant, an investigational agent being studied for the treatment of insomnia, a sleep-wake disorder. a prescription drug user fee act (pdufa) date is set for december 27, 2019.

tokyo and stamford, conn. – february 4, 2019 – eisai co., ltd. (ceo: haruo naito, “eisai”) and purdue pharma l.p. (president and ceo: craig landau, md, “purdue pharma”) today announced six-month results from sunrise 2, a long-term phase 3 clinical study evaluating the efficacy and safety of lemborexant, an investigational agent being developed for the treatment of insomnia, a sleep-wake disorder. data were presented at the sleep research society’s advances in sleep and circadian science conference, taking place in clearwater beach, florida, feb. 1-4, 2019.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that it has been listed in the 2019 global 100 most sustainable corporations in the world (global 100), a global ranking by canada-based media and investment advisory company, corporate knights, inc. this marks eisai’s fourth inclusion on the list. ranked 73rd, eisai was the highest ranking japanese company among the eight japanese companies listed in the global 100.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced that its in-house discovered and developed antiepileptic drug (aed) perampanel (generic name, product name: fycompa®), for which  a new drug application (nda) was submitted for review as an adjunctive treatment for partial onset seizures in epilepsy patients 12 years of age and older in china in october 2018, has been designated for priority review by the national medical products administration (nmpa) due to perampanel’s significant clinical benefit compared to existing treatments.