Takeda Pharmaceutical Co. Ltd. has reported the first Phase III data for the investigational uterine fibroid treatment relugolix in Japanese patients in a study that is seen as a bellwether for larger international studies being undertaken by licensee Myovant Sciences Ltd.
The US firm licensed rights to the product outside Japan and certain other Asian countries in June 2016 for use in endometriosis, uterine fibroids and hormone-sensitive prostate cancer. Success for Myovant would in turn take some pressure off its parent company, Roivant Sciences GMBH, after the recent failure of sister firm Axovant Sciences' Phase III Alzheimer's trial with intepirdine. (Also see "Takeda Continues To Shed Pipeline Assets In Roivant Deal" - Scrip, 7 June, 2016
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