Myovant Sciences Announces European Commission Approval for RYEQO? for the Treatment of Women With Uterine Fibroids
- RYEQO is the first and only once-daily long-term treatment for uterine fibroids in Europe
- Indication has no limitation for duration of use, as supported by safety and efficacy data from the Phase 3 LIBERTY program
- Gedeon Richter?to commercialize RYEQO, starting in the second half of 2021; Myovant to receive a regulatory milestone payment and is eligible to receive tiered royalties on net sales as well as sales milestone payments
- Marketing authorization application for RYEQO for endometriosis-associated pain on track for submission this calendar year