Year Founded
2017
Ownership
Public
Employees
~310
Stage
Commercial
Modalities
Urovant Sciences General Information
Lead product GEMTESA (vibegron) received FDA approval for overactive bladder. Demonstrated significant reduction in OAB symptoms vs placebo at Week 12 in Phase 3 EMPOWUR study with favorable long-term safety in 40-week extension.
Drug Pipeline
vibegron
CommercialKey Partnerships
Sumitomo Dainippon Pharma, Sunovion, Merck Sharp & Dohme Corp, Ion Channel Innovations
Urovant Sciences Funding
Deal Type | Date | Amount | Status | Stage |
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