drugset / Trial / NCT03583372

An Extension Study to Examine the Safety and Tolerability of a New Drug in Patients With Symptoms of Overactive Bladder (OAB).

NCT03583372

Phase 3 Completed 506 enrolled Urovant Sciences GmbH
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is designed to evaluate the safety, tolerability, and efficacy of vibegron administered once daily in participants with OAB for up to 52 weeks.

Timeline

Start
2018-06-14
Primary completion
2019-06-13
Completion
2019-07-25

Drugs

EvaluationDrugModalityDoseRoute
Comparator Tolterodine Small molecule 4 mg
Subject Vibegron Unknown 75 mg

Indications