drugset / Trial / NCT04103450

Extension Study of Vibegron in Men With Overactive Bladder (OAB) Symptoms on Pharmacological Therapy for Benign Prostatic Hyperplasia

NCT04103450

Phase 3 Completed 276 enrolled Urovant Sciences GmbH
NaSingle-groupOpen-labelTreatment

Summary

This study will assess the long-term safety of vibegron when dosed up to 52 weeks in men with overactive bladder (OAB) symptoms on pharmacological therapy for Benign Prostatic Hyperplasia (BPH) who previously completed treatment in Study URO-901-3005 (NCT03902080).

Timeline

Start
2019-09-19
Primary completion
2022-07-29
Completion
2022-07-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Vibegron Unknown 75 mg Oral

Indications