drugset / Trial / NCT03475706

Evaluation of the Efficacy and Safety of Solabegron Tablets for Treatment of Overactive Bladder in Adult Women

NCT03475706

Phase 2 Completed 438 enrolled Velicept Therapeutics, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a Phase 2b, multicenter, randomized, double-blind, placebo-controlled, parallel-group study designed to evaluate the efficacy, safety, and tolerability of solabegron immediate release low dose or high dose tablets, compared to matched placebo, administered twice daily for 12 weeks to adult female subjects with overactive bladder symptoms (frequency, urgency, and predominantly urgency incontinence) for at least 6 months.

Timeline

Start
2018-02-19
Primary completion
2019-01-24
Completion
2019-01-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Solabegron Unknown Oral

Indications