drugset / Trial / NCT00290563

Safety and Efficacy of MK0594 to Treat Overactive Bladder (0594-003)

NCT00290563 ↗

Phase 2 Completed 557 enrolled Vyne Therapeutics Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is designed to investigate whether a new drug may offer safe and effective treatment for patients with overactive bladder.

Timeline

Start
2006-02-21
Primary completion
2007-08
Completion
2007-09-24

Outcome

Met primary endpoint

paper Serlopitant (0.25 and 4 mg) significantly decreased the primary end point of daily micturitions but not the secondary end points compared with placebo. PMID 20639026 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Serlopitant Small molecule 0.25 mg —
Subject Serlopitant Small molecule 1 mg —
Subject Serlopitant Small molecule 4 mg —

Indications