drugset / Trial / NCT00290563
Safety and Efficacy of MK0594 to Treat Overactive Bladder (0594-003)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Serlopitant | Small molecule | 0.25 mg | — |
| Subject | Serlopitant | Small molecule | 1 mg | — |
| Subject | Serlopitant | Small molecule | 4 mg | — |