drugset / Trial / NCT00607971
Long-Term Safety of Renzapride in Women With Constipation-Predominant Irritable Bowel Syndrome (IBS-C)
NaSingle-groupOpen-label
Summary
The main purpose of this study is to evaluate the long-term safety and tolerability of renzapride at a dose of 4 mg taken once daily for 12 months in women with constipation-predominant irritable bowel syndrome (IBS-C).
Timeline
- Start
- 2006-04
- Primary completion
- 2008-06
- Completion
- 2008-06
Outcome
Outcome not reported
Stopped: “Terminated due to insufficient efficacy over placebo in Study ATL1251/038/CL.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Renzapride | Small molecule | 4 mg | — |