drugset / Trial / NCT00268879

Investigation of the Safety and Efficacy of Renzapride in Constipation Predominant Irritable Bowel Syndrome (IBS)

NCT00268879 ↗

Phase 3 Completed 1821 enrolled Alizyme
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to investigate whether renzapride will help alleviate the symptoms associated with constipation predominant irritable bowel syndrome in female patients.

Timeline

Start
2005-12
Primary completion
2008-01
Completion
2008-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Renzapride Small molecule 2 mg Oral
Subject Renzapride Small molecule 4 mg Oral