drugset / Trial / NCT01274000

A Study to Evaluate Efficacy of YM060 on Diarrhea-predominant Irritable Bowel Syndrome (D-IBS) in Female Patients

NCT01274000

Phase 2 Completed 409 enrolled Astellas Pharma Inc
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A study to verify the superiority of YM060 (ramosetron) to placebo for female patients with diarrhea-predominant irritable bowel syndrome (D-IBS) and to evaluate its safety.

Timeline

Start
2010-11
Primary completion
2011-10
Completion
2011-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Ramosetron Small molecule 1.25 ug Oral
Subject Ramosetron Small molecule 2.5 ug Oral
Subject Ramosetron Small molecule 5 ug Oral