drugset / Trial / NCT00742833

A Phase II Study of KUC-7483 in Patients With Overactive Bladder

NCT00742833

Phase 2 Completed 400 enrolled Kissei Pharmaceutical Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

To investigate the efficacy and safety of KUC-7483 in overactive bladder patients.

Timeline

Start
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Ritobegron Small molecule

Indications