drugset / Trial / NCT00366002

Patient's Perception of Treatment Outcome With Darifenacin by Patients With Overactive Bladder

NCT00366002

Phase 4 Completed 500 enrolled Novartis Procter and Gamble · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study will evaluate safety, efficacy and patient's perception of outcome after treatment with darifenacin (7.5 mg once daily (o.d.) with voluntary increase up to 15 mg o.d.) in patients with OAB who are dissatisfied with prior oxybutynin extended release (ER) or tolterodine extended release (ER) therapy.

Timeline

Start
2006-06
Primary completion
Completion
2007-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Darifenacin Small molecule 7.5 mg
Subject Darifenacin Small molecule 15 mg

Indications