drugset / Trial / NCT01745094

A Study to Evaluate the Effect of Mirabegron + Solifenacin in Overactive Bladder Patients

NCT01745094

Phase 4 Completed 223 enrolled Astellas Pharma Inc
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study was to evaluate the safety and efficacy of mirabegron as add-on therapy in patients with OAB treated with solifenacin.

Timeline

Start
2012-10-01
Primary completion
2013-07-23
Completion
2013-07-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Mirabegron Other / unclassified 25 mg Oral
Subject Mirabegron Other / unclassified 50 mg Oral
Background Solifenacin Small molecule 2.5 mg Oral
Background Solifenacin Small molecule 5 mg Oral

Indications