drugset / Trial / NCT01565707

A Study to Investigate How Effective and Safe Solifenacin Succinate Suspension is in Treating Children/Adolescents Aged 5 to Less Than 18 Years With Symptoms of Overactive Bladder (OAB) Compared to a Non-active Drug

NCT01565707

Phase 3 Completed 189 enrolled Astellas Pharma Europe B.V.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Solifenacin succinate as a tablet formulation is already on the market for the treatment of symptoms of overactive bladder in adults. For the use in children and adolescent patients a new formulation of solifenacin has been developed. This study investigated the effect and safety of solifenacin succinate liquid suspension compared to a non-active drug (placebo) over a 12-week period. The 2 weeks prior to the double blind period was a single-blind placebo run-in period in combination with behavioral urotherapy (Non-interventional diary assisted urotherapy consisting of overactive bladder (OAB) information, awareness, instruction, life-style advice and documentation of voiding habits and symptoms for OAB), followed by a 12 week daily treatment period. The study also investigated how well solifenacin succinate suspension is taken-up by the body and how long it stays in the body during this time.

Timeline

Start
2012-06-07
Primary completion
2013-12-31
Completion
2014-01-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Solifenacin Small molecule 2.5 mg Oral
Subject Solifenacin Small molecule 5 mg Oral
Subject Solifenacin Small molecule 7.5 mg Oral
Subject Solifenacin Small molecule 10 mg Oral

Indications