drugset / Trial / NCT00461292

Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurogenic Overactive Bladder

NCT00461292 ↗

Phase 3 Completed 275 enrolled Allergan
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the safety and effectiveness of botulinum toxin type A in treating overactive bladder in spinal cord injury or multiple sclerosis patients

Timeline

Start
2007-05
Primary completion
2010-03
Completion
2010-04

Outcome

Met primary endpoint

paper At week 6, onabotulinumtoxinA 200 U and 300 U significantly reduced UI episodes per week (-21.8 and -19.4, respectively) compared with placebo (-13.2; p<0.01); PMID 21798658 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum toxin type A Protein / enzyme biologic 200 iu Other
Subject Botulinum toxin type A Protein / enzyme biologic 300 iu Other

Indications