drugset / Trial / NCT00439140

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

NCT00439140 ↗

Phase 3 Terminated 41 enrolled Allergan
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will assess the safety and efficacy of botulinum toxin Type A for the treatment of urinary incontinence overactive bladder in patients with a spinal cord injury or multiple sclerosis.

Timeline

Start
2007-06
Primary completion
2012-12
Completion
2012-12

Outcome

Outcome not reported

Stopped: “In agreement with FDA the study was terminated based on data available.”

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