drugset / Trial / NCT01852058

A Long-Term Extension Study of OnabotulinumtoxinA (BOTOX®) for Urinary Incontinence Due to Neurogenic Detrusor Overactivity

NCT01852058 ↗

Phase 3 Completed 95 enrolled Allergan
Non-randomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the long-term safety and efficacy of onabotulinumtoxinA (botulinum toxin Type A; BOTOX®) for the treatment of urinary incontinence due to neurogenic detrusor overactivity in participants who successfully completed Study 191622-120 (NCT01852045).

Timeline

Start
2014-01-11
Primary completion
2018-11-22
Completion
2019-10-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum toxin type A Protein / enzyme biologic 50 iu Intramuscular
Subject Botulinum toxin type A Protein / enzyme biologic 100 iu Intramuscular
Subject Botulinum toxin type A Protein / enzyme biologic 200 iu Intramuscular

Indications

No indication recorded.