drugset / Trial / NCT01915459

Phase III Study of Botulax® to Treat Post Stroke Upper Limb Spasticity

NCT01915459 ↗

Phase 3 Completed 186 enrolled Hugel
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the safety and efficacy of Botulax® compared to Botox® reducing upper limb muscle tone in post stroke patients.

Timeline

Start
2013-06
Primary completion
2014-05
Completion
2014-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum toxin type A Protein / enzyme biologic 360 iu Intramuscular

Indications