drugset / Trial / NCT03289702

CORETOX® in Treatment of Post Stroke Upper Limb Spasticity (Phase3)

NCT03289702

Phase 3 Completed 220 enrolled Medy-Tox
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of CORETOX® in the treatment of post-stroke upper limb spasticity

Timeline

Start
2017-11-13
Primary completion
2018-06-30
Completion
2018-11-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator Botulinum toxin type A Protein / enzyme biologic
Subject CORETOX® Unknown

Indications

No indication recorded.