drugset / Trial / NCT04815967

Efficacy and Safety Study of MYOBLOC® in the Treatment of Adult Upper Limb Spasticity

NCT04815967

RandomizedParallel-groupQuadruple-blindTreatment

Summary

Phase 2/3, randomized, double-blind, placebo-controlled, single-treatment, multicenter trial assessing the efficacy and safety of MYOBLOC for the treatment of upper limb spasticity in adults followed by an open-label extension safety trial.

Timeline

Start
2021-11-02
Primary completion
2023-04-23
Completion
2023-04-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum Toxin Type B Unknown 10000 iu Intramuscular
Subject Botulinum Toxin Type B Unknown 15000 iu Intramuscular
Subject Botulinum Toxin Type B Unknown 20000 iu Intramuscular