drugset / Trial / NCT04099667

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

NCT04099667

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 lower limb spasticity, in adults followed by an open-label extension safety trial.

Timeline

Start
2019-12-17
Primary completion
2023-03-24
Completion
2023-03-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum Toxin Type B Unknown 15000 iu Intramuscular
Subject Botulinum Toxin Type B Unknown 20000 iu Intramuscular
Subject Botulinum Toxin Type B Unknown 25000 iu Intramuscular

Indications

No indication recorded.