drugset / Trial / NCT03756974

BX-1 in Spasticity Due to Multiple Sclerosis

NCT03756974

Phase 3 Completed 397 enrolled Bionorica SE
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To investigate the efficacy and safety of orally administered BX-1 compared to placebo in patients with spasticity due to multiple sclerosis not sufficiently controlled by current anti-spasticity medication

Timeline

Start
2019-02-18
Primary completion
2021-03-30
Completion
2021-03-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Dronabinol Other / unclassified Oral

Indications

No indication recorded.