drugset / Trial / NCT06782490

A Study to Evaluate the Efficacy, Safety and Tolerability of BMS-986368 in Participants With Multiple Sclerosis Spasticity

NCT06782490

Phase 2 Recruiting 200 enrolled Celgene Corporation
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy, safety, and tolerability of BMS-986368 in participants with Multiple Sclerosis Spasticity

Timeline

Start
2025-06-05
Primary completion
2027-05-26
Completion
2027-06-09

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-986368 Unknown Oral

Indications