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

NCT06782490

This study is recruiting at 14 US sites in 12 states, according to its ClinicalTrials.gov record last updated .

Summary

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

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Multiple Sclerosis Spasticity

Eligibility basics and study details

Study type
Interventional
Phase
Phase 2
Ages
18 to 70 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
Celgene
Last updated on ClinicalTrials.gov
October 1, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Alabama · 1

  • Alabama Neurology Associates · Birmingham, AL

Arizona · 1

  • Perseverance Research Center,LLC · Scottsdale, AZ

Florida · 2

  • Aqualane Clinical Research · Naples, FL
  • USF Health · Tampa, FL

Kansas · 1

  • University of Kansas Medical Center · Kansas City, KS

Massachusetts · 1

  • Neurology Center of New England · Foxborough, MA

Michigan · 1

  • Northwest Neurology · Southfield, MI

Missouri · 1

  • Washington University School of Medicine · St Louis, MO

Ohio · 2

  • University of Cincinnati Medical Center · Cincinnati, OH
  • Riverside Methodist Hospital · Columbus, OH

Pennsylvania · 1

  • Thomas Jefferson University, Jefferson Headache Center · Philadelphia, PA

Tennessee · 1

  • Hope Neurology · Knoxville, TN

Texas · 1

  • Prime Clinical Research · Lewisville, TX

Washington · 1

  • EvergreenHealth Medical Center · Kirkland, WA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.