A Study of Ranolazine in ALS
Start Date
4/29/2025
Completion Date
7/1/2028
Summary
The purpose of this study is to evaluate safety, effect on cramps, function and quality of life of ranolazine versus placebo for the treatment of ALS.
Detailed Description
A prospective, multi center, double-blind, placebo-controlled, parallel group study of 2 doses of ranolazine (500 mg and 1000 mg twice daily) compared to placebo in patients with ALS. Approximately 72 adults with ALS will be enrolled into the study in the United States at approximately 7 ALS treatment sites. Participants will take oral ranolazine or placebo twice daily, attend a minimum of 5 onsite research visits, and 4 remote research visits. The study is estimated to last 28 weeks for each participant.
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
Ranolazine
Ranolazine
Placebo
Conditions
Locations
University of California, San Francisco
San Francisco, California 94143
United States
Mayo Clinic Florida
Jacksonville, Florida 32224
United States
University of Kansas Medical Center
Fairway, Kansas 66205
United States
University of Kansas Medical Center: Wichita
Wichita, Kansas 67214
United States
University of Missouri Health Care
Columbia, Missouri 65212
United States
The Ohio State University
Columbus, Ohio 43210
United States