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.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Frequency of Treatment-Emergent Adverse Events
Timeframe: Up to 28 weeks
Tolerability of treatment assignment
Timeframe: Up to 28 weeks
Muscle cramp frequency
Timeframe: Up to 28 weeks
Muscle cramp severity
Timeframe: Up to 28 weeks
Muscle cramps impact on quality of life
Timeframe: Up to 28 weeks
Safety Lab Cystatin C
Timeframe: Up to 28 weeks
Safety Lab Estimated Glomerular Filtration Rate (eGFR)
Timeframe: Up to 28 weeks
Safety Lab Alanine Transaminase (ALT)
Timeframe: Up to 28 weeks
Safety Lab Aspartate Transferase (AST)
Timeframe: Up to 28 weeks
Safety Lab Alkaline Phosphatase (ALP)
Timeframe: Up to 28 weeks
Safety Lab Total Bilirubin
Timeframe: Up to 28 weeks