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Clinical Trial Summary

The purpose of this study is to assess the safety and efficacy of Nicotinamide riboside (NR) for treatment of patients with progressive multiple sclerosis. The main question it aims to answer is: • Does NR delay disability progression in progressive multiple sclerosis? Participants will be treated with NR or placebo for 30 months,


Clinical Trial Description

After being informed about the study and risks, all patients giving written informed consent will undergo a screening period to determine eligibility for study entry. At baseline patients who meet the eligibility requirements will be randomised in a double- blinded manner (patient and investigator) in a 1:1 ratio to nicotinamide riboside (1000 mg daily) or placebo (once a day) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05740722
Study type Interventional
Source Haukeland University Hospital
Contact Kjell-Morten Myhr
Phone +47 55976031
Email kjell-morten.myhr@helse-bergen.no
Status Recruiting
Phase Phase 2
Start date May 3, 2023
Completion date December 30, 2027

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