About this trial
This study, iPROACT-MS, is part of the iPROACT group of clinical trials aiming to investigate the effects of oral supplementation with indole-3-propionic acid (IPA) in humans. IPA is naturally produced as a gut bacterial metabolite with the amino acid tryptophan as substrate. The primary aim of iPROACT-MS is to investigate whether patients with relapsing-remitting multiple sclerosis (RRMS) can benefit from supplementation with IPA. The hypothesis is that supplementation with IPA will protect against MS-related disease activity, neurodegeneration and metabolic abnormalities. Secondary, iPROACT-MS aims at elucidating the complex relationships between lifestyle, gut microbial factors, inflammation, oxidative stress, metabolic health, MS disease severity and MS disease activity.
Eligibility criteria
Qualifiers
Women and men ≥18 and ≤65 years of age
Diagnosed with RRMS according to the 2017 McDonald criteria (or newer updates)
Routinely treated and monitored for MS
Speak and read Danish
Disqualifiers
Active malignancy
Diagnosis of Crohn's disease and ulcerative colitis
Other comorbidities deemed to be relevant
Haematopoietic stem cell transplantation
Trial design
Treatments tested in this trial
- Placebo
- Indole-3-propionic acid (IPA)
Treatment groups
Sponsors and collaborators
Glostrup University Hospital, Copenhagen
Lead sponsor
University of Copenhagen
Collaborator
University of Southampton
Collaborator