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Indole-3-PROpionic Acid Clinical Trials - Multiple Sclerosis (iPROACT-MS)

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• 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

• Deemed physically and mentally able to participate in this study

Locations
Other Locations
Denmark
Glostrup Hospital
RECRUITING
Glostrup Municipality
Contact Information
Primary
Jette Lautrup Frederiksen, MD, dr.med, professor
jette.lautrup.battistini@regionh.dk
+4538633041
Backup
Moschoula Passali, MSc, PhD
moschoula.passali@regionh.dk
+45 38633467
Time Frame
Start Date: 2026-01-26
Estimated Completion Date: 2028-07-15
Participants
Target number of participants: 220
Treatments
Placebo_comparator: Placebo
Placebo capsules
Experimental: Indole-3-propionic acid (IPA)
IPA capsules
Related Therapeutic Areas
Sponsors
Collaborators: University of Copenhagen, University of Southampton
Leads: Glostrup University Hospital, Copenhagen

This content was sourced from clinicaltrials.gov