Indole-3-PROpionic Acid Clinical Trials - Multiple Sclerosis

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorGlostrup University Hospital, Copenhagen

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

220 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Glostrup University Hospital, Copenhagen

Lead sponsor

University of Copenhagen

Collaborator

University of Southampton

Collaborator