drugset / Trial / NCT03423121

A Trial of Bile Acid Supplementation in Patients With Multiple Sclerosis

NCT03423121

Phase 1/2 Completed 59 enrolled Johns Hopkins University
RandomizedParallel-groupDouble-blindTreatment

Summary

This study aims to identify the safety and tolerability of bile acid supplementation in patients with progressive Multiple Sclerosis (MS). Participants will also be assessed for an impact of the bile acid on their immune system and gut microbiome. Half of the participants will receive the bile acid tauroursodeoxycholic acid (TUDCA) and half will receive placebo. The investigators believe participants who take TUDCA will have normalization of blood bile acid levels, a normalization of abnormal immune response and a normalization of the gut microbiome.

Timeline

Start
2018-06-19
Primary completion
2022-04-28
Completion
2022-07-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Taurursodiol Small molecule 1 g Oral