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Clinical Trial Summary

A Phase 2 study to evaluate the safety, efficacy, and microbiota changes of VE202 in patients with mild to moderate ulcerative colitis (UC).


Clinical Trial Description

A Phase 2 double-blind, placebo-controlled, randomized study to evaluate the safety, efficacy, and microbiota changes of VE202 in biologic-naïve patients with mild to moderate UC. In Parts 1 and 2 of the study, patients will receive VE202 or placebo for 8 weeks or 2 weeks. In Part 3, patients will be followed for safety for 1 year from the start of treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05370885
Study type Interventional
Source Vedanta Biosciences, Inc.
Contact Mary Garfield, MS
Phone 203.906.5693
Email Consortium02-ctinquiries@vedantabio.com
Status Recruiting
Phase Phase 2
Start date May 8, 2023
Completion date November 10, 2025

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