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Clinical Trial Summary

The overall objective of the RESTORATiVE303 study is to evaluate the safety and the Clostridioides difficile infection (CDI) recurrence rate at Week 8 in participants who receive a 14-day course of VE303 or matching placebo. The objectives and endpoints are identical for Stage 1 (recurrent CDI) and Stage 2 (high-risk primary CDI).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06237452
Study type Interventional
Source Vedanta Biosciences, Inc.
Contact Mary Garfield
Phone 857-706-1427
Email Consortium02-ctinquiries@vedantabio.com
Status Recruiting
Phase Phase 3
Start date May 20, 2024
Completion date October 2027

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