A Six Week Efficacy Safety and Tolerability Study of V565 in Crohn's Disease

  • STATUS
    Not Recruiting
  • participants needed
    126
  • sponsor
    VHsquared Ltd.
Updated on 22 January 2021

Summary

The purpose of this study is to evaluate the efficacy and safety of V565 in participants with active Crohn's Disease.

Description

This study will be a multiple-site, double-blind, placebo-controlled, parallel-group study in approximately 126 subjects with a confirmed diagnosis of CD for at least three months and have CD involving the ileum and/or colon. Following a screening period of up to 28 days, subjects will be randomly allocated into one of two treatment arms: either V565 or placebo using a 2:1 active:placebo ratio for a treatment period of 6 weeks.

Subjects will be treated with study drug as an add-on to any permitted stable medications already being taken for CD.

Details
Condition Crohn's Disease
Treatment Placebo, V565
Clinical Study IdentifierNCT02976129
SponsorVHsquared Ltd.
Last Modified on22 January 2021

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