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Clinical Trial Summary

This study has 3 treatment phases, a 12-Week Induction Phase, a 40-Week Maintenance Phase, and a 48-Week Extension Phase. The objective is to evaluate the efficacy and safety of obefazimod compared to placebo as induction and maintenance therapy in subjects with moderately to severely active CD after inadequate response (no response, loss of response, or intolerance) to conventional therapies and/or advanced therapies. The primary objective for the 48-Week Extension Phase is to evaluate the safety and tolerability of obefazimod compared with placebo in subjects who are enrolled in the Extension Phase.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT06456593
Study type Interventional
Source Abivax S.A.
Contact Laurence Desroys du Roure, Pharm.D
Phone +33 6 3003 1132
Email laurence.desroysduroure@abivax.com
Status Not yet recruiting
Phase Phase 2
Start date September 2024
Completion date April 2028