A Multicenter, Multinational, Randomized, Double-blind, Placebo-controlled Phase 3, Induction Study to Evaluate the Efficacy and Safety of Duvakitug in Participants With Moderately to Severely Active Crohn's Disease
A Multicenter, Multinational, Randomized, Double-blind, Placebo-controlled Phase 3, Induction Study to Evaluate the Efficacy and Safety of Duvakitug in Participants With Moderately to Severely Active Crohn's Disease
This is a multinational, multicenter, randomized, double-blind, placebo-controlled, Phase 3 induction study, comprised of 3 sub-studies, to evaluate the efficacy and safety of duvakitug in participants with moderately to severely active CD. Study details include:
The study duration may be up to 35 weeks with:
The number of scheduled study visits for participants who continue to the Pivotal Maintenance Study (EFC18327) will be up to 8 (Sub-Study 1 and Sub-Study 2) and up to 15 for participants who enroll in Sub-Study 3.
Inclusion Criteria:
Exclusion Criteria:
The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.
Contact-US@sanofi.com800-633-1610 ext. option 6
Scottsdale, Arizona 85258, United States
Canoga Park, California 91304, United States
Coronado, California 92118-1408, United States
Rancho Cucamonga, California 91730, United States
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Gorna Oryahovitsa, Oblast Veliko Tirnovo 5100, Bulgaria
Ludwigshafen am Rhein, Rhineland-Palatinate 67067, Germany
Rozzano, 20089, Israel
Saga, 840-8571, Italy
Osaka, 540-0006, Japan
Sendai, 983-8520, Japan
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KwaZulu-Natal, 4449, South Africa
Changhua County, 500209, Taiwan