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A Trial to Assess the Efficacy and Safety of TEV-53408 in Adults With Celiac Disease

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Condition(s):
Celiac Disease
Status:
Recruiting
Requirements:
18 Years to 64 Years
Interventions:
Drug: TEV-53408, Placebo
Learn more Primary objectives: The primary efficacy objective of the trial is to assess the ability of TEV-53408 to attenuate gluten-induced enteropathy in adults with celiac disease. The primary safety objective of the trial is to assess the safety of TEV-53408 in adults with celiac disease. Secondary objective:A secondary objective is to further assess the efficacy of TEV-53408 in adults with celiac disease.The expected trial duration per participant is approximately 86 weeks.