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About
The study goal is to evaluate the efficacy, safety, and tolerability of KAN-101 in participants with Celiac Disease (CeD)
Full description
Study KAN-101-03 is a multi-center, double-blind, placebo-controlled Phase 2a study to examine whether KAN-101 confers protection from gluten exposure induced histological changes in the duodenum and to further evaluate the safety/tolerability of KAN-101 in adult participants (≥18 years) with CeD on a gluten free diet. Approximately 52 participants who meet study inclusion/exclusion criteria will be randomized 1:1 to receive KAN-101 or placebo.
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Interventional model
Masking
55 participants in 2 patient groups, including a placebo group
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Central trial contact
Kanyos Bio, Inc (a wholly owned subsidiary of Anokion SA)
Data sourced from clinicaltrials.gov
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