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A Study of Efficacy, Safety, and Tolerability of KAN-101 in People With Celiac Disease — SynCeD  

Celiac Disease Clinical Trial

Official title:
A Phase 2a Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of KAN-101 In Participants With Celiac Disease

Clinical Trial Summary

The study goal is to evaluate the efficacy, safety, and tolerability of KAN-101 in participants with Celiac Disease (CeD)

Clinical Trial 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. Up to 52 participants who meet study inclusion/exclusion criteria will be randomized 1:1 to receive KAN-101 or placebo. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06001177
Study type Interventional
Source Anokion SA
Contact Kanyos Bio, Inc (a wholly owned subsidiary of Anokion SA)
Phone +1 857-320-6607
Email clinicaltrials@anokion.com
Status Recruiting
Phase Phase 2
Start date December 13, 2023
Completion date June 2025
View Details
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