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

K

Kanyos Bio

Status and phase

Completed
Phase 2

Conditions

Coeliac Disease
Celiac Disease

Treatments

Drug: KAN-101
Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT06001177
KAN-101-03

Details and patient eligibility

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.

Enrollment

55 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Previous diagnosis of celiac disease based on histology and positive celiac serology
  • HLA-DQ2.5 genotype
  • Gluten-free diet for at least 12 months
  • Negative or weak positive for transglutaminase IgA and negative or weak positive for DGP-IgA/IgG during screening
  • Screening intestinal biopsy demonstrating Vh:Cd ratio of 2.3 or higher

Exclusion criteria

  • Refractory celiac disease
  • HLA-DQ8 genotype
  • Selective IgA deficiency
  • Diagnosis of type-I diabetes
  • Other Active gastrointestinal diseases
  • History of dermatitis herpetiformis

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

55 participants in 2 patient groups, including a placebo group

Group 1
Experimental group
Description:
All eligible participants will receive 3 intravenous (IV) infusions of KAN-101
Treatment:
Drug: KAN-101
Group 2
Placebo Comparator group
Description:
All eligible participants will receive 3 intravenous (IV) infusions of placebo
Treatment:
Drug: Placebo

Trial documents
2

Trial contacts and locations

29

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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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