Assessment of KAN-101 in Celiac Disease (ACeD)
Sponsored by Kanyos Bio, Inc., a wholly-owned subsidiary of Anokion SA
About this trial
Last updated 4 years ago
Study ID
Status
Type
Phase
Placebo
Accepting
Not accepting
Trial Timing
Ended 4 years ago
What is this trial about?
What are the Participation Requirements?
Key Inclusion Criteria:
1. Adults aged 18 to 70 years inclusive
2. Diagnosed with celiac disease based on positive serology (eg, tissue transglutaminase
IgA antibody and/or deamidated gliadin peptide IgG) and intestinal histology
consistent with ≥ Marsh Type II or with evidence of villous atrophy
3. Has HLA-DQ2.5 genotype (HLA-DQA1*05 and HLA-DQB1*02) (homozygotes or heterozygotes)
4. Has followed a GFD for > 12 months immediately prior to study entry
5. Negative or weak positive for tTG-IgA and negative or weak positive for DGP-IgA/IgG
during screening
6. Male or female. Females of childbearing potential must use at least 2 acceptable birth
control methods
7. Capable of understanding and complying with protocol requirements
8. Patient understands and has signed the informed consent form
Key Exclusion Criteria:
1. Refractory celiac disease
2. Selective IgA deficiency
3. Positive for HLA-DQ8 (DQA1*03, DQB1*0302)
4. Previous treatment with tolerance-inducing therapies for celiac disease
5. Known wheat allergy
6. Part B only: History of hyperacute or prolonged symptoms following gluten exposure
7. Uncontrolled or significant medical conditions (including active infections or chronic
hepatitis) which, in the opinion of the Investigator, preclude participation
8. History of dermatitis herpetiformis
9. Pregnant or breastfeeding