Evaluating The Efficacy And Tolerability Of ZED1227 In Subjects With Non-responsive Celiac Disease

Overview

About this study

A study to discover if ZED1227 can improve continued celiac disease symptoms despite a gluten-free diet

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

* Signed informed consent
* Men or women between 18 and 80 years of age, inclusively
* Documented initial biopsy-proven diagnosis of celiac disease or, in case of missing histological documentation, TG2-IgA > 10 x upper limit of normal (ULN) at diagnosis at least 12 months prior to V0
* Adherence to a gluten-free diet (GFD) for at least 12 months prior to V0
* Human leukocyte antigen DQ (HLA-DQ) typing compatible with celiac disease

Exclusion Criteria:

* Presence of hypo- or hyperthyroidism. A patient with a well-controlled thyroid disorder during the previous 3 months can be included
* Patients diagnosed to have confirmed refractory celiac disease type I (RCDI) or II (RCDII), with the exception that patients with a diagnosis of RCDI can be considered for inclusion if they do not have clear signs of T cell monoclonality or atypical T cells (e.g., as revealed by CD3/CD8 immunohistochemistry) and if they do not present with very severe symptoms and/or parameters of significant malabsorption and if they have not received prior treatment with immunosuppressants such as budesonide or azathioprine,
* Severe complications of celiac disease
* Concomitant diseases of the intestinal tract in addition to celiac disease, such as Crohn's disease, ulcerative colitis, other forms of inflammatory bowel disease, severe irritable bowel syndrome, microscopic colitis, small intestinal bacterial overgrowth (SIBO), exocrine pancreatic insufficiency; any other active diseases of the intestinal tract (e.g., active, untreated peptic ulcer, esophagitis, gastroesophageal reflux disease) that might, in the investigator's opinion, interfere with assessment of symptoms of abdominal pain, diarrhoea, or other components of celiac disease
* History or presence of dermatitis herpetiformis

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 03/16/2026. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

Contact us for the latest status

Contact information:

Clinical Studies Unit - Arizona

(480) 301-8000

ARZCSUADMIN@mayo.edu

Rochester, Minn.

Mayo Clinic principal investigator

Adam Bledsoe, M.D.

Contact us for the latest status

Contact information:

Chadrick Hinson

5072660237

hinson.chadrick@mayo.edu

More information

Publications

Publications are currently not available