RecruitingPhase 2NCT07298343

Evaluating the Efficacy and Tolerability of ZED1227 in Subjects With Non-responsive Celiac Disease

A Phase II, Double-blind, Randomised, Placebo-controlled Trial to Evaluate the Efficacy and Tolerability of ZED1227 in Celiac Disease Subjects Experiencing Symptoms Despite Gluten-free Diet


Sponsor

Dr. Falk Pharma GmbH

Enrollment

356 participants

Start Date

Jun 10, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

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


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria5

  • 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 Criteria5

  • 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

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGZED1227 + SIGE

oral treatment with different daily doses of ZED1227 vs placebo

OTHERPlacebo

Placebo + SIGE


Locations(1)

University Medical Center Mainz

Mainz, Germany

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07298343


Related Trials