About this trial
A study to discover if ZED1227 can improve continued celiac disease symptoms despite a gluten-free diet
Eligibility criteria
Qualifiers
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
Disqualifiers
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
Trial design
Treatments tested in this trial
- ZED1227 + SIGE
- Placebo
Treatment groups
Sponsors and collaborators
Dr. Falk Pharma GmbH
Lead sponsor
Takeda Development Center Americas, Inc.
Collaborator