About this trial
A study to discover if ZED1227 can improve continued celiac disease symptoms despite a gluten-free diet
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Parallel
Treatments tested in this trial
ZED1227 + SIGE
Drugoral treatment with different daily doses of ZED1227 vs placebo
Placebo
Other interventionPlacebo + SIGE
Treatment groups
Trial outcomes
Primary outcomes
Change in CDSD GI Specific Symptom Score
Secondary outcomes
Change in PRO: Change from baseline in the percentage of Symptom Free Days (SFD)
Histological assessment of villous height to crypt depth ratio (VH:CrD)
Change in CDSD Non-Stool GI Symptom Score (abdominal pain, bloating, nausea)
Proportion of subjects with histologic non-worsening, defined as change in VH:CrD ≥ 0
Sponsors and contacts
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Dr. Falk Pharma GmbH
Lead sponsor
Takeda Development Center Americas, Inc.
Collaborator