Study of the Safety, Tolerability, Pharmacokinetics and Biomarker of DONQ52 in Celiac Disease Patients
Part of paid clinical trials in Anniston, Alabama.
- Sponsor
- Chugai Pharmaceutical
- Study ID
- NCT05425446
- Phase
- PHASE1
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- DONQ52 — DRUGSubcutaneous (SC) injection
- Placebo — DRUGSubcutaneous (SC) injection
Study Details
This study is to characterize the safety and tolerability of an investigational drug called DONQ52 and consists of a single ascending dose part (Part A) and a multiple ascending dose part (Part B) in well-controlled celiac disease patients.
Key Dates
- Start date
- Sep 19, 2022
- Status verified
- Jan 2025
- Primary completion
- Aug 9, 2024
- Completion
- Jan 17, 2025
Study Design
- Enrollment
- 56 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: SAD Cohort 1All randomized patients will receive one dose of either DONQ52 Dose A or placebo
- Experimental: SAD Cohort 2All randomized patients will receive one dose of either DONQ52 Dose B or placebo
- Experimental: SAD Cohort 3All randomized patients will receive one dose of either DONQ52 Dose C or placebo
- Experimental: SAD Cohort 4All randomized patients will receive one dose of either DONQ52 Dose D or placebo
- Experimental: MAD Cohort 1All randomized patients will receive multiple dose of either DONQ52 Dose E or placebo
- Experimental: MAD Cohort 2All randomized patients will receive multiple dose of either DONQ52 Dose F or placebo
- Experimental: MAD Cohort 3All randomized patients will receive multiple dose of either DONQ52 Dose G or placebo
Primary Outcome Measure
Incidence and severity of treatment-emergent adverse events (TEAEs) as assessed by the Common Terminology Criteria for Adverse Events (CTCAE) v5.0 or higher [ Time Frame: Up to 246 days ]
Locations (18)
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