Efficacy And Safety Evaluation of Glepaglutide in Treatment of SBS
Part of paid clinical trials in St Louis, Missouri.
- Sponsor
- Zealand Pharma
- Study ID
- NCT07197944
- Phase
- PHASE3
- Status
- Recruiting
Conditions
- Short Bowel Syndrome
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 90 Years
- Healthy Volunteers
- Not accepted
Interventions
- Glepaglutide — DRUGSubcutaneous (SC) injections twice weekly
- Placebo — OTHERSC injections twice weekly
Study Details
The purpose of the present Phase 3 trial is to confirm the efficacy and safety of glepaglutide 10 mg twice weekly in a patient population with SBS-IF and generate additional long-term safety data. Glepaglutide is the International Nonproprietary Name and United States Adopted Name (USAN) for ZP1848.
Key Dates
- Start date
- Feb 11, 2026
- Status verified
- Apr 2026
- Primary completion
- Oct 23, 2028
- Completion
- Feb 28, 2032
Study Design
- Enrollment
- 90 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Glepaglutide Group
- Placebo Comparator: Placebo GroupPlacebo for glepaglutide
Primary Outcome Measure
Change in weekly Parenteral Support (PS) volume [ Time Frame: Baseline to Week 24 ]
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Washington University Center for Advanced Medicine | St Louis | Missouri | 63110 | |
| Lied Transplant Center at Nebraska Medical Center | Omaha | Nebraska | 68105 | |
| New York Presbyterian Hospital-Columbia University Medical Center | New York | New York | 10032 | |
| Vanderbilt University Medical Center | Nashville | Tennessee | 37232 |
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