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Evaluation of Long Term Safety and Efficacy of Glepaglutide in Treatment of SBS
NCT03905707 · View on ClinicalTrials.gov ↗
Study Summary
The primary objective of the trial is to evaluate the long-term safety of glepaglutide treatment in patients with short bowel syndrome (SBS). Glepaglutide is the International Nonproprietary Name and USAN for ZP1848.
Conditions Studied
Interventions
- DRUG glepaglutide
Study Locations (20)
Other
- UZ Leuven — Leuven
- The Royal Alexandra Hospital — Edmonton
- Western University — London
- University Health Network - Toronto General Hospital — Toronto
- Rigshospitalet — Copenhagen
- Hôpital Beaujon — Clichy
- Centre Hospitalier Lyon-Sud — Pierre-Bénite
- Charité - Universitätsmedizin Berlin — Berlin
- Universitätsklinikum Bonn — Bonn
- Universitätsklinikum Frankfurt - Med. Klinik I — Frankfurt
- Asklepios Kliniken Hamburg GmbH — Hamburg
- Universitätsmedizin Rostock — Rostock
- UMC Radboud Nijmegen — Nijmegen
District of Columbia
- Georgetown University Medical Center — Washington D.C.
Illinois
- University of Chicago Children's Hospital — Chicago
Minnesota
- Mayo Clinic College of Medicine — Rochester
Nebraska
- University of Nebraska Medical Center — Omaha
New York
- Mount Sinai Hospital — New York
Ohio
- Cleveland Clinic — Cleveland
Tennessee
- Vanderbilt University Medical Center, Nashville — Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 145 participants |
| Start Date | 2019-05-07 |
| Est. Completion | 2026-04 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03905707
The ClinicalTrials.gov registry entry for NCT03905707 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 145 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Zealand Pharma, which has 8 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Short Bowel Syndrome appearing as the primary indexed condition, and to 1 intervention — of which glepaglutide is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03905707 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Other, District of Columbia, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03905707 about?
NCT03905707 is a clinical study titled "Evaluation of Long Term Safety and Efficacy of Glepaglutide in Treatment of SBS". The primary objective of the trial is to evaluate the long-term safety of glepaglutide treatment in patients with short bowel syndrome (SBS). Glepaglutide is the International Nonproprietary Name and USAN for ZP1848.
What is the current status of trial NCT03905707?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 145 participants. The study started on 2019-05-07. Estimated completion is 2026-04.
What conditions does trial NCT03905707 study?
This clinical trial studies the following conditions: Short Bowel Syndrome. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03905707?
The interventions under investigation include: glepaglutide (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03905707?
This trial is sponsored by Zealand Pharma, which has 8 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03905707 being conducted?
This trial has 20 study locations across District of Columbia, Illinois, Minnesota, Nebraska, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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