🏛️ Verified NIH Record • Updated 2026-08-11

Efficacy And Safety Evaluation of Glepaglutide in Treatment of SBS (NCT07197944)

A Phase 3, Double-blind, Randomized, Parallel Group, Placebo-controlled, Multicenter Trial to Confirm the Efficacy and Safety of Glepaglutide 10 mg Twice Weekly, Followed by a Long-term, Open-label Safety Evaluation in Patients With Short Bowel Syndrome-intestinal Failure (SBS-IF)

🟢 Recruiting Phase3 💊 Investigational Drug / Biologic Sponsor: Zealand Pharma

🩺 Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: The University of Chicago Medicine — Chicago, Illinois

Age range: 18 Years to 90 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (31 Sites)

Showing the first 25 of 31 sites.

  • The University of Chicago Medicine — Chicago, Illinois
  • Washington University Center for Advanced Medicine — St Louis, Missouri
  • Lied Transplant Center at Nebraska Medical Center — Omaha, Nebraska
  • New York Presbyterian Hospital-Columbia University Medical Center — New York, New York
  • Vanderbilt University Medical Center — Nashville, Tennessee
  • Universitätsklinikum AKH Wien — Vienna, State of Vienna
  • Universitair Ziekenhuis (UZ) Leuven — Leuven,
  • Rigshospitalet-Blegdamsvej 9 — Copenhagen,
  • Helsingin Yliopistollinen Keskussairaala — Helsinki,
  • AP-HP - Hôpital Beaujon — Clichy,
  • Universitätsmedizin Rostock — Rostock, Mecklenburg-Vorpommern
  • Eugastro Klinische Studien GmbH — Leipzig, Saxony
  • Universitätsklinikum Aachen — Aachen,
  • Charité - Universitätsmedizin Berlin — Berlin,
  • Universitätsklinikum Bonn — Bonn,
  • Asklepios Klinik St. Georg — Hamburg,
  • Eszak-Pesti Centrumkorhaz -Honvedkorhaz- Podmaniczky utcai telephely — Budapest,
  • Semmelweis Egyetem - Sebészeti, Transzplantációs és Gasztroenterológiai Klinika — Budapest,
  • Dél-budai Centrumkórház Szent Imre Egyetemi Oktatókórház — Budapest,
  • Fondazione Policlinico Universitario A. Gemelli IRCCS - PPDS — Rome, Lazio
  • Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico — Milan,
  • Azienda Ospedale - Università Padova — Padova,
  • Radboud Universitair Medisch Centrum — Nijmegen, Gelderland
  • Oslo Universitetssykehus HF, Ullevål — Oslo,
  • Wojewodzki Specjalistyczny Szpital im. M. Pirogowa w Lodzi — Lodz, Lódzkie

📞 Contact the Study Coordinator

Phone: (773) 702-6921

Email: csemrad@medicine.bsd.uchicago.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗