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Completed Phase 3 Interventional

Trial to Evaluate Efficacy and Safety of Apraglutide in SBS-IF

ClinicalTrials.gov ID: NCT04627025

Public ClinicalTrials.gov record NCT04627025. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 7:12 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Double-blind, Randomized, Placebo-controlled Trial to Evaluate the Efficacy and Safety of Apraglutide in Adult Subjects With Short Bowel Syndrome and Intestinal Failure (SBS-IF)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of the trial is the confirmation of the efficacy of apraglutide to evaluate the efficacy of weekly subcutaneous apraglutide in reducing parenteral support dependency.

Study identification

NCT ID
NCT04627025
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
VectivBio AG
Industry
Enrollment
164 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 26, 2021 (Actual)
Primary completion
Jan 2, 2024 (Actual)
Completion
Feb 22, 2024 (Actual)
Last update posted
Nov 27, 2024

2021 – 2024

United States locations

U.S. sites
13
U.S. states
12
U.S. cities
13
Facility City State ZIP Site status
Ronald Reagan UCLA Medical Center Los Angeles California 90095 —
Gastroenterology Group of Naples Naples Florida 34102 —
Northwestern University Chicago Illinois 60611 —
Henry Ford Medical Center - Columbus Novi Michigan 48377 —
Mayo Clinic Rochester Minnesota 55905 —
University of Nebraska Medical Center Omaha Nebraska 68198 —
Mount Sinai Medical Center New York New York 10029 —
Duke University Hospital Durham North Carolina 27705 —
Cincinnati Children's Hospital Medical Center Cincinnati Ohio 45229-3039 —
Cleveland Clinic Foundation Cleveland Ohio 44195 —
Hospital of the University of Pennsylvania Philadelphia Pennsylvania 19104 —
Vanderbilt University Medical Center, Center for Human Nutrition Nashville Tennessee 37212 —
University of Washington Medical Center Seattle Washington 98195 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 55 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04627025, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 27, 2024 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04627025 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →