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NCT04627025 · ClinicalTrials.gov registry record · Phase 3

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

A Phase 3 study of Short Bowel Syndrome, sponsored by VectivBio.

Completed
Registry status
Phase 3
Development phase
164
Enrollment target
20
Study locations

NCT04627025 is a Phase 3 study of Short Bowel Syndrome that has completed, run by VectivBio. The registered enrollment target is 164 participants, roughly in line with the 175-participant average among 17 other Short Bowel Syndrome trials with a reported enrollment target. The trial reports 20 study locations across 14 states.

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The verdict

NCT04627025, a Phase 3 study of Short Bowel Syndrome, has completed, sponsored by VectivBio.

COMPLETED
Registry status
Phase 3
Development phase
164 participants
Enrollment target
20
Study locations

Study Summary

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.

Conditions Studied

Interventions

  • DRUG apraglutide

Study Locations (20)

Other

  • University Hospital Foundation Favaloro - Buenos Aires
  • University Hospital Brussels - Brussels
  • University Hospital Brno - Brno
  • University Hospital Hradec Kralove - Hradec Králové
  • Hospital Novy Jicin - Nový Jičín
  • University Hospital Plzen - Pilsen

Ohio

  • Cincinnati Children's Hospital Medical Center - Cincinnati
  • Cleveland Clinic Foundation - Cleveland

California

  • Ronald Reagan UCLA Medical Center - Los Angeles

Florida

  • Gastroenterology Group of Naples - Naples

Illinois

  • Northwestern University - Chicago

Michigan

  • Henry Ford Medical Center - Columbus - Novi

Minnesota

  • Mayo Clinic - Rochester

Nebraska

  • University of Nebraska Medical Center - Omaha

Trial Details

FieldValue
Enrollment Target 164 participants
Start Date 2021-01-26
Est. Completion 2024-02-22
Phase Phase 3

Sponsor

VectivBio

4 total trials

What the Registry Record Tells You About NCT04627025

The ClinicalTrials.gov registry entry for NCT04627025 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 164 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 175-participant average among 17 other Short Bowel Syndrome trials with a reported enrollment target. The listed sponsor is VectivBio, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Short Bowel Syndrome appearing as the primary indexed condition, and to 1 intervention - of which apraglutide is the first listed.

NCT04627025 reports 20 study locations spanning 14 distinct geographic areas - top geographies include Other, Ohio, California.

Frequently Asked Questions

What is clinical trial NCT04627025 about?

NCT04627025 is a clinical study titled "Trial to Evaluate Efficacy and Safety of Apraglutide in SBS-IF". 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.

What is the current status of trial NCT04627025?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 164 participants. The study started on 2021-01-26. Estimated completion is 2024-02-22.

What conditions does trial NCT04627025 study?

This clinical trial studies the following conditions: Short Bowel Syndrome.

What interventions are being tested in trial NCT04627025?

The interventions under investigation include: apraglutide (DRUG).

Who is sponsoring clinical trial NCT04627025?

This trial is sponsored by VectivBio, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04627025 being conducted?

This trial has 20 study locations across California, Florida, Illinois, Michigan, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Short Bowel Syndrome

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.