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Terminated Phase 2 Interventional

VIBRANT Study of Vurolenatide in Adult Patients With Short Bowel Syndrome.

ClinicalTrials.gov ID: NCT04988997

Public ClinicalTrials.gov record NCT04988997. 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 Jul 23, 2026, 3:36 AM 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 Phase 2, Double-Blind, Double-Dummy, Placebo-Controlled, Multicenter Study of the Efficacy, Safety, and Tolerability of Vurolenatide in Adult Patients With Short Bowel Syndrome

Study identification

NCT ID
NCT04988997
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
9 Meters Biopharma, Inc.
Industry
Enrollment
12 participants

Conditions and interventions

Interventions

  • Vurolenatide 50mg/PBO Drug
  • Vurolenatide 100mg/PBO Drug
  • Vurolenatide 50/50 mg Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Jun 13, 2021
Primary completion
Aug 4, 2022
Completion
Aug 23, 2022
Last update posted
Dec 19, 2022

2021 – 2022

United States locations

U.S. sites
6
U.S. states
6
U.S. cities
6
Facility City State ZIP Site status
Research Site Gainesville Florida 32610
Research Site Atlanta Georgia 30322
Research Site Boston Massachusetts 02118
Research Site Omaha Nebraska 68198
Research Site Durham North Carolina 27710
Research Site Nashville Tennessee 37212

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04988997, 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 Dec 19, 2022 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04988997 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →