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Terminated Phase 2 Interventional

A Study of Weekly Oral Dose of Ecnoglutide (VRB-101) for Weight Maintenance in Participants Who Have Obesity or Overweight With Weight-Related Comorbidities

ClinicalTrials.gov ID: NCT07553299

Public ClinicalTrials.gov record NCT07553299. 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 22, 2026, 8:10 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 Randomized, Double-Blind, Placebo-Controlled Phase 2 Study to Identify the Optimal Weekly Oral Dose of Ecnoglutide (VRB-101) for Maintaining Body Weight in Participants With Obesity or Overweight Who Have Weight-Related Comorbidities

Brief summary

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

The purpose of this study is to identify the weekly oral dose of VRB-101 (oral ecnoglutide) that can effectively maintain body weight in participants with a history of obesity or overweight with weight-related comorbidities.

Study identification

NCT ID
NCT07553299
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Verdiva Bio Dev Limited
Industry
Enrollment
8 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 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 12, 2026 (Actual)
Primary completion
Sep 11, 2026 (Actual)
Completion
Sep 11, 2026 (Actual)
Last update posted
Oct 13, 2026

2026

United States locations

U.S. sites
20
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
Clinical Study Site 202 Cullman Alabama 35055 —
Clinical Study Site 203 Phoenix Arizona 85028 —
Clinical Study Site 212 Tempe Arizona 85281 —
Clinical Study Site 201 Little Rock Arkansas 72205 —
Clinical Study Site 214 Santa Maria California 93454 —
Clinical Study Site 216 Stamford Connecticut 06905 —
Clinical Study Site 204 Bradenton Florida 34209 —
Clinical Study Site 221 Orange City Florida 32763 —
Clinical Study Site 215 St. Petersburg Florida 33704 —
Clinical Study Site 219 Niles Illinois 60714 —
Clinical Study Site 213 El Dorado Kansas 67042 —
Clinical Study Site 210 Petal Mississippi 39465 —
Clinical Study Site 205 Buffalo New York 14217 —
Clinical Study Site 206 Lenoir North Carolina 28645 —
Clinical Study Site 220 Oklahoma City Oklahoma 73111 —
Clinical Study Site 209 Jackson Tennessee 38305 —
Clinical Study Site 217 Houston Texas 77008 —
Clinical Study Site 211 Houston Texas 77040 —
Clinical Study Site 218 Irving Texas 75063 —
Clinical Study Site 207 Richmond Virginia 23226 —

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 NCT07553299, 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 Oct 13, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07553299 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →