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Completed Phase 2 Interventional

GV101 in Healthy Obese Participants

ClinicalTrials.gov ID: NCT06979505

Public ClinicalTrials.gov record NCT06979505. 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 Sep 26, 2026, 10:10 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

Dose-ranging Double-blind, Placebo-controlled Phase 2 Trial of GV101 for Weight Loss in Healthy Obese Participants

Brief summary

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

The purpose of this trial is to evaluate the efficacy and safety of GV101 for weight loss over a range of doses in participants with obesity. The primary efficacy endpoint is the mean percent change in body weight from baseline at Week 16 in each treated group as compared with placebo.

Study identification

NCT ID
NCT06979505
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Graviton Bioscience Corporation
Industry
Enrollment
131 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 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 29, 2025
Primary completion
Jan 27, 2026
Completion
Jan 27, 2026
Last update posted
Feb 3, 2026

2025 – 2026

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Lakeview Clinical Research, LLC Guntersville Alabama 35976 —
Arizona Clinical Trials Tucson Arizona 85712 —
Catalina Research Institute, LLC Montclair California 91763 —
Encompass Clinical Research Spring Valley California 91978 —
Louisville Metabolic and Atherosclerosis Research Center (L-MARC) Louisville Kentucky 40213 —
Tandem Clinical Research Marrero Louisiana 70072 —
Study Metrix Research City of Saint Peters Missouri 63303 —
Kansas City Research Institute Kansas City Missouri 64131 —
Mercury Street Medical Butte Montana 59701 —
Hassman Research Institute Berlin New Jersey 08009 —
Coastal Research Institute, LLC Fayetteville North Carolina 28304 —
Lillestol Research, LLC Fargo North Dakota 58104 —
Velocity Clinical Research - Cleveland Cleveland Ohio 44122 —
Velocity Clinical Research - Dallas Dallas Texas 75230 —
Advanced Research Institute - Ogden Ogden Utah 84405 —
Chrysalis Clinical Research St. George Utah 84790 —

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06979505, 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 Feb 3, 2026 · Synced Sep 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06979505 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →