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Terminated Phase 2 Interventional

Multiple-dose Study to Evaluate the Efficacy, Safety and Pharmacokinetics of BMS-646256 in Obese Subjects

ClinicalTrials.gov ID: NCT00388609

Public ClinicalTrials.gov record NCT00388609. 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 Nov 9, 2026, 9:54 PM EST

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Official title

A Randomized, Double-blind, Placebo-Controlled, Parallel Arm, Multiple-Dose Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of BMS-646256 in Obese and High Risk Overweight Subjects

Brief summary

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

The purpose of this study is to learn if BMS-646256 can cause weight loss in men and women who are: * overweight with high blood pressure or high cholesterol or * obese The safety of this treatment will also be studied

Study identification

NCT ID
NCT00388609
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
705 participants

Conditions and interventions

Conditions

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
Nov 2006 (Type not available)
Primary completion
Sep 2007 (Actual)
Completion
Apr 2009 (Actual)
Last update posted
Sep 17, 2010

2006 – 2009

United States locations

U.S. sites
10
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
Ucla Center For Human Nutrition Los Angeles California 90095 —
Domenica M. Rubino, Md Washington D.C. District of Columbia 20037 —
Csra Partners In Health, Inc Augusta Georgia 30909 —
Springfield Diabetes And Endocrine Center Springfield Illinois 62704 —
Pennington Biomedical Research Center Baton Rouge Louisiana 70808 —
The Center For Nutrition & Preventive Medicine, Pllc Charlotte North Carolina 28211 —
Duke University Medical Center Durham North Carolina 27710 —
Medical University Of South Carolina Charleston South Carolina 29425 —
Hampton Roads Center For Clinical Research Inc. Norfolk Virginia 23502 —
National Clinical Research, Inc. Richmond Virginia 23294 —

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 NCT00388609, 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 Sep 17, 2010 · Synced Nov 9, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00388609 live on ClinicalTrials.gov.

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