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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 Jul 22, 2026, 4:55 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, Parallel Arm, Multiple-Dose Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of BMS-646256 in Obese and High Risk Overweight Subjects

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

  • BMS-646256 Drug
  • Placebo Drug

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
Oct 31, 2006
Primary completion
Aug 31, 2007
Completion
Mar 31, 2009
Last update posted
Sep 16, 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 16, 2010 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00388609 live on ClinicalTrials.gov.

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