Safety and Efficacy Study of BMS-823778 to Treat Uncontrolled High Blood Pressure in Overweight and Obese Patients

September 23, 2015 updated by: Bristol-Myers Squibb

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Phase 2B Trial to Evaluate the Safety and Efficacy of BMS-823778 in Overweight and Obese Subjects With Inadequately Controlled Hypertension

The purpose of this study is to determine whether BMS-823778 is safe and effective in the treatment of hypertension in overweight and obese patients.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Terminated

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
7

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Colombia
      • Barranquilla, Colombia
        • Local Institution
      • Bucaramanga, Colombia
        • Local Institution
      • Cartagena, Colombia
        • Local Institution
      • Manizales, Colombia
        • Local Institution
      • Medellin, Colombia
        • Local Institution
  • Hungary
      • Balatonfured, Hungary, H-8230
        • Local Institution
      • Budapest, Hungary, 1125
        • Local Institution
      • Budapest, Hungary, 1134
        • Local Institution
      • Budapest, Hungary, 1133
        • Local Institution
      • Debrecen, Hungary, 4026
        • Local Institution
  • Puerto Rico
      • Ponce, Puerto Rico, 00717
        • Local Institution
  • Sweden
      • Odeshog, Sweden, 599 31
        • Local Institution
      • Stockholm, Sweden, 141 86
        • Local Institution
  • United States
    • Arkansas
      • Jonesboro, Arkansas, United States, 72401
        • NEA Baptist Clinic
    • California
      • Los Angeles, California, United States, 90057
        • Local Institution
      • Palm Springs, California, United States, 92262
        • Desert Medical Group Inc.
    • Florida
      • Coral Gables, Florida, United States, 33134
        • Local Institution
    • Georgia
      • Atlanta, Georgia, United States, 30303
        • Local Institution
    • Louisiana
      • Baton Rouge, Louisiana, United States, 70808-4124
        • Pennington Biomedical Research Center
      • New Orleans, Louisiana, United States, 70115
        • Local Institution
    • New Jersey
      • Edison, New Jersey, United States, 08817
        • Anderson and Collins Clinical Research, Inc.
      • Trenton, New Jersey, United States, 08611
        • Premier Research
    • New York
      • Syracuse, New York, United States, 13202-3108
        • Syracuse Preventive Cardiology
    • North Carolina
      • Charlotte, North Carolina, United States, 28204
        • Metrolina Internal Medicine
      • Greensboro, North Carolina, United States, 27408
        • PharmQuest, LLC
      • Salisbury, North Carolina, United States, 28144
        • PMG Research of Salisbury
      • Shelby, North Carolina, United States, 28150
        • Local Institution
      • Shelby, North Carolina, United States, 28152
        • Local Institution
      • Winston-salem, North Carolina, United States, 27103
        • Local Institution
    • Ohio
      • Cincinnati, Ohio, United States, 45246
        • Sterling Research Grp, Ltd.
    • South Carolina
      • Greenville, South Carolina, United States, 29615
        • Local Institution
    • Utah
      • Layton, Utah, United States, 84041
        • Local Institution
    • Virginia
      • Manassas, Virginia, United States, 20110
        • Manassas Clinical Research Center
      • Norfolk, Virginia, United States, 23502
        • National Clinical Research - Norfolk, Inc.
      • Richmond, Virginia, United States, 23294
        • National Clinical Research - Richmond, Inc.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

18 years to 80 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Qualifying seated blood pressure between ≥90 and ≤105 mmHg diastolic AND ≤155 mmHg systolic
  • Mean 24-hour diastolic blood pressure ≥85 mmHg
  • Body mass index (BMI) ≥27 kg/m2
  • If receiving an oral anti-hyperglycemic medication or a cholesterol lowering medication, receiving a stable dose for at least 6 weeks

Exclusion Criteria:

  • History of Cushing's disease or syndrome, or Addison's disease
  • Glycosylated hemoglobin (HbA1c) ≥10%
  • Cerebrovascular insult, unstable angina, or myocardial infarction (MI) within 6 months
  • History of impaired renal or hepatic function
  • BMI ≥50 kg/m2
  • Any injectable antihyperglycemic agent (such as insulin) within 16 weeks
  • Currently receiving more than one class of antihypertensive agents within 4 weeks
  • Daily use of nonsteroidal anti-inflammatory agents within 1 week
  • Use of androgen medications, including topical preparations, within 6 weeks
  • Diagnosis or history of breast cancer

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: QUADRUPLE

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
EXPERIMENTAL: Arm 1: BMS-823778 (2mg)
Drug: BMS-823778
Capsules, Oral, 2 mg, Once daily, 12 weeks
Drug: BMS-823778
Capsules, Oral, 6 mg, Once daily, 12 weeks
Drug: BMS-823778
Capsules, Oral, 15 mg, Once daily, 12 weeks
EXPERIMENTAL: Arm2: BMS-823778 (6mg)
Drug: BMS-823778
Capsules, Oral, 2 mg, Once daily, 12 weeks
Drug: BMS-823778
Capsules, Oral, 6 mg, Once daily, 12 weeks
Drug: BMS-823778
Capsules, Oral, 15 mg, Once daily, 12 weeks
EXPERIMENTAL: Arm 3: BMS-823778 (15mg)
Drug: BMS-823778
Capsules, Oral, 2 mg, Once daily, 12 weeks
Drug: BMS-823778
Capsules, Oral, 6 mg, Once daily, 12 weeks
Drug: BMS-823778
Capsules, Oral, 15 mg, Once daily, 12 weeks
EXPERIMENTAL: Arm4: Placebo
Drug: Placebo matching with BMS-823778
Capsules, Oral, 0 mg, Once daily, 12 weeks

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Time Frame
The dose-dependent trend among doses of BMS-823778 and placebo by assessing the change from baseline in 24-hour ambulatory diastolic blood pressure following 12 weeks of double-blind treatment
Time Frame: At Day -7 (baseline) and Week 12
At Day -7 (baseline) and Week 12

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Time Frame
Change in 24-hour ambulatory systolic blood pressure (SBP)(evaluation of the dose-dependent trend)
Time Frame: At Day -7 (baseline) and Week 12
At Day -7 (baseline) and Week 12
Change in 24-hour ambulatory diastolic blood pressure (DBP)
Time Frame: At Day -7 (baseline) and Week 12
At Day -7 (baseline) and Week 12
Change in 24-hour ambulatory SBP
Time Frame: At Day -7 (baseline) and Week 12
At Day -7 (baseline) and Week 12
Change in ambulatory daytime and nighttime DBP
Time Frame: At Day -7 (baseline) and Week 12
At Day -7 (baseline) and Week 12
Change in ambulatory daytime and nighttime SBP
Time Frame: At Day -7 (baseline) and Week 12
At Day -7 (baseline) and Week 12
Change in seated DBP
Time Frame: At Day -7 (baseline) and Week 12
At Day -7 (baseline) and Week 12
Change in seated SBP
Time Frame: At Day -7 (baseline) and Week 12
At Day -7 (baseline) and Week 12

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Bristol-Myers Squibb

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
July 1, 2012

Primary Completion (ACTUAL)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
November 1, 2012

Study Completion (ACTUAL)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
November 1, 2012

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
May 17, 2012

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
May 18, 2012

First Posted (ESTIMATE)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
May 21, 2012

Study Record Updates

Last Update Posted (ESTIMATE)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
October 12, 2015

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
September 23, 2015

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
September 1, 2015

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • MB121-008
  • 2012-000509-54 (EUDRACT_NUMBER)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Cookie Settings

We use cookies to ensure that we give you the best experience on our website. For more details carefully read our Privacy and Cookies Policy. ...>>>You can change your preferences or withdraw your consent at any time by deleting the cookies from your website or computer as described in the policy. Please accept it and choose your preferences by ticking the corresponding boxes in the "Manage Settings" section below. Please carefully read our Terms of Service before you proceed with using any part of this website.
«Manage Settings