Cardiovascular Outcomes Study of Naltrexone SR/Bupropion SR in Overweight and Obese Subjects With Cardiovascular Risk Factors (The Light Study)
Primary Purpose
Obesity, Overweight
Status
Terminated
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
NB32
PBO
Weight Management Program
Sponsored by

About this trial
This is an interventional treatment trial for Obesity focused on measuring Body Weight, Bupropion, Cardiovascular Diseases, Diabetes Mellitus, Diabetes Mellitus, Type 2, Endocrine System Diseases, Glucose Metabolism Disorders, Heart Diseases, Metabolic Diseases, Narcotic Antagonists, Naltrexone, Nutrition Disorders, Obesity, Overnutrition, Overweight
Eligibility Criteria
Inclusion Criteria:
- ≥50 years of age (women) or ≥45 years of age (men)
- Body mass index (BMI) ≥27 kg/m2 and ≤50 kg/m2
- Waist circumference ≥88 cm (women) or ≥102 cm (men)
At increased risk of adverse cardiovascular outcomes:
Cardiovascular disease (confirmed diagnosis or at high likelihood of cardiovascular disease) with at least one of the following:
- History of documented myocardial infarction >3 months prior to screening
- History of coronary revascularization
- History of carotid or peripheral revascularization
- Angina with ischemic changes (resting ECG), ECG changes on a graded exercise test (GXT), or positive cardiac imaging study
- Ankle brachial index <0.9 (by simple palpation) within prior 2 years
- ≥50% stenosis of a coronary, carotid, or lower extremity artery within prior 2 years
AND/OR
Type 2 diabetes mellitus with at least 2 of the following:
- Hypertension (controlled with or without pharmacotherapy at <145/95 mm Hg)
- Dyslipidemia requiring pharmacotherapy
- Documented low HDL cholesterol (<50 mg/dL in women or <40 mg/dL in men) within prior 12 months
- Current tobacco smoker
Exclusion Criteria:
- Myocardial infarction within 3 months prior to screening
- Angina pectoris Grade III or IV as per the Canadian Cardiovascular Society grading scheme
- Clinical history of cerebrovascular disease (stroke)
- History of tachyarrhythmia other than sinus tachycardia
- Planned bariatric surgery, cardiac surgery, or coronary angioplasty
- History of seizures (including febrile seizures), cranial trauma, or other conditions that predispose the subject to seizures
- History of mania or current diagnosis of active psychosis, active bulimia or anorexia nervosa (binge eating disorder is not exclusionary)
- Any condition with life expectancy anticipated to be less than 4 years (e.g., congestive heart failure NYHA Class 3 or 4)
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
NB32
PBO
Arm Description
Outcomes
Primary Outcome Measures
Percentage of Participants With a Confirmed Occurrence of Major Adverse Cardiovascular Event (MACE)
The primary endpoint is the time from randomization to the first confirmed occurrence of any event within the primary MACE composite (defined as cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke). Due to early termination of the study, pre-planned 50% interim analysis is considered the primary analysis for outcome measures. The pre-planned 50% interim analysis was conducted when 50% of the total planned MACE were observed.
Secondary Outcome Measures
Percentage of Participants With a Confirmed Occurrence of Cardiovascular Death, Nonfatal Myocardial Infarction, Nonfatal Stroke, or Nonfatal Unstable Angina Requiring Hospitalization
Due to early termination of the study, the pre-planned 50% interim analysis is considered the primary analysis for outcome measures.
Percentage of Participants With a Confirmed Occurrence of Cardiovascular Death (Including Fatal Myocardial Infarction, Fatal Stroke)
Due to early termination of the study, the pre-planned 50% interim analysis is considered the primary analysis for outcome measures.
Percentage of Participants With a Confirmed Occurrence of Myocardial Infarction (Nonfatal or Fatal)
Due to early termination of the study, the pre-planned 50% interim analysis is considered the primary analysis for outcome measures.
Percentage of Participants With a Confirmed Occurrence of Stroke (Nonfatal or Fatal)
Due to early termination of the study, the pre-planned 50% interim analysis is considered the primary analysis for outcome measures.
Full Information
NCT ID
NCT01601704
First Posted
May 14, 2012
Last Updated
February 24, 2017
Sponsor
Orexigen Therapeutics, Inc
1. Study Identification
Unique Protocol Identification Number
NCT01601704
Brief Title
Cardiovascular Outcomes Study of Naltrexone SR/Bupropion SR in Overweight and Obese Subjects With Cardiovascular Risk Factors (The Light Study)
Official Title
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Assessing the Occurrence of Major Adverse Cardiovascular Events (MACE) in Overweight and Obese Subjects With Cardiovascular Risk Factors Receiving Naltrexone SR/Bupropion SR
Study Type
Interventional
2. Study Status
Record Verification Date
April 2016
Overall Recruitment Status
Terminated
Study Start Date
June 2012 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
August 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Orexigen Therapeutics, Inc
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine the effects of NB relative to placebo on major adverse cardiovascular events (MACE) such as cardiovascular death, non-fatal myocardial infarction, and non-fatal stroke in overweight and obese subjects who are at a higher risk of having these events because they have diabetes and/or other cardiovascular risk factors.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Overweight
Keywords
Body Weight, Bupropion, Cardiovascular Diseases, Diabetes Mellitus, Diabetes Mellitus, Type 2, Endocrine System Diseases, Glucose Metabolism Disorders, Heart Diseases, Metabolic Diseases, Narcotic Antagonists, Naltrexone, Nutrition Disorders, Obesity, Overnutrition, Overweight
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
8910 (Actual)
8. Arms, Groups, and Interventions
Arm Title
NB32
Arm Type
Experimental
Arm Title
PBO
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
NB32
Other Intervention Name(s)
CONTRAVE
Intervention Description
Naltrexone SR 32 mg/Bupropion SR 360 mg/day. Administered in addition to the weight management program.
Intervention Type
Drug
Intervention Name(s)
PBO
Intervention Description
Placebo. Administered in addition to the weight management program.
Intervention Type
Behavioral
Intervention Name(s)
Weight Management Program
Other Intervention Name(s)
WeightMate (Tm)
Intervention Description
A comprehensive weight management program will be administered in addition to the subject's study medication assignment. The program includes internet counseling by an accredited health and fitness professional and a nutrition and exercise program with goal setting and educational and tracking tools.
Primary Outcome Measure Information:
Title
Percentage of Participants With a Confirmed Occurrence of Major Adverse Cardiovascular Event (MACE)
Description
The primary endpoint is the time from randomization to the first confirmed occurrence of any event within the primary MACE composite (defined as cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke). Due to early termination of the study, pre-planned 50% interim analysis is considered the primary analysis for outcome measures. The pre-planned 50% interim analysis was conducted when 50% of the total planned MACE were observed.
Time Frame
Confirmed occurrence of event between Day 1 (randomization) and up to a maximum of 4 years of follow-up
Secondary Outcome Measure Information:
Title
Percentage of Participants With a Confirmed Occurrence of Cardiovascular Death, Nonfatal Myocardial Infarction, Nonfatal Stroke, or Nonfatal Unstable Angina Requiring Hospitalization
Description
Due to early termination of the study, the pre-planned 50% interim analysis is considered the primary analysis for outcome measures.
Time Frame
Confirmed occurrence of event between Day 1 (randomization) and up to a maximum of 4 years of follow-up
Title
Percentage of Participants With a Confirmed Occurrence of Cardiovascular Death (Including Fatal Myocardial Infarction, Fatal Stroke)
Description
Due to early termination of the study, the pre-planned 50% interim analysis is considered the primary analysis for outcome measures.
Time Frame
Confirmed occurrence of event between Day 1 (randomization) and up to a maximum of 4 years of follow-up
Title
Percentage of Participants With a Confirmed Occurrence of Myocardial Infarction (Nonfatal or Fatal)
Description
Due to early termination of the study, the pre-planned 50% interim analysis is considered the primary analysis for outcome measures.
Time Frame
Confirmed occurrence of event between Day 1 (randomization) and up to a maximum of 4 years of follow-up
Title
Percentage of Participants With a Confirmed Occurrence of Stroke (Nonfatal or Fatal)
Description
Due to early termination of the study, the pre-planned 50% interim analysis is considered the primary analysis for outcome measures.
Time Frame
Confirmed occurrence of event between Day 1 (randomization) and up to a maximum of 4 years of follow-up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
≥50 years of age (women) or ≥45 years of age (men)
Body mass index (BMI) ≥27 kg/m2 and ≤50 kg/m2
Waist circumference ≥88 cm (women) or ≥102 cm (men)
At increased risk of adverse cardiovascular outcomes:
Cardiovascular disease (confirmed diagnosis or at high likelihood of cardiovascular disease) with at least one of the following:
History of documented myocardial infarction >3 months prior to screening
History of coronary revascularization
History of carotid or peripheral revascularization
Angina with ischemic changes (resting ECG), ECG changes on a graded exercise test (GXT), or positive cardiac imaging study
Ankle brachial index <0.9 (by simple palpation) within prior 2 years
≥50% stenosis of a coronary, carotid, or lower extremity artery within prior 2 years
AND/OR
Type 2 diabetes mellitus with at least 2 of the following:
Hypertension (controlled with or without pharmacotherapy at <145/95 mm Hg)
Dyslipidemia requiring pharmacotherapy
Documented low HDL cholesterol (<50 mg/dL in women or <40 mg/dL in men) within prior 12 months
Current tobacco smoker
Exclusion Criteria:
Myocardial infarction within 3 months prior to screening
Angina pectoris Grade III or IV as per the Canadian Cardiovascular Society grading scheme
Clinical history of cerebrovascular disease (stroke)
History of tachyarrhythmia other than sinus tachycardia
Planned bariatric surgery, cardiac surgery, or coronary angioplasty
History of seizures (including febrile seizures), cranial trauma, or other conditions that predispose the subject to seizures
History of mania or current diagnosis of active psychosis, active bulimia or anorexia nervosa (binge eating disorder is not exclusionary)
Any condition with life expectancy anticipated to be less than 4 years (e.g., congestive heart failure NYHA Class 3 or 4)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Medical Director Clinical Science
Organizational Affiliation
Takeda
Official's Role
Study Director
Facility Information:
City
Birmingham
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Alabama
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United States
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Dothan
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Alabama
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United States
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Mobile
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Scottsboro
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Chandler
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Mesa
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Peoria
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Phoenix
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Scottsdale
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Tucson
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Tuscson
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Little Rock
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Anaheim
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Carmichael
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Escondido
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Fresno
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Harbor City
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Huntington Beach
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La Jolla
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Lomita
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Los Angeles
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Paramount
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Pasadena
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Riverside
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Sacramento
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Santa Rosa
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Spring Valley
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Thousand Oaks
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Torrance
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West Hills
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Colorado Springs
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Denver
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Golden
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Wheat Ridge
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Norwalk
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Stamford
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Wilmington
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Delaware
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Washington
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Boynton Beach
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Brooksville
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Clearwater
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Deland
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Delray Beach
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Gainesville
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Jacksonville Beach
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Jacksonville
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Melbourne
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Miami
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New Port Richey
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New Smyrna Beach
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Oakland Park
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Orlando
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Palm Harbor
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Pembroke Pines
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Pensacola
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Pinellas Park
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Saint Petersburg
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Wellington
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Winter Haven
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Atlanta
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Austell
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Columbus
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Lawrenceville
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Riverdale
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Savannah
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Stockbridge
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Chicago
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Gurnee
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Melrose Park
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Bloomington
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Indiana
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Brownsburg
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Indiana
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Elwood
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Evansville
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Hammond
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South Bend
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Valparaiso
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Ames
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Council Bluffs
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Des Moines
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West Des Moines
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Iowa
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Overland Park
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Kansas
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Wichita
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Kansas
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Crestview Hills
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Kentucky
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Louisville
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Mount Sterling
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Kentucky
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Alexandria
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Louisiana
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Baton Rouge
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Louisiana
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Monroe
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Louisiana
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Natchitoches
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Louisiana
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Auburn
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Maine
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Bangor
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Maine
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Baltimore
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Maryland
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Columbia
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Maryland
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Elkridge
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Maryland
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Lutherville
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Salisbury
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Boston
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Brockton
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Massachusetts
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Fall River
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Haverhill
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Massachusetts
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Methuen
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Massachusetts
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Bingham Farms
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Dearbon
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Michigan
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Kalamazoo
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Midland
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Saginaw
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Southfield
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Stevensville
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Edina
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Rochester
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Jackson
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Olive Branch
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Tupelo
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Saint Louis
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Missouri
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Butte
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Montana
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Missoula
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Montana
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Fremont
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Nebraska
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Grand Island
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Nebraska
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United States
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Omaha
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Nebraska
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Henderson
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Nevada
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Las Vegas
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Nevada
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Reno
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Nevada
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United States
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Sparks
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Nevada
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United States
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Belvidere
State/Province
New Jersey
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United States
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Edison
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New Jersey
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United States
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Elizabeth
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New Jersey
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Elmer
State/Province
New Jersey
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Linden
State/Province
New Jersey
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Ridgewood
State/Province
New Jersey
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Albuquerque
State/Province
New Mexico
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United States
City
Bronx
State/Province
New York
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United States
City
Endwell
State/Province
New York
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United States
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New Hyde Park
State/Province
New York
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United States
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New York
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New York
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Staten Island
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New York
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Syracuse
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New York
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Williamsville
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New York
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Cary
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North Carolina
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Charlotte
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Durham
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North Carolina
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Elizabeth City
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North Carolina
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Greensboro
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North Carolina
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Greenville
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North Carolina
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Hickory
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North Carolina
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United States
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Morganton
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North Carolina
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Raleigh
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North Carolina
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Salisbury
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North Carolina
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Wilmington
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North Carolina
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Winston-Salem
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North Carolina
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United States
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Akron
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Ohio
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United States
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Beachwood
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Ohio
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United States
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Cincinnati
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Ohio
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United States
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Cleveland
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Ohio
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United States
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Columbus
State/Province
Ohio
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United States
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Delaware
State/Province
Ohio
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United States
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Kettering
State/Province
Ohio
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United States
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Marion
State/Province
Ohio
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United States
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Mentor
State/Province
Ohio
Country
United States
City
Willoughby Hills
State/Province
Ohio
Country
United States
City
Oklahoma City
State/Province
Oklahoma
Country
United States
City
Medford
State/Province
Oregon
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United States
City
Portland
State/Province
Oregon
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United States
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Altoona
State/Province
Pennsylvania
Country
United States
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Bensalem
State/Province
Pennsylvania
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United States
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Danville
State/Province
Pennsylvania
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United States
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Duncansville
State/Province
Pennsylvania
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United States
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Ephrata
State/Province
Pennsylvania
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United States
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Jersey Shore
State/Province
Pennsylvania
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United States
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Lancaster
State/Province
Pennsylvania
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United States
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Lansdale
State/Province
Pennsylvania
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United States
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Norristown
State/Province
Pennsylvania
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United States
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Scottdale
State/Province
Pennsylvania
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United States
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Sellersville
State/Province
Pennsylvania
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United States
City
State College
State/Province
Pennsylvania
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United States
City
West Reading
State/Province
Pennsylvania
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United States
City
Wilkes-Barre
State/Province
Pennsylvania
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United States
City
Anderson
State/Province
South Carolina
Country
United States
City
Charleston
State/Province
South Carolina
Country
United States
City
Columbia
State/Province
South Carolina
Country
United States
City
Greenville
State/Province
South Carolina
Country
United States
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Greer
State/Province
South Carolina
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United States
City
Hodges
State/Province
South Carolina
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United States
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Laurens
State/Province
South Carolina
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United States
City
Mount Pleasant
State/Province
South Carolina
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United States
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Rapid City
State/Province
South Dakota
Country
United States
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Bristol
State/Province
Tennessee
Country
United States
City
Chattanooga
State/Province
Tennessee
Country
United States
City
Germantown
State/Province
Tennessee
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United States
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Jackson
State/Province
Tennessee
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United States
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Kingsport
State/Province
Tennessee
Country
United States
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Knoxville
State/Province
Tennessee
Country
United States
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Memphis
State/Province
Tennessee
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United States
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Beaumont
State/Province
Texas
Country
United States
City
Corpus Christi
State/Province
Texas
Country
United States
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Dallas
State/Province
Texas
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United States
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Houston
State/Province
Texas
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United States
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Hurst
State/Province
Texas
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United States
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Lake Jackson
State/Province
Texas
Country
United States
City
McKinney
State/Province
Texas
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United States
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San Antonio
State/Province
Texas
Country
United States
City
Schertz
State/Province
Texas
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United States
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Tomball
State/Province
Texas
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United States
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Waco
State/Province
Texas
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United States
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Bountiful
State/Province
Utah
Country
United States
City
Draper
State/Province
Utah
Country
United States
City
Murray
State/Province
Utah
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United States
City
Ogden
State/Province
Utah
Country
United States
City
Orem
State/Province
Utah
Country
United States
City
Salt Lake City
State/Province
Utah
Country
United States
City
West Jordan
State/Province
Utah
Country
United States
City
Alexandria
State/Province
Virginia
Country
United States
City
Norfolk
State/Province
Virginia
Country
United States
City
Richmond
State/Province
Virginia
Country
United States
City
Winchester
State/Province
Virginia
Country
United States
City
Seattle
State/Province
Washington
Country
United States
City
Spokane
State/Province
Washington
Country
United States
City
Tacoma
State/Province
Washington
Country
United States
City
Walla Walla
State/Province
Washington
Country
United States
City
Green Bay
State/Province
Wisconsin
Country
United States
City
Kenosha
State/Province
Wisconsin
Country
United States
City
Madison
State/Province
Wisconsin
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
26954408
Citation
Nissen SE, Wolski KE, Prcela L, Wadden T, Buse JB, Bakris G, Perez A, Smith SR. Effect of Naltrexone-Bupropion on Major Adverse Cardiovascular Events in Overweight and Obese Patients With Cardiovascular Risk Factors: A Randomized Clinical Trial. JAMA. 2016 Mar 8;315(10):990-1004. doi: 10.1001/jama.2016.1558.
Results Reference
derived
Learn more about this trial
Cardiovascular Outcomes Study of Naltrexone SR/Bupropion SR in Overweight and Obese Subjects With Cardiovascular Risk Factors (The Light Study)
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