Status:
COMPLETED
A Safety and Efficacy Study of Naltrexone SR/Bupropion SR and Placebo in Overweight and Obese Subjects Participating in an Intensive Behavior Modification Program
Lead Sponsor:
Orexigen Therapeutics, Inc
Conditions:
Obesity
Overweight
Eligibility:
All Genders
18-65 years
Phase:
PHASE3
Brief Summary
The purpose of this study is to determine whether a combination of naltrexone SR and bupropion SR is safe and effective in treating obesity and leads to greater weight loss when given with a group lif...
Detailed Description
The combination of group lifestyle modification counseling and pharmacotherapy has recently been shown to result in nearly twice the average weight loss at one year (12.1 kg) as pharmacotherapy alone ...
Eligibility Criteria
Inclusion
- Female or male subjects aged 18 to 65 years (inclusive)
- Body mass index (weight \[kg\]/height \[m²\]) ≥30 and ≤45 kg/m² for subjects with uncomplicated obesity, and BMI of ≥27 and ≤45 kg/m² for subjects with controlled hypertension and/or dyslipidemia
- Non-smoker and had not used tobacco or nicotine products for at least 6 months before screening
- Normotensive (systolic ≤140 mm Hg and diastolic ≤90 mm Hg). Anti-hypertensive medications were allowed with the exception of alpha-adrenergic blockers, beta-blockers, and clonidine. Medical regimen was to be stable for at least 8 weeks.
- Low-density lipoprotein level \<190 mg/dL and triglycerides level \<400 mg/dL. Medications for the treatment of dyslipidemia were allowed as long as the medical regimen had been stable for at least 8 weeks.
- No clinically significant abnormality of serum albumin, blood urea nitrogen (BUN), creatinine, bilirubin, calcium and phosphorus
- Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) within 2.5 times upper limit of normal (ULN)
- No clinically significant abnormality of hematocrit, white blood cell (WBC) count, WBC differential, or platelets
- Fasting glucose ≤126 mg/dL and not receiving hypoglycemic agents
- No clinically significant abnormality on urinalysis
- Thyroid stimulating hormone (TSH) within 1.5 times ULN or normal triiodothyronine (T3), if TSH was below normal limits
- Female subjects of childbearing potential had a negative serum pregnancy test
- An IDS-SR score \<2 on individual items: 5 (sadness), 6 (irritability), 7 (anxiety/tension), and 18 (suicidality) and an IDS-SR total score \<30
- Female subjects of childbearing potential were non-lactating and agreed to continue to use effective contraception throughout the study and 30 days after discontinuation of study drug
- Completed a food diary for 6 of 7 consecutive days during screening
- Able to comply with all required study procedures and schedule
- Able to speak and read English
- Provided written informed consent
Exclusion
- Obesity of known endocrine origin (e.g., untreated hypothyroidism, Cushing's syndrome, established polycystic ovary syndrome)
- Serious medical condition (including but not limited to renal or hepatic insufficiency; congestive heart failure, angina pectoris, myocardial infarction, stroke, claudication, or acute limb ischemia; history of malignancy with exception of non-melanoma skin cancer or surgically cured cervical cancer)
- Serious psychiatric illness (e.g., lifetime history of bipolar disorder, schizophrenia or other psychosis, bulimia, and anorexia nervosa; current serious personality disorder, e.g., borderline; severe major depressive disorder, recent \[previous 6 months\] suicide attempt or current active suicidal ideation, recent hospitalization due to psychiatric illness)
- Response to the bipolar disorder questions that indicated the presence of bipolar disorder.
- Required medications for the treatment of a psychiatric disorder (with the exception of short-term insomnia) within the previous 6 months
- History of drug or alcohol abuse or dependence within 1 year
- Type I or Type II diabetes mellitus
- Baseline ECG with a corrected QT (QTc) interval (using Bazett's formula \>450 millisecond (msec) \[males\] and \>470 msec \[females\]) or the presence of any clinically significant cardiac abnormalities, including but not limited to patterns consistent with myocardial ischemia, electrolyte abnormalities, or atrial or ventricular dysrhythmia or significant conduction abnormalities
- Received excluded concomitant medications: any psychotropic agents (including antipsychotic, antidepressant, anxiolytic, mood stabilizer or anticonvulsant agents) with the exception of low-dose benzodiazepine or hypnotic agents for the treatment of insomnia; any anorectic or weight loss agents; any over-the-counter dietary supplements with psychoactive, appetite or weight effects; alpha-adrenergic blockers; beta-blockers; clonidine; coumadin; theophylline; cimetidine; oral corticosteroids; topiramate, Depo-Provera®; smoking cessation agents; regular use of opioid or opioid-like analgesics
- History of surgical or device (e.g., lap band) intervention for obesity
- History of seizures of any etiology, or of predisposition to seizures (e.g., history of cerebrovascular accident, head trauma with \>5 minutes loss of consciousness, concussion symptoms lasting \>15 minutes, brain surgery, skull fracture, subdural hematoma, or febrile seizures)
- History of treatment with bupropion or naltrexone within the preceding 12 months
- History of hypersensitivity or intolerance to bupropion or naltrexone
- Used drugs, herbs, or dietary supplements believed to significantly affect body weight or participated in a weight loss management program within one month prior to baseline
- Loss or gained \>4.0 kilograms within the previous 3 months
- Females who were pregnant or breast-feeding or planning to become pregnant during the study period or within 30 days of discontinuing study drug
- Planned surgical procedure that could impact the conduct of the study
- Received any investigational drug or used an experimental device or procedure within the previous 30 days
- Participated in any previous clinical trial conducted by Orexigen
- Had any condition that in the opinion of the investigator made the subject unsuitable for inclusion into the study
Key Trial Info
Start Date :
March 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2008
Estimated Enrollment :
793 Patients enrolled
Trial Details
Trial ID
NCT00456521
Start Date
March 1 2007
End Date
December 1 2008
Last Update
December 17 2014
Active Locations (9)
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1
University of California, San Diego: Dept of Family & Preventive Medicine
La Jolla, California, United States, 92093
2
Center for Human Nutrition, University of Colorado Health Services Center
Denver, Colorado, United States, 80220
3
Univ. of Florida, College of Public Health, and Health Professions
Gainesville, Florida, United States, 32611
4
Washington Univ. Center for Human Nutrition
St Louis, Missouri, United States, 63110