Phase 2
Completed N=40
Naltrexone and Varenicline: Weight Gain and Tolerability in Cigarette Smokers
Smoking · Nicotine Dependence
Source: ClinicalTrials.gov NCT00502216 ↗
Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Sep 2010
Primary outcomePrimary: Weight Gain in Treatment Completers — 3.35; 4.14 Pounds
Summary
The purpose of this study is to determine whether the combination of naltrexone (Depade) and varenicline (Chantix) minimizes post-smoking cessation weight gain and how well the combination is tolerated.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Weight Gain in Treatment Completers |
3.35; 4.14 | — |
| SECONDARY Weight Gain in Participants Who Are Continuously Abstinent for the Last 4 Weeks of Treatment |
0; 7.67 | — |
| SECONDARY Tolerability of the Combination of 25 mg Naltrexone and 2 mg Varenicline |
10; 4 | — |
Eligibility Criteria
Inclusion Criteria
- Between the ages of 18 and 75
- Smoking 10 or more cigarettes per day
- Fewer than 3 months of smoking abstinence in the past year
- Motivated to stop smoking
Exclusion Criteria
- Current use of opiates, and/or a urine toxicology screen positive for opiates
- Chronic pain conditions necessitating opioid treatment (naltrexone, an opioid antagonist will make these medications ineffective)
- Evidence of significant hepatocellular injury as evidence by AST or ALT >3 x normal or elevated bilirubin
- History of cirrhosis
- Any serious or unstable disease within 6 months
- Seizure risk
- Diabetes mellitus requiring insulin or oral hypoglycemic medications
- Hepatic or renal impairment
- Use of a monoamine oxidase inhibitor in the prior 14 days
- Clinically significant cardiovascular disease within 6 months
- Uncontrolled hypertension
- Baseline systolic blood pressure higher than 150 mm Hg or diastolic blood pressure higher than 95 mm Hg
- Severe chronic obstructive pulmonary disease
- History of cancer (except treated basal cell or squamous cell carcinoma of the skin)
- History of clinically significant allergic reactions
- Major depressive disorder within the past year requiring treatment
- History of or current panic disorder, psychosis, bipolar disorder, or eating disorders
- Alcohol or drug abuse/dependency within the past year
- Use of another investigational drug within 30 days
- Intention to donate blood or blood products during the treatment phase of the study
- Use of tobacco products other than cigarettes or use of marijuana
- Use of nicotine replacement therapy, clonidine, varenicline, bupropion, or nortriptyline within the month prior to enrollment or intention to use medication that might interfere with study medication
- Body Mass Index (calculated as weight in kilograms divided by the square of height in meters) less than 15 or greater than 38 or weight less than 45 kg.
- Females of childbearing potential who are pregnant, nursing, or not practicing effective contraception (oral injectable, or implantable contraceptives, intrauterine device, or barrier method with spermacide)
Data sourced from ClinicalTrials.gov (NCT00502216). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.