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Phase 2 Completed N=40 Randomized Triple-blind Treatment

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

OutcomeResultp-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)
View full record on ClinicalTrials.gov →

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.

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