Elsevier

Clinical Therapeutics

Volume 29, Issue 6, June 2007, Pages 1040-1056
Clinical Therapeutics

Efficacy and tolerability of varenicline, an α4β2 nicotinic acetylcholine receptor partial agonist, in a 12-week, randomized, placebo-controlled, dose-response study with 40-week follow-up for smoking cessation in Japanese smokers*

https://doi.org/10.1016/j.clinthera.2007.06.012Get rights and content

Abstract

Background:

Varenicline, a selective α4β2 nicotinic acetylcholine receptor partial agonist, has been developed specifically for smoking cessation. In Japan, 39.3% of men smoke and this is a major public health concern.

Objective:

The primary objective of this study was to evaluate the efficacy and dose-response relationship of varenicline in Japanese smokers.

Methods:

In this double-blind, placebo-controlled, randomized, parallel-group study, subjects were randomized to receive varenicline at 0.25 mg BID, 0.5 mg BID, 1 mg BID, or placebo for 12 weeks followed by a 40-week, nontreatment follow-up phase. The primary efficacy variable was the continuous abstinence rate (CAR), defined as no reported smoking (not even a puff) or other nicotine use and confirmed by end-expiratory carbon monoxide level ≤10 ppm, during the last 4 weeks of treatment (weeks 9–12). Secondary end points included CARs for weeks 9–24 and 9–52. Craving, withdrawal, and smoking satisfaction were determined by the Minnesota Nicotine Withdrawal Scale, the Brief Questionnaire on Smoking Urges, and the modified Cigarette Evaluation Questionnaire. The tolerability of varenicline was also evaluated.

Results:

Of 618 subjects who received treatment, 515 (83.3%) were classified as nicotine dependent (scoring ≥5 on the Tobacco Dependence Screener), and constituted the primary analysis group. Of these, 385 (74.8%) subjects were male, and the mean age was within the range of 39.0 to 40.2 years. Across treatment groups, subjects claimed to have smoked a mean of 23.1 to 24.9 cigarettes per day in the preceding 30 days, and the mean score on the Fagerström Test for Nicotine Dependence was within the range from 5.4 to 5.7. The CAR for weeks 9–12 was significantly higher for all doses of varenicline compared with placebo (39.5% [51/129]). The highest CAR of 65.4% (85/130) was achieved with varenicline 1 mg BID (odds ratio [OR] [95% CI] = 2.98 [1.78–4.99]; P < 0.001). The CAR for weeks 9–52 was significantly greater for varenicline 1 mg BID than placebo (34.6% [45/130] vs 23.3% [30/129]; OR [95% CI] = 1.81 [1.04–3.17]; P = 0.036). The CARs for weeks 9–24 at 0.25, 0.5, and 1 mg BID were 33.6% (43/128), 35.2% (45/128), 37.7% (49/130), and for weeks 9–52 at 0.25 and 0.5 mg BID were 27.3% (35/128) and 28.9% (37/128) but failed to reach significance versus the placebo (29.5% [38/129] for weeks 9–24 and 23.3% [30/129] for weeks 9–52). Treatment-emergent adverse events (AEs) were more prevalent among varenicline-treated subjects (79.1% [121/153] at 0.25 mg BID, 80.6% [125/155] at 0.5 mg BID, and 80.1% [125/156] at 1 mg BID) than placebo subjects (71.4% [110/154]). The 3 most prevalent AEs at varenicline 1 mg BID were nasopharyngitis (35.9% [56/156]), nausea (24.4% [38/156]), and headache (10.3% [16/156]), all of which were of mild or moderate intensity. Nausea was the only AE that appeared dose related (7.2% [11/153] at 0.25 mg BID, 9.7% [15/155] at 0.5 mg BID, and 24.4% [38/156] at 1 mg BID) versus placebo (7.8% [12/154]).

Conclusions:

Varenicline was associated with dose-dependent improvement in smoking abstinence rates during the last 4 weeks of treatment and in the longer term over 40 weeks of nontreatment follow-up. The dose associated with the highest efficacy was varenicline 1 mg BID.

References (36)

  • SilagyC et al.

    Nicotine replacement therapy for smoking cessation

    Cochrane Database Syst Rev

    (2004)
  • HughesJR et al.

    Antidepressants for smoking cessation

    Cochrane Database Syst Rev

    (2007)
  • US Dept of Health and Human Services

    The health consequences of smoking: Nicotine addiction: A report of the Surgeon General

    (1988)
  • HenningfieldJ et al.

    Pathophysiology of tobacco dependence

  • MaskosU et al.

    Nicotine reinforcement and cognition restored by targeted expression of nicotinic receptors

    Nature

    (2005)
  • CoeJW et al.

    Varenicline: An alpha4beta2 nicotinic receptor partial agonist for smoking cessation

    J Med Chem

    (2005)
  • JorenbyDE et al.

    Efficacy of varenicline, an alpha4beta2 nicotinic acetylcholine receptor partial agonist, vs placebo or sustained-release bupropion for smoking cessation: A randomized controlled trial [published correction appears in JAMA. 2006;296:1355]

    JAMA

    (2006)
  • GonzalesD et al.

    Varenicline, an alpha4beta2 nicotinic acetylcholine receptor partial agonist, vs sustained-release bupropion and placebo for smoking cessation: A randomized controlled trial

    JAMA

    (2006)
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    *

    The data in this manuscript were presented in part at the 2006 Scientific Sessions of the American Heart Association, November 12–15, 2006, Chicago, Illinois.

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