@article {Williams:April 2007:0300-7995:793,
author = "Williams, Kathryn E.",
author = "Reeves, Karen R.",
author = "Billing, Clare B.",
author = "Pennington, Ann M.",
author = "Gong, Jason",
title = "A double-blind study evaluating the long-term safety of varenicline for smoking cessation",
journal = "Current Medical Research and Opinion",
volume = "23",
year = "April 2007",
abstract = "Objective: We assessed the safety of long-term varenicline administration for smoking cessation.Methods: In this randomized, double-blind, multicenter trial, eligible adult smokers (18-75 years) who smoked an average of ≥10 cigarettes/day were randomized to either varenicline 1 mg twice daily (BID) or placebo for 52 weeks. Subjects made weekly clinic visits until week 8, and then every 4 weeks until week 52, with a follow-up visit at week 53. The target quit date was the morning of the week 1 clinic visit. Brief counseling was provided at each visit, and vital signs, adverse events (AEs), and smoking status were documented. Other laboratory measures were collected at specified visits.Results: A total of 251 subjects were randomized to varenicline and 126 to placebo. Approximately half of the subjects in each arm completed the study (53.8% varenicline; 46.8% placebo). Treatment-emergent AEs were observed in 96.4% of varenicline- and 82.5% of placebo-treated subjects during the study. Common varenicline-associated AEs were nausea (40.2%), abnormal dreams (22.7%), and insomnia (19.1%). Most AEs were considered mild or moderate in intensity. AEs leading to discontinuation of varenicline treatment included nausea (7.6%), insomnia (3.2%), and abnormal dreams (2.4%). A single varenicline-related serious AE, bilateral subcapsular cataracts, was observed. At week 52, 7-day point prevalence abstinence rates were 36.7% (varenicline) and 7.9% (placebo).Conclusions: Varenicline 1 mg BID can be safely administered for up to 1 year. Varenicline was also a more effective smoking cessation aid than placebo throughout the study, supporting both its short- (12-week) and long-term (52-week) efficacy.",
pages = "793-801(9)",
url = "http://www.ingentaconnect.com/content/apl/cmro/2007/00000023/00000004/art00014"
doi = "doi:10.1185/030079907X182185"
}