drugset / Trial / NCT00141206

A Twelve-Week Study of Varenicline for Safety and Efficacy in Comparison With Placebo and Zyban for Smoking Cessation

NCT00141206 ↗

Phase 3 Completed 1005 enrolled Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of this study is to evaluate the safety and efficacy of varenicline given for a twelve week treatment period in comparison with placebo and Zyban for smoking cessation.

Timeline

Start
2003-05
Primary completion
—
Completion
2005-04

Outcome

Met primary endpoint

paper For weeks 9 through 12, the 4-week continuous abstinence rates were 44.0% for varenicline vs 17.7% for placebo PMID 16820546 ↗

paper Varenicline was significantly more efficacious than placebo for smoking cessation at all time points PMID 16820546 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Varenicline Small molecule 1 mg Oral

Indications

No indication recorded.