drugset / Trial / NCT00141167

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

NCT00141167 ↗

Phase 3 Completed 250 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 for smoking cessation.

Timeline

Start
2005-02
Primary completion
—
Completion
2006-01

Outcome

Met primary endpoint

paper Smoking-cessation rates at the end of treatment were 59.5% with varenicline versus 32.3% with placebo (P < 0.001). PMID 17692719 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Varenicline Small molecule 1 mg —

Indications

No indication recorded.