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A Phase 2, Seven Week, Double-Blind, Placebo Controlled, Randomized, Parallel Group Study To Evaluate The Safety And Efficacy Of Three Doses Of A Controlled Release Formulation Of Varenicline For Smoking Cessation
The purpose of this study is to evaluate the safety, efficacy, and tolerability of twice daily (BID) administration of three dose strengths (1.2 mg, 1.8 mg, and 2.4 mg) of varenicline controlled release (CR) tablets in adult smokers.
Details
| Lead sponsor | Pfizer |
|---|---|
| Phase | Phase 2 |
| Status | WITHDRAWN |
| Start date | 2010-08 |
| Completion | 2011-08 |
Conditions
- Smoking Cessation
Interventions
- Varenicline Controlled Release 1.2 mg
- Varenicline Controlled Release 1.8 mg
- Varenicline Controlled Release 2.4 mg
- Varenicline Immediate Release 1 mg
- Placebo
Primary outcomes
- Continuous abstinence from smoking for weeks 4-7, carbon monoxide confirmed — 7 weeks