An Investigation Of The Effects Of Food On The Absorption Of A Varenicline Controlled Release Formulation

Completed · Phase 1

Conditions studied: Pharmacokinetics, Bioavailability, Smoking Cessation

In brief

1. To estimate the absorption of a single oral dose of a controlled release varenicline tablet under fed and fasted conditions. 2. To evaluate the pharmacokinetics, safety, and tolerability of a single dose of a varenicline controlled release tablet under fed and fasted conditions.

Key facts

Study ID

NCT00731562

Run by

Pfizer

People needed

24

Starts

2008-07-01

Expected to finish

2008-09-01

Last updated by the study team

2010-01-11

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy male or female adult smokers
• 18 to 55 years of age

You may not qualify if…

• Sensitivity to varenicline
• Illegal drug use
• Pregnant or nursing females

Where it is running

• Pfizer Investigational Site — East Grand Forks, Minnesota, United States
• Pfizer Investigational Site — Fargo, North Dakota, United States

Full record on ClinicalTrials.gov

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