Pfizer Investigational Site
New Haven, Connecticut, 06511, United States
NCT Number: NCT00774605
To evaluate the absorption, safety, and tolerability of a varenicline solution and a varenicline patch applied to the skin.
Looking for future studies?
Notify Me18 year–55 year
Male
Interventional
Phase 1
New Haven, Connecticut, 06511, United States
Additional Study Purpose Details: Evaluation of the pharmacokinetic profile of a varenicline solution and a varenicline patch applied to the skin
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A single application of a 4.8 mg varenicline solution will be applied to the upper back over a 24 hour period
A single application of a nominal 1.2 mg dose of a varenicline transdermal delivery system (5 cm2 patch, 4.8 mg drug payload) will be applied to the upper back over a 24 hour period
Time frame: 8 days
Time frame: 8 days
Looking for future studies?
Notify MePfizer
Industry
A Phase 1, Open-Label, Nonrandomized, Single Dose Study To Characterize The Pharmacokinetics Of A Varenicline (CP-526,555) Transdermal Solution And A Varenicline Transdermal Delivery System Applied To The Skin Of Adult Smokers
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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