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Clin Pharmacol Drug Dev ; 7(5): 498-505, 2018 06.
Article in English | MEDLINE | ID: mdl-29193747

ABSTRACT

Diverse nicotine replacement therapy options may improve consumer usage. This study was conducted to establish the bioequivalence of a new cherry-flavored mini lozenge with that of a currently marketed mint-flavored mini lozenge. The rate (Cmax ) and extent (AUC0-t ) of plasma nicotine absorption were compared after administration of 2- and 4-mg doses of each lozenge in healthy adult smokers (n = 43). The bioequivalence of each respective dose was established based on the 90% confidence interval for the ratio of geometric means for both Cmax and AUC0-t lying within the range of 0.80 to 1.25. Adverse-event profiles were similar between formulations.


Subject(s)
Flavoring Agents/chemistry , Smoking Cessation Agents/administration & dosage , Smoking Cessation Agents/pharmacokinetics , Adult , Area Under Curve , Cross-Over Studies , Dose-Response Relationship, Drug , Drug Compounding , Female , Healthy Volunteers , Humans , Male , Middle Aged , Smoking Cessation Agents/chemistry , Therapeutic Equivalency , Tobacco Use Cessation Devices/adverse effects , Young Adult
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