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Clinical Trial Summary

The purpose of this study is to evaluate the bioequivalence of a new transdermal nicotine patch to that of a reference formulation following repeated applications


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Crossover Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT02089308
Study type Interventional
Source Pierre Fabre Medicament
Contact
Status Completed
Phase Phase 1
Start date March 2014
Completion date May 2014

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