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Oral Mucosal Effects In Adult Smokers Associated With Two Nicotine Lozenge Formulations

Safety Issues Clinical Trial

Official title:
Randomized, Parallel-Group, Assessor Blind Study To Evaluate Oral Mucosal Effects In Healthy Adult Smokers Associated With 3 Week Use Of Nicotine Bi-tartrate 4mg Mint Lozenges Relative To The Use Of Nicotine Polacrilex 4mg Mint Lozenges

Clinical Trial Summary

To study the oral mucosal effects in adult smokers associated with the use of two Nicotine Lozenge formulations.

Clinical Trial Description

To assess the oral mucosal health associated with 3 weeks of use of test product, Nicotine Bitartrate 4 mg mint lozenge, relative to a reference product, Nicorette® [Nicotine Polacrilex] 4 mg mint lozenge, in healthy adult smokers motivated to quit smoking. To evaluate the safety and tolerability of Nicotine Bitartrate 4 mg mint lozenge and Nicorette® [Nicotine Polacrilex] 4 mg mint lozenge in this subject population. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03087786
Study type Interventional
Source Niconovum USA
Contact
Status Completed
Phase Phase 1
Start date March 21, 2017
Completion date August 13, 2017
View Details
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