This study will consist of 2 phases. Phase 1 will be a one day crossover study to see the effects of study product on a smoker's desire to smoke, measured by changes in scores on questionnaires given over time. Phase 2 will be a two-week extension, in which subjects will self-administer the study product and visit the study site for assessment of desire to smoke and collection of samples for the evaluation of smoking-related biomarkers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
SINGLE
Enrollment
109
one dissolvable bit, one time, after a period of abstinence from smoking
one dissolvable bit, one time, after a period of abstinence from smoking
Comfort Inn
Martinsburg, West Virginia, United States
effect on subject's craving to smoke
craving is assessed by changes in questionnaire answers over time
Time frame: 5 hours
adverse events related to study product
collection of information on adverse events related to study product
Time frame: 5 hours
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