Nicotine Lozenge Bioequivalence Study
Completed · Phase 1
Conditions studied: Smoking Cessation
In brief
To compare the bio equivalence of new nicotine lozenge formulation with the reference nicotine lozenge so as to deliver the same nicotine blood profile.
Key facts
- Study ID
- NCT01536704
- Run by
- GlaxoSmithKline
- People needed
- 50
- Starts
- 2011-07-01
- Expected to finish
- 2011-08-01
- Last updated by the study team
- 2013-04-26
Who can join
Age: 19 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Participants must be healthy smokers who usually smoked their first cigarette within 30 minutes of waking.
- Body Mass Index within the range 19-27 kilograms/meters\^2
You may not qualify if…
- Participants who used chewing tobacco or tobacco products other than cigarettes within 21 days of screening visit
Where it is running
- Celerion NEBRASKA — Lincoln, Nebraska, United States
Full record on ClinicalTrials.gov
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