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Bioequivalence Between an Oral Nicotine Replacement Product and Nicorette® Gum

NCT01152749 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2012-07-10

No results posted yet for this study

Summary

This study examines the bioequivalence between an oral nicotine replacement product and Nicorette® gum.

Conditions

  • Tobacco Dependence

Interventions

DRUG

Nicotine

Single-dose of new NRT product

DRUG

Nicotine Gum

Single-dose of marketed nicotine gum

Sponsors & Collaborators

  • McNeil AB

    lead INDUSTRY

Principal Investigators

  • Elisabeth Kruse, PhD · McNeil AB

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
CROSSOVER

Eligibility

Min Age
19 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-12-31
Primary Completion
2010-03-31
Completion
2010-05-31

Countries

  • Sweden

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01152749 on ClinicalTrials.gov