Status:
COMPLETED
A Study to Assess the Nicotine Pharmacokinetics, Tolerability and Safety With a New Oral Nicotine Replacement Product in Healthy Japanese Smokers
Lead Sponsor:
Janssen Pharmaceutical K.K.
Conditions:
Healthy
Eligibility:
All Genders
20-50 years
Phase:
PHASE1
Brief Summary
In Part 1, the purpose of this study is to elucidate the single-dose pharmacokinetic profiles of 1 spray and 2 consecutive sprays of oromucosal nicotine spray (ONS) in comparison with those of nicotin...
Eligibility Criteria
Inclusion
- Healthy male or female Japanese participants between the ages of 20 and 50 years, inclusive. Health is defined as the absence of clinically relevant abnormalities identified by a detailed medical history, blood pressure, pulse rate measurements, 12-lead electrocardiogram (ECG) as well as clinical laboratory tests, as judged by the principal investigator or sub investigator.
- Smoking of at least 15 cigarettes daily during at least one year preceding inclusion
- Body Mass Index between 17.5 and 30.0 kilogram per square meter (kg/m\^2) and a total body weight greater than or equal to (\>=) 50.0 kg
- Evidence of a personally signed and dated informed consent document indicating that the participant has been informed of all pertinent aspects of the study
- All women of childbearing potential, except for postmenopausal females, must have a negative urine beta-human chorionic gonadotropin (beta-hCG) at screening of Part 1 and all planned visits of Part 1 and Part 2
Exclusion
- Evidence or history of an acute or chronic medical or psychiatric condition or allergy or laboratory abnormality, or of use of drugs that, in the judgment of the principal investigator or sub investigator, increase the risk associated with study participation or interfere with the interpretability of study results
- Females: Pregnancy, breast-feeding, premenopausal, or perimenopausal state with insufficient contraception
- Treatment with an investigational drug within 3 months preceding the first dose of study product
- Participant has donated blood or blood product or had substantial loss of blood more than 200 milliliter (mL) within 1 month before study products administration, or greater than or equal to (\>=) 400 mL within 3 months for males and 4 months for females before study products administration, or participant has donated a total volume of blood in the past one year exceeding 1,200 mL for males and 800 mL for females, or participant has an intention to donate blood or blood products during the study and for at least 3 months for males and 4 months for females for blood, or at least 2 months for both genders for blood products after completion of the study
- Exclusion Criterion for Only Part 2: participants who is analyzed as cytochrome (CYP)2A6 \*4/\*4 by CYP2A6 genetic polymorphism test at Visit 1 of Part 1
Key Trial Info
Start Date :
December 22 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 16 2018
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT03398876
Start Date
December 22 2017
End Date
April 16 2018
Last Update
February 3 2025
Active Locations (1)
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1
Souseikai Hakata Clinic
Fukuoka, Japan, 8120025