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Completed

NCT Number: NCT02688374

A Bioequivalence Study of Three, 2 mg Nicotine Chewing Gums (Two Tests and One Reference) in Healthy Adult Smokers

This is a randomized, open-label, single-dose, three-period, crossover, single-center comparative bioavailability (BA) study under fasting condition in Chinese healthy male adult participants with a history of cigarette smoking. The participants will be admitted to the investigational clinic at least 38 hours before dosing and will remain domiciled until the completion of all study procedures at approximately 24 hours after dosing. Three toothpastes (one is commercial non-medicated non-nicotine containing chewing gum and other two are nicotine containing gums) will be provided across the 3 treatment periods. During each of the 3 treatment periods, participants will be under supervision in a non-smoking area and will abstain from smoking.There will be a total of at least 7 days and not more than 10 days (clinical furlough period) between treatment periods. Twenty (20) blood samples will be collected for pharmacokinetic (PK) analysis at baseline and multiple time points following study drug administration. The trial duration will be approximately 49 days and up to 55 days from screening to study end including the screening period.

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Key information

Conditions

Tobacco Use Disorder Chemically-Induced Disorders Mental Disorders Substance-Related Disorders

Age range

18 year–45 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

GSK Investigational Site

Beijing, 100032, China

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants must understand and provide written informed consent before any assessment is performed, understand the study procedures, and be willing to complete the required assessments and the study.
  • Chinese male participants between 18 and 45 years of age (inclusive) in general good physical health as judged by the Investigator.
  • Normal vital signs as follows:
  • Oral body temperature between 35.0 and 37.5 ºC (95 and 99.5 F) inclusive
  • Supine systolic blood pressure between 90 and 140 mmHg inclusive
  • Supine diastolic blood pressure between 55 and 90 mmHg inclusive
  • Pulse rate between 50 and 100 beats per minute (bpm) inclusive
  • History of cigarette smoking of at least 10 cigarettes per day continuously for the past 3 months prior to screening.
  • Body weight ≥ 50 kg, Body Mass Index (BMI) between 19 and 28 at screening.
  • Ability to communicate and comply with all study requirements including the study specific chewing and swallowing procedures.

Exclusion criteria

-

  • Use of other investigational drugs within 30 days or 10 half-lives of enrollment, whichever is longer.
  • History of or known hypersensitivity to the study drug or excipients.
  • Diagnosis of long QT syndrome or QTc > 450 msec for males at screening.
  • Any surgical or medical condition which may significantly alter the absorption, distribution, metabolism or excretion of any drug substance.
  • History of malignancy or neoplastic disease of any organ system treated or untreated, orthostatic hypotension, cardiovascular disease, stroke, TIA, fainting or blackouts, clinically significant metabolic, pulmonary, neurological, hematological, autoimmune, psychiatric or endocrine disorders.. within the past 5 years prior to screening.
  • Any evidence of cardiovascular, pulmonary, renal, hepatic, gastrointestinal, hematological, endocrinological, metabolic, autoimmune, neurological, psychiatric, other diseases or other clinically significant laboratory findings at screening.
  • Participant has used any medication within two weeks before first scheduled study drug administration or within less than 10 times the elimination half-life of the respective drug.
  • Unable to comply with the chewing and/or swallowing rhythm requirements (> 5% deviation of the total counts over 30 minutes) after trying either one of the two training sessions for 3 times.
  • CO > 12 ppm after at least 38 hours confinement period in clinics prior to first dosing.
  • Participants reports consumption of any drug metabolizing enzyme inducing or inhibiting aliments, evidence of current alcohol abuse or reports consumption exceeding 35 g of pure alcohol per day.
  • Any history of drug hypersensitivity, asthma, urticaria, or other significant allergic diathesis, positive results in any of the virology tests for Human immunodeficiency virus (HIV)-Ab, Hepatitis C virus (HCV)-Ab, Surface antigen of the hepatitis B virus (HBs-Ag), and Tp-Ab.
  • Participation in a previous clinical study with or without another investigational product and with ~470 ml blood drawn, or blood donation within the last 3 months prior to screening or previous enrollment into the current study.
  • Vulnerable individual
  • Inability to be venipuncture and/or tolerate venous access, unwilling to accept slight irritation of the throat and increased salivation due to nicotine gum administration.
  • Unable or unwilling to discontinue the use or consumption of cigarette smoking, any nicotine containing products, Oral, local or topical pharmaceutical agents, consumption of caffeine/theophylline - containing products, grapefruit, Seville orange, orange, lemon, lime, apple, and pineapple, performance of unaccustomed strenuous physical exercise.

Treatment and study plan

Treatment A: Nicorette 2 mg coated mint gum

Other

Participants will be administered with 2 mg coated mint gum of Nicorette

Treatment B: Nicotinell 2 mg coated mint gum

Other

Participants will be administered with 2 mg coated mint gum of Nicotinell

Treatment C: Nicotinell 2 mg coated fruit flavor gum

Other

Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell

Primary outcomes

  1. Area under the curve from time zero to last sampling time [AUC(0-t)]

    Time frame: 2 days

    AUC(0-t) will be calculated using the trapezoidal rule. Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.

  2. Area under the curve from time zero extrapolated to infinity [AUC(0-inf)]

    Time frame: 2 days

    The area under the plasma concentration versus time curve will be calculated from time 0 to infinity where AUC = AUClast + Clast/λz Clast is the concentration at the last measurable sampling time point and λz is the terminal elimination rate constant. Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.

  3. Maximum plasma concentration (Cmax)

    Time frame: 2 days

    Cmax will be obtained graphically from the plasma concentration over time profile. Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.

  4. Time to reach maximum plasma concentration (Tmax)

    Time frame: 2 days

    Tmax will be obtained graphically from the plasma concentration over time profile. Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.

  5. Termination rate constant (Lambda_z)

    Time frame: 2 days

    Lambda_z will be computed as the slope of the regression line of ln (C(t)) on time. Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.

  6. Elimination half life (t1/2)

    Time frame: 2 days

    T1/2 will be computed as T1/2 = 0.693/ λz. Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.

  7. Systemic clearance (CL/F)

    Time frame: 2 days

    CL/F will be calculated as the Dose/AUCinf, where Dose is the actual nicotine dose released. Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.

  8. Apparent volume of distribution (Vd/F)

    Time frame: 2 days

    Vd/F will be determined by the following equation: Vz/F = Dose/(lambda_z · AUCinf), where Dose is the actual nicotine dose released. Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.

Sponsors and collaborators

Lead sponsor

GlaxoSmithKline

Industry

Registry information

Official study title

A Single-Dose, Open-Label, Three-way Crossover Bioequivalence Study of Three, 2 mg Nicotine Chewing Gums (Two Tests and One Reference) in Chinese Male Healthy Adult Smokers

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Feb 23, 2016
Registry last updated
Dec 19, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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