Last updated: 11/09/2021 06:30:09

A Bioequivalence Study of 21 milligram (mg) Nicotine Transdermal Patches (NicoDerm CQ, GlaxoSmithKline [GSK] Dungarvan) Compared to the Current Marketed 21 mg Nicotine Transdermal Patches (NicoDerm CQ, Alza) in Healthy Adult Smokers

GSK study ID
217756
Clinicaltrials.gov ID
NCT05024747
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Completed
Completed
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: A Randomized, Open Label, Single Center, Single Dose, two Period, two Sequence Crossover Bioequivalence Study of 21 mg Nicotine Transdermal Patches (NicoDerm CQ, GSK Dungarvan) Compared to the Current Marketed 21 mg Nicotine Transdermal Patches (NicoDerm CQ, Alza) in Healthy Adult Smokers
Trial description: The purpose of this study is to assess the bioequivalence of the 21mg nicotine transdermal patch from GSK Dungarvan (Test) compared to the 21mg nicotine transdermal patch currently manufactured by Alza (Reference).
Primary purpose:
Other
Trial design:
Crossover Assignment
Masking:
None (Open Label)
Allocation:
Randomized
Primary outcomes:

Assessment of Bioequivalence of NicoDerm CQ, GSK Dungarvan with NicoDerm CQ, Alza by Measuring Maximum Observed Plasma Nicotine Concentration (Cmax)

Timeframe: Predose (within 1 hour before dosing), 0.5, 1, 2, 3, 4,5, 6, 8, 10, 12, 14, 16, 18, 20, 24, 25, 26, 27, 28, 30, 32, and 36 hours postdose in each treatment period

Assessment of Bioequivalence of NicoDerm CQ (GSK Dungarvan) with NicoDerm CQ (Alza) by Measuring Area Under the Plasma Concentration Versus Time Curve From Time Zero to Time t (AUC [0-t])

Timeframe: Predose (within 1 hour before dosing), 0.5, 1, 2, 3, 4,5, 6, 8, 10, 12, 14, 16, 18, 20, 24, 25, 26, 27, 28, 30, 32, and 36 hours postdose in each treatment period

Assessment of Bioequivalence of NicoDerm CQ (GSK Dungarvan) with NicoDerm CQ (Alza) by Measuring Area Under the Plasma Concentration Versus Time Curve Calculated from Time Zero to Infinity (AUC [(0-inf])

Timeframe: Predose (within 1 hour before dosing), 0.5, 1, 2, 3, 4,5, 6, 8, 10, 12, 14, 16, 18, 20, 24, 25, 26, 27, 28, 30, 32, and 36 hours postdose in each treatment period

Secondary outcomes:

Assessment of Pharmacokinetic Profile of the Patches by Measuring Lambda z (λz)

Timeframe: Predose (within 1 hour before dosing), 0.5, 1, 2, 3, 4,5, 6, 8, 10, 12, 14, 16, 18, 20, 24, 25, 26, 27, 28, 30, 32, and 36 hours postdose in each treatment period

Assessment of Pharmacokinetic Profile of the Patches by Measuring Time of Maximum Plasma Nicotine Concentration (tmax)

Timeframe: Predose (within 1 hour before dosing), 0.5, 1, 2, 3, 4,5, 6, 8, 10, 12, 14, 16, 18, 20, 24, 25, 26, 27, 28, 30, 32, and 36 hours postdose in each treatment period

Assessment of Pharmacokinetic Profile of the Patches by Measuring Elimination Half-Life (t1/2)

Timeframe: Predose (within 1 hour before dosing), 0.5, 1, 2, 3, 4,5, 6, 8, 10, 12, 14, 16, 18, 20, 24, 25, 26, 27, 28, 30, 32, and 36 hours postdose in each treatment period

Mean Adhesion Score

Timeframe: 0, 6, 12, 18 and 24 hours post-dose

Interventions:
Drug: NicoDerm CQ patch (GSK Dungarvan)
Drug: NicoDerm CQ (Alza)
Enrollment:
22
Observational study model:
Not applicable
Primary completion date:
2021-25-10
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Tobacco Use Disorder
Product
nicotine
Collaborators
Not applicable
Study date(s)
September 2021 to October 2021
Type
Interventional
Phase
1

Participation criteria

Sex
Female & Male
Age
21 - 55 Years
Accepts healthy volunteers
Yes
  • Participant provision of a signed and dated informed consent document indicating that the participant has been informed of all pertinent aspects of the study before any assessment is performed.
  • Participant is willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
  • A participant who is an employee of the investigational site, either directly involved in the conduct of the study or a member of their immediate family; or an employee of the
  • investigational site otherwise supervised by the investigator; or, a GSK Consumer Health (CH) employee directly involved in the conduct of the study or a member of their immediate family.
Inclusion and exclusion criteria
Inclusion criteria:
  • Participant provision of a signed and dated informed consent document indicating that the participant has been informed of all pertinent aspects of the study before any assessment is performed.
  • Participant is willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
  • A participant in good general and mental health with, in the opinion of the investigator or medically qualified designee, as determined by medical evaluation, including a detailed medical history, full physical examination, including blood pressure and pulse rate measurement, 12-lead Electrocardiogram (ECG) or clinical laboratory tests.
  • Body Mass Index (BMI) of 19 to 27 kilogram/meter Squared (kg/m^2); and a total body weight >50 kg (110 Pound-Mass [lbs]).
  • Any female participant of childbearing potential and at risk for pregnancy must agree to use a highly effective method of contraception throughout the study and for at least 5 days after the last dose of assigned treatment. Female participant who are not of childbearing potential must meet requirements of protocol.
  • Participants admits to having smoked more than 10 cigarettes per day for the preceding one year (prior to initial dose).
  • Participant with two negative tests (one at screening and one at check in Day-2) for active COVID-19, separated by > 24 hours.
Exclusion criteria:
  • A participant who is an employee of the investigational site, either directly involved in the conduct of the study or a member of their immediate family; or an employee of the investigational site otherwise supervised by the investigator; or, a GSK Consumer Health (CH) employee directly involved in the conduct of the study or a member of their immediate family.
  • A participant who has participated in other studies (including non-medicinal studies) involving any investigational product(s) within 30 days before first dosing.
  • A participant with, in the opinion of the investigator or medically qualified designee, an acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator or medically qualified designee, would make the participant inappropriate for entry into this study.
  • A Participant who is pregnant as confirmed by a positive serum pregnancy test or intending to become pregnant over the duration of the study.
  • A participant who is breastfeeding.
  • A participant with known or suspected intolerance or hypersensitivity to the study materials (or closely related compounds) or any of their stated ingredients ethylene vinyl acetatecopolymer, polyisobutylene and high density polyethylene.
  • Diagnosis of long QT syndrome or corrected QT (QTc) > 450 Millisecond (msec) for a male participant and > 470 msec for a female participant at screening.
  • A participant unwilling or unable to comply with Lifestyle Considerations described in this protocol.
  • Participant is unwilling to abstain from tobacco or nicotine-containing product use during the study (from check-in to the completion of the last pharmacokinetics (PK) blood sampling). Expired carbon monoxide (CO) measurement immediately prior to randomization (first treatment session) and dosing (second treatment session) should be less than or equal to (<=) 10 parts per million (ppm) for the participant to be dosed.
  • Participant has used chewing tobacco, tobacco products or electronic cigarettes other than cigarettes within 21 days of Visit 1.

    • Use of any medication (including over-the-counter medications and herbal remedies) within 2 weeks before first scheduled study drug administration or within < 10 times the elimination half-life of the respective drug (whichever is longer), or is anticipated to require any concomitant medication during that period or at any time throughout the study. Allowed treatments are:

    • systemic contraceptives and hormone replacement therapy, as long as female participant is on stable treatment for at least 3 months and continues treatment throughout the study.
  • Evidence or history of clinically significant laboratory abnormality, hematological, renal, endocrine, pulmonary, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease within the last 5 years that may increase the risk associated with study participation, as assessed by the Investigator or medically qualified designee.
  • A participant with a positive urine drug screen, for Tetrahydrocannabinol (THC), amphetamine, cocaine, 3,4- methylenedioxy-N-methylamphetamine (MDMA)/ecstasy, methamphetamine, or opiates.
  • Clinically relevant chronic or acute infectious illnesses or febrile infections within two weeks prior to start of the study.
  • participant with signs and symptoms suggestive of COVID-19 (i.e. fever, cough, etc) within 14 days of inpatient admission.
  • Participant with known COVID-19 positive contacts in the past 14 days.
  • Presence of tattoo, excessive hair (including shaved hair) or scarring on the test site on the back which in the opinion of the investigator would interfere with the study assessments.

    • Participant who currently in the opinion of the investigator, after medical review, has any of the following conditions:

    • Thrombophlebitis, thromboembolic disorders
    • A history of deep vein thrombophlebitis or thromboembolic disorders
    • Cerebrovascular or coronary artery disease (current or history)
    • Valvular heart disease with complications
    • Severe hypertension
    • Diabetes with vascular involvement
    • Headaches with focal neurological symptoms
    • Major surgery with prolonged immobilization.
  • Surgical procedures or use of topical pharmacologic treatments directly over the test site(s) within 90 days before enrollment.

    • A participant with any condition possibly affecting drug absorption, distribution, metabolism or excretion of any drug substance but not limited to any of the following:

    • History or current evidence of dermatologic disorders/skin diseases including sunburn and keloids, that may interfere with the transdermal absorption of the study drug(s) at the test site;
    • History or current evidence of renal disease or impaired renal function at screening as indicated by abnormal levels of serum creatinine (>=1.4 milligram per deciliter [mg/dL]) or Blood urea nitrogen (BUN) (>=25 mg/dL) or the presence of clinically significant abnormal urinary constituents (e.g. albuminuria);
    • History or current evidence of ongoing hepatic disease or impaired hepatic function at screening. A candidate will be excluded if more than one of the following lab value deviations are found: 1) Aspartate transaminase/Serum glutamic oxaloacetic transaminase (AST/SGOT) (>= 1.2 upper limit of normal [ULN]), Alanine transaminase/Serum glutamic pyruvic transaminase (ALT/SGPT) (>= 1.2 ULN), 2) Gamma glutamyl transpeptidase (GGT) (>= 1.2 ULN), Alkaline phosphatase (ALP) (>= 1.2 ULN), 3) bilirubin (>= 1.0 mg/dL) or Creatine kinase (CK) (>= 3 to 5 ULN). A single deviation from the above values is acceptable and will not exclude the candidate, unless specifically advised by the Investigator;
    • Evidence of urinary obstruction or difficulty in voiding at screening.
  • Evidence, as reported by analcohol breath testing during screening, for current alcohol abuse or reports a regular average alcohol consumption exceeding 18 gram (g) (women) or 35 g (men) of pure alcohol per day, i.e., 1 drink/day for women or 2 drinks/day for men (1 drink = 5 ounce (oz) of wine or 12 oz of beer or 1.5 oz of hard liquor) within 6 months of screening.
  • participant reported regular consumption of > 5 cups of coffee or tea per day (or equivalent consumption of >= 500 mg xanthine per day using other products).
  • Participant reports consumption of any drug metabolizing enzyme (e.g., CYP3A4 or other cytochrome P450 enzymes) inducing or inhibiting aliments, beverages or food supplements (e.g., broccoli, Brussels sprouts, grapefruit, grapefruit juice, star fruit, St. John’s Wort etc.) within 2 weeks prior to dosing.
  • Positive results at screening in any of the virology tests for human immunodeficiency virus-Ab (HIV-ab), hepatitis C virus-Ab (HCV-Ab), Hepatitis B surface antigen (HBsAg) and Hepatitis B Core Antibody (HBc-Ab) (Immunoglobulin G [IgG] + Immunoglobulin M [IgM]).
  • Performance of unaccustomed strenuous physical exercise (body building, high performance sports) from 2 weeks prior todosing.
  • Allergy to skin disinfecting agents, tape, or latex rubber, whenever appropriate substitutions cannot be applied or in the Investigator’s opinion may pose a risk to the candidate.
  • A participant who, in the opinion of the investigator or medically qualified designee, should not participate in the study.
  • Participation in a clinical trial with at least 470ml blood drawn, or blood donation within 30 days prior to the start of the study.
  • Hemoglobin value <11.0 g/dL
  • Participants who have previously been enrolled in this study.

Trial location(s)

Location
Status
Contact us
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Location
GSK Investigational Site
Springfield, Missouri, United States, 65802
Status
Study Complete
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Study documents

No study documents available.

Results overview

Study Results yet to be posted

Recruitment status
Completed
Actual primary completion date
2021-25-10
Actual study completion date
2021-25-10

Plain language summaries

Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.

Additional information about the trial

Additional information
Not applicable
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