A Randomised, Cross-Over, Nicotine Pharmacokinetic and Pharmacodynamic Study of Heated Tobacco Products Compared to Combustible Cigarettes

Sponsor
Imperial Brands PLC (Industry)
Overall Status
Completed
CT.gov ID
NCT05459857
Collaborator
(none)
24
1
4
2
12.2

Study Details

Study Description

Brief Summary

This is a randomised, cross-over, open-label, confinement study conducted in 24 adult male or female smokers of combustible cigarettes. The study investigates combustible and heated tobacco (HT) products in a cross-over design, including pharmacokinetic evaluation, subjective questionnaire assessments, as well as safety evaluation.

Subjects will perform a screening visit and a 5-day confinement period.

Condition or Disease Intervention/Treatment Phase
  • Other: Heated tobacco device Intense (Product A)
  • Other: Heated tobacco device Regular (Product B)
  • Other: Heated tobacco device Menthol (Product C)
  • Other: Combustible cigarette (Product D)
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
24 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
A Randomised, Cross-Over, Nicotine Pharmacokinetic and Pharmacodynamic Study of Heated Tobacco Products Compared to Combustible Cigarettes
Actual Study Start Date :
Oct 1, 2021
Actual Primary Completion Date :
Nov 30, 2021
Actual Study Completion Date :
Nov 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Product sequence ABCD

Subjects use Product A on Day 1, Product B on Day 2, Product C on Day 3 and Product D on Day 4

Other: Heated tobacco device Intense (Product A)
Heated Tobacco device Intense, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Other: Heated tobacco device Regular (Product B)
Heated Tobacco device Regular, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Other: Heated tobacco device Menthol (Product C)
Heated Tobacco device Menthol, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Other: Combustible cigarette (Product D)
Subject's own brand combustible cigarette, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Experimental: Product sequence BDAC

Subjects use Product B on Day 1, Product D on Day 2, Product A on Day 3 and Product C on Day 4

Other: Heated tobacco device Intense (Product A)
Heated Tobacco device Intense, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Other: Heated tobacco device Regular (Product B)
Heated Tobacco device Regular, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Other: Heated tobacco device Menthol (Product C)
Heated Tobacco device Menthol, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Other: Combustible cigarette (Product D)
Subject's own brand combustible cigarette, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Experimental: Product sequence CADB

Subjects use Product C on Day 1, Product A on Day 2, Product D on Day 3 and Product B on Day 4

Other: Heated tobacco device Intense (Product A)
Heated Tobacco device Intense, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Other: Heated tobacco device Regular (Product B)
Heated Tobacco device Regular, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Other: Heated tobacco device Menthol (Product C)
Heated Tobacco device Menthol, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Other: Combustible cigarette (Product D)
Subject's own brand combustible cigarette, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Experimental: Product sequence DCBA

Subjects use Product D on Day 1, Product C on Day 2, Product B on Day 3 and Product A on Day 4

Other: Heated tobacco device Intense (Product A)
Heated Tobacco device Intense, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Other: Heated tobacco device Regular (Product B)
Heated Tobacco device Regular, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Other: Heated tobacco device Menthol (Product C)
Heated Tobacco device Menthol, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Other: Combustible cigarette (Product D)
Subject's own brand combustible cigarette, used under controlled conditions (i.e., completely use a single unit of the product, with puffs taken at 30-second intervals and puffs 3 seconds in duration)

Outcome Measures

Primary Outcome Measures

  1. Nicotine Cmax [5 minutes pre-study product use and at 2, 4, 6, 8, 10, 15, 30, 45, 60, 120, and 240 minutes following the start of study product use]

    Maximum measured plasma nicotine concentration

  2. Nicotine AUCt [5 minutes pre-study product use and at 2, 4, 6, 8, 10, 15, 30, 45, 60, 120, and 240 minutes following the start of study product use]

    The area under the concentration time curve for nicotine, from time 0 to the last observed non-zero concentration

Secondary Outcome Measures

  1. Smoking urges Emax [10 minutes prior to the start of the product use session, and at 4, 8, 15, 45, 60, 210 and 240 following the start of study product use minutes]

    The maximum change from baseline Visual Analog Scale (VAS) score (VASpre-use - VASpost-use). Subjects answer the question "How strong is your urge to smoke right now?" on a VAS: from Not at all on the left (0%) to Extreme on the right (100%).

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Reports smoking an average of at least 10 manufactured combustible (menthol or non-menthol) cigarettes per day for at least 12 months prior to Screening

  • Has a positive urine cotinine (>500 ng/mL) at Screening

  • Has an exhaled carbon monoxide >10 ppm at Screening

  • A female subject of childbearing potential must use contraception

  • Male subject must use contraception

Exclusion Criteria:
  • Has a history or presence of clinically significant disease or condition that, in the opinion of the Investigator, would jeopardise the safety of the subject or impact the validity of the study results.

  • Has a positive test for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C virus (HCV) at Screening

  • Has a fever (>38.05°C) at Screening or check-in

  • Has a history or presence of drug or alcohol abuse within 24 months of Check-in

  • Pregnant or lactating females

  • Has used any prescription smoking cessation treatments within 3 months prior to Check-in

  • Is planning to quit smoking during the study or within the next 3 months

Contacts and Locations

Locations

Site City State Country Postal Code
1 Celerion Belfast Nothern Ireland United Kingdom BT9 6AD

Sponsors and Collaborators

  • Imperial Brands PLC

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Imperial Brands PLC
ClinicalTrials.gov Identifier:
NCT05459857
Other Study ID Numbers:
  • NER01/0004
First Posted:
Jul 15, 2022
Last Update Posted:
Jul 15, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 15, 2022