Nicotine Pharmacokinetics and Subjective Effects of Nicotine Pouch 1.0 Compared to Velo® Ice Cool and Zyn® Cool Mint Mini Dry in Healthy Smokers

Sponsor
Philip Morris Products S.A. (Industry)
Overall Status
Active, not recruiting
CT.gov ID
NCT05317195
Collaborator
(none)
24
1
6
4.4
5.5

Study Details

Study Description

Brief Summary

This is a single-center, randomized, controlled, open-label, cross-over study in healthy smoking subjects to investigate the nicotine pharmacokinetic (PK) profiles of 4 variants of Nicotine pouch 1.0 compared to marketed Velo - Nicotine Pouch (NP) and Zyn-NP. In addition, pharmacodynamic (PD) effects will be evaluated to provide further insights on Nicotine pouch 1.0 product acceptance and abuse liability. The study will be conducted with 3 periods and 6 sequences in a Williams design (cross-over).

Condition or Disease Intervention/Treatment Phase
  • Other: NP-1
  • Other: NP-2
  • Other: NP-3
  • Other: NP-4
  • Other: Velo-NP
  • Other: Zyn-NP
N/A

Detailed Description

The purpose of the study is to evaluate the nicotine PK profiles of 4 variants of NP 1.0 versus Velo-NP and Zyn-NP following a 30-minute use period. In addition, PD, including subjective effects and related behavioral assessments will be evaluated, to provide further insights on NP 1.0 product acceptance and abuse liability. Safety will be assessed throughout the study.

The aim is to evaluate if NP 1.0 can provide an acceptable alternative to smoking cigarettes in terms of both, nicotine delivery and sensorial satisfaction for smokers who would otherwise continue smoking cigarettes.

Study Design

Study Type:
Interventional
Actual Enrollment :
24 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Basic Science
Official Title:
A Single-center, Randomized, Controlled, Open-label Study to Investigate the Nicotine Pharmacokinetic Profiles and Subjective Effects of Four Variants of Nicotine Pouch 1.0 Compared to Velo® Ice Cool and Zyn® Cool Mint Mini Dry in Healthy Smokers
Actual Study Start Date :
Mar 15, 2022
Actual Primary Completion Date :
May 7, 2022
Anticipated Study Completion Date :
Jul 27, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: NP-1

Nicotine Pouch 1.0 (variant NP-1)

Other: NP-1
NP-1; 8.4 mg nicotine; pH 8.0; moisture 30

Other: NP-2
NP-2; 8.4 mg nicotine; pH 9.0; moisture 30

Other: NP-3
NP-3; 3.6 mg nicotine; pH 8.0; moisture 15

Other: NP-4
NP-4; 3.6 mg nicotine; pH 8.0; moisture 30

Other: Velo-NP
Velo-NP; 10 mg nicotine;

Other: Zyn-NP
Zyn-NP; 3 mg nicotine;

Experimental: NP-2

Nicotine Pouch 1.0 (variant NP-2)

Other: NP-1
NP-1; 8.4 mg nicotine; pH 8.0; moisture 30

Other: NP-2
NP-2; 8.4 mg nicotine; pH 9.0; moisture 30

Other: NP-3
NP-3; 3.6 mg nicotine; pH 8.0; moisture 15

Other: NP-4
NP-4; 3.6 mg nicotine; pH 8.0; moisture 30

Other: Velo-NP
Velo-NP; 10 mg nicotine;

Other: Zyn-NP
Zyn-NP; 3 mg nicotine;

Experimental: NP-3

Nicotine Pouch 1.0 (variant NP-3)

Other: NP-1
NP-1; 8.4 mg nicotine; pH 8.0; moisture 30

Other: NP-2
NP-2; 8.4 mg nicotine; pH 9.0; moisture 30

Other: NP-3
NP-3; 3.6 mg nicotine; pH 8.0; moisture 15

Other: NP-4
NP-4; 3.6 mg nicotine; pH 8.0; moisture 30

Other: Velo-NP
Velo-NP; 10 mg nicotine;

Other: Zyn-NP
Zyn-NP; 3 mg nicotine;

Experimental: NP-4

Nicotine Pouch 1.0 (variant NP-4)

Other: NP-1
NP-1; 8.4 mg nicotine; pH 8.0; moisture 30

Other: NP-2
NP-2; 8.4 mg nicotine; pH 9.0; moisture 30

Other: NP-3
NP-3; 3.6 mg nicotine; pH 8.0; moisture 15

Other: NP-4
NP-4; 3.6 mg nicotine; pH 8.0; moisture 30

Other: Velo-NP
Velo-NP; 10 mg nicotine;

Other: Zyn-NP
Zyn-NP; 3 mg nicotine;

Active Comparator: Velo-NP

Velo® Ice Cool

Other: NP-1
NP-1; 8.4 mg nicotine; pH 8.0; moisture 30

Other: NP-2
NP-2; 8.4 mg nicotine; pH 9.0; moisture 30

Other: NP-3
NP-3; 3.6 mg nicotine; pH 8.0; moisture 15

Other: NP-4
NP-4; 3.6 mg nicotine; pH 8.0; moisture 30

Other: Velo-NP
Velo-NP; 10 mg nicotine;

Other: Zyn-NP
Zyn-NP; 3 mg nicotine;

Active Comparator: Zyn-NP

Zyn® Cool Mint Mini Dry

Other: NP-1
NP-1; 8.4 mg nicotine; pH 8.0; moisture 30

Other: NP-2
NP-2; 8.4 mg nicotine; pH 9.0; moisture 30

Other: NP-3
NP-3; 3.6 mg nicotine; pH 8.0; moisture 15

Other: NP-4
NP-4; 3.6 mg nicotine; pH 8.0; moisture 30

Other: Velo-NP
Velo-NP; 10 mg nicotine;

Other: Zyn-NP
Zyn-NP; 3 mg nicotine;

Outcome Measures

Primary Outcome Measures

  1. Background-corrected maximum plasma concentration [Cmax] [Measured at baseline (day 1), day 2, and day 3]

    To measure the background-corrected maximum plasma concentration [Cmax] of 4 variants of NP 1.0 nicotine pouches compared to Velo-NP and Zyn-NP in healthy smokers from a 30 minutes product use period.

  2. Background-corrected time to the maximum concentration [Tmax] [Measured at baseline (day 1), day 2, and day 3]

    To measure the background-corrected time to the maximum concentration [Tmax] of 4 variants of NP 1.0 nicotine pouches compared to Velo-NP and Zyn-NP in healthy smokers from a 30 minutes product use period.

  3. Area under the background-corrected concentration-time curve (AUC) from start of product use [Measured at baseline (day 1), day 2, and day 3]

    To measure the area under the background-corrected concentration-time curve (AUC) from start of product use of 4 variants of NP 1.0 nicotine pouches compared to Velo-NP and Zyn-NP in healthy smokers from a 30 minutes product use period.

Secondary Outcome Measures

  1. Score of cigarette craving by the visual analog sale (VAS)-craving assessment [Measured at baseline (day 1), day 2, and day 3]

    To measure cigarette craving by the visual analog sale (VAS)-craving assessment in healthy smokers following a 30 minutes product use period of 4 variants of Nicotine pouch 1.0 compared to Velo-NP and Zyn-NP.

  2. Score of "in the moment" product liking by the VAS-liking assessment [Measured at baseline (day 1), day 2, and day 3]

    To measure "in the moment" product liking by the VAS-liking assessment in healthy smokers following a 30 minutes product use period of 4 variants of Nicotine pouch 1.0 compared to Velo-NP and Zyn-NP.

  3. Score of overall product liking by the VAS-liking assessment [Measured at baseline (day 1), day 2, and day 3]

    To measure overall product liking by the VAS-liking assessment in healthy smokers following a 30 minutes product use period of 4 variants of Nicotine pouch 1.0 compared to Velo-NP and Zyn-NP.

  4. Score of product satisfaction by the VAS-satisfaction assessment [Measured at baseline (day 1), day 2, and day 3]

    To measure product satisfaction by the VAS-satisfaction assessment in healthy smokers following a 30 minutes product use period of 4 variants of Nicotine pouch 1.0 compared to Velo-NP and Zyn-NP.

  5. Score of product intention to use again by the VAS-intention to use again assessment [Measured at baseline (day 1), day 2, and day 3]

    To measure intention to use product again by the VAS-intention to use again assessment in healthy smokers following a 30 minutes product use period of 4 variants of Nicotine pouch 1.0 compared to Velo-NP and Zyn-NP.

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Main Inclusion Criteria:
  • Subject has smoked continuously for at least the last 3 years prior to the Screening visit.

  • Subject has smoked ≥ 10 commercially available cigarettes per day for 4 weeks prior to Screening Visit and Admission. Smoking status will be verified based on a urinary cotinine test (cotinine ≥ 500 ng/mL).

  • Subject does not plan to quit using tobacco and/or nicotine products within the next 3 months.

  • Smoking, healthy subject as judged by the Investigator or designee based on available assessments from the Screening period.

Main Exclusion Criteria:
  • As per the Investigator's judgment, the subject cannot participate in the study for any reason other than medical.

  • Subject is legally incompetent, or physically or mentally incapable of giving consent.

  • Subject has a clinically relevant disease that requires medication, which as per the judgment of the Investigator would jeopardize the safety of the subject.

  • Subject has donated or received whole blood or blood products within 30 days prior to Screening Visit.

  • Subject has a BMI < 18.5 kg/m2 or > 32.0 kg/m2 (Europe) or > 35.0 kg/m2 (USA).

  • For women only: subject is pregnant (does not have negative pregnancy test at Screening Visit and at Admission) or is breastfeeding.

Contacts and Locations

Locations

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

Sponsors and Collaborators

  • Philip Morris Products S.A.

Investigators

  • Principal Investigator: Rajkumar Chetty, MD, Celerion

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Philip Morris Products S.A.
ClinicalTrials.gov Identifier:
NCT05317195
Other Study ID Numbers:
  • P5-PK-01-EXP
First Posted:
Apr 7, 2022
Last Update Posted:
Jul 6, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Philip Morris Products S.A.

Study Results

No Results Posted as of Jul 6, 2022