CSD190401: A Study to Assess Elements of Abuse Liability for Nicotine-containing Pouch Tobacco Products
NCT ID: NCT04372290
Last Updated: 2020-09-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
42 participants
INTERVENTIONAL
2020-05-06
2020-06-04
Brief Summary
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Detailed Description
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Potential subjects may complete a pre-Screening telephone interview and will complete a Screening Visit to assess their eligibility within 45 days prior to check-in and enrollment/randomization.
Starting on Day -1, eligible subjects will begin confinement at the clinical site for 6 days. Subjects will be randomized to evaluate one investigational product (IP) in each of five separate Test Sessions, such that each subject will evaluate five IPs, including three strengths of the nicotine pouches, and both a high- and a low-AL comparator.
Each Test Session will last for approximately 4 hours during and following IP use and will include collection of both PD measures (subjective and physiological) and PK measures.
On Day -1, subjects will participate in an IP acclimation period where they will be instructed on how to use the nicotine pouch IP and the nicotine gum (low-AL comparator IP). At the end of the acclimation period, subjects will have access to their usual brand (UB) cigarettes for ad libitum use until the 12-hour tobacco abstinence begins prior to the Day 1 Test Session.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
OTHER
NONE
Study Groups
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Product usage order ABECD
Subjects will use each of the 5 products sequentially (ABECD) during an evaluation period, followed by a 6 hour Test Session.
Product A
Usual brand (UB) filtered, combustible cigarette
Product B
Nicorette® White Ice Mint 2 mg nicotine gum
Product C
CSD1904-01, a nicotine pouch, 2 mg nicotine
Product D
CSD1904-02, a nicotine pouch, 4 mg nicotine
Product E
CSD1904-02, a nicotine pouch, 8 mg nicotine (simultaneous use of two 4 mg nicotine pouches)
Product usage order BCADE
Subjects will use each of the 5 products sequentially (BCADE) during an evaluation period, followed by a 6 hour Test Session.
Product A
Usual brand (UB) filtered, combustible cigarette
Product B
Nicorette® White Ice Mint 2 mg nicotine gum
Product C
CSD1904-01, a nicotine pouch, 2 mg nicotine
Product D
CSD1904-02, a nicotine pouch, 4 mg nicotine
Product E
CSD1904-02, a nicotine pouch, 8 mg nicotine (simultaneous use of two 4 mg nicotine pouches)
Product usage order CDBEA
Subjects will use each of the 5 products sequentially (CDBEA) during an evaluation period, followed by a 6 hour Test Session.
Product A
Usual brand (UB) filtered, combustible cigarette
Product B
Nicorette® White Ice Mint 2 mg nicotine gum
Product C
CSD1904-01, a nicotine pouch, 2 mg nicotine
Product D
CSD1904-02, a nicotine pouch, 4 mg nicotine
Product E
CSD1904-02, a nicotine pouch, 8 mg nicotine (simultaneous use of two 4 mg nicotine pouches)
Product usage order DECAB
Subjects will use each of the 5 products sequentially (DECAB) during an evaluation period, followed by a 6 hour Test Session.
Product A
Usual brand (UB) filtered, combustible cigarette
Product B
Nicorette® White Ice Mint 2 mg nicotine gum
Product C
CSD1904-01, a nicotine pouch, 2 mg nicotine
Product D
CSD1904-02, a nicotine pouch, 4 mg nicotine
Product E
CSD1904-02, a nicotine pouch, 8 mg nicotine (simultaneous use of two 4 mg nicotine pouches)
Product usage order EADBC
Subjects will use each of the 5 products sequentially (EADBC) during an evaluation period, followed by a 6 hour Test Session.
Product A
Usual brand (UB) filtered, combustible cigarette
Product B
Nicorette® White Ice Mint 2 mg nicotine gum
Product C
CSD1904-01, a nicotine pouch, 2 mg nicotine
Product D
CSD1904-02, a nicotine pouch, 4 mg nicotine
Product E
CSD1904-02, a nicotine pouch, 8 mg nicotine (simultaneous use of two 4 mg nicotine pouches)
Product usage order DCEBA
Subjects will use each of the 5 products sequentially (DCEBA) during an evaluation period, followed by a 6 hour Test Session.
Product A
Usual brand (UB) filtered, combustible cigarette
Product B
Nicorette® White Ice Mint 2 mg nicotine gum
Product C
CSD1904-01, a nicotine pouch, 2 mg nicotine
Product D
CSD1904-02, a nicotine pouch, 4 mg nicotine
Product E
CSD1904-02, a nicotine pouch, 8 mg nicotine (simultaneous use of two 4 mg nicotine pouches)
Product usage order EDACB
Subjects will use each of the 5 products sequentially (EDACB) during an evaluation period, followed by a 6 hour Test Session.
Product A
Usual brand (UB) filtered, combustible cigarette
Product B
Nicorette® White Ice Mint 2 mg nicotine gum
Product C
CSD1904-01, a nicotine pouch, 2 mg nicotine
Product D
CSD1904-02, a nicotine pouch, 4 mg nicotine
Product E
CSD1904-02, a nicotine pouch, 8 mg nicotine (simultaneous use of two 4 mg nicotine pouches)
Product usage order AEBDC
Subjects will use each of the 5 products sequentially (AEBDC) during an evaluation period, followed by a 6 hour Test Session.
Product A
Usual brand (UB) filtered, combustible cigarette
Product B
Nicorette® White Ice Mint 2 mg nicotine gum
Product C
CSD1904-01, a nicotine pouch, 2 mg nicotine
Product D
CSD1904-02, a nicotine pouch, 4 mg nicotine
Product E
CSD1904-02, a nicotine pouch, 8 mg nicotine (simultaneous use of two 4 mg nicotine pouches)
Product usage order BACED
Subjects will use each of the 5 products sequentially (BACED) during an evaluation period, followed by a 6 hour Test Session.
Product A
Usual brand (UB) filtered, combustible cigarette
Product B
Nicorette® White Ice Mint 2 mg nicotine gum
Product C
CSD1904-01, a nicotine pouch, 2 mg nicotine
Product D
CSD1904-02, a nicotine pouch, 4 mg nicotine
Product E
CSD1904-02, a nicotine pouch, 8 mg nicotine (simultaneous use of two 4 mg nicotine pouches)
Product usage order CBDAE
Subjects will use each of the 5 products sequentially (CBDAE) during an evaluation period, followed by a 6 hour Test Session.
Product A
Usual brand (UB) filtered, combustible cigarette
Product B
Nicorette® White Ice Mint 2 mg nicotine gum
Product C
CSD1904-01, a nicotine pouch, 2 mg nicotine
Product D
CSD1904-02, a nicotine pouch, 4 mg nicotine
Product E
CSD1904-02, a nicotine pouch, 8 mg nicotine (simultaneous use of two 4 mg nicotine pouches)
Interventions
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Product A
Usual brand (UB) filtered, combustible cigarette
Product B
Nicorette® White Ice Mint 2 mg nicotine gum
Product C
CSD1904-01, a nicotine pouch, 2 mg nicotine
Product D
CSD1904-02, a nicotine pouch, 4 mg nicotine
Product E
CSD1904-02, a nicotine pouch, 8 mg nicotine (simultaneous use of two 4 mg nicotine pouches)
Eligibility Criteria
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Inclusion Criteria
2. Generally healthy male or female, 21 to 60 years of age, inclusive, at the time of consent.
3. Expired breath carbon monoxide level is ≥ 10 ppm and ≤ 100 ppm at Screening.
4. Positive urine cotinine test at Screening.
5. Smokes combustible, filtered, non-menthol or menthol cigarettes, 83 mm to 100 mm in length as primary source of tobacco. Other cigarette sizes may be allowed with sponsor approval.
6. Smokers who also use smokeless tobacco products may be enrolled.
7. Agrees to smoke same UB cigarette throughout the study period. UB cigarette is defined as the reported cigarette brand style currently smoked most frequently by the subject.
8. Smokes at least 10 cigarettes per day (on average) and inhales the smoke, for at least 6 months prior to Screening.
9. Response at Screening to Fagerström Test for Nicotine Dependence (FTND) Question 1 ("How soon after you wake up do you smoke your first cigarette?") is either "Within 5 minutes" or "6-30 minutes."
10. Willing to use UB cigarette, nicotine pouch products, and Nicorette gum during the study period.
11. Willing to abstain from tobacco and nicotine use for at least 12 hours prior to each Test Session.
12. Females must be willing to use a form of contraception acceptable to the Principal Investigator (PI) from the time of signing informed consent until End-of-Study.
13. Agrees to in-clinic confinement of 6 days (5 nights).
Exclusion Criteria
2. Presence of clinically significant uncontrolled cardiovascular, pulmonary, renal, hepatic, endocrine, gastrointestinal, psychiatric, hematological, neurological disease, or any other concurrent disease or medical condition that, in the opinion of the PI, makes the study subject unsuitable to participate in this clinical study.
3. History, presence of, or clinical laboratory test results indicating diabetes.
4. Systolic blood pressure of \> 160 mmHg or a diastolic blood pressure of \> 95 mmHg, measured after being seated for five minutes at Screening and at Day -1.
5. Weight of ≤ 110 pounds.
6. Hemoglobin level is \< 12.5 g/dL for females or \<13.0 g/dL for males at Screening.
7. Scheduled treatment for asthma currently or within the past consecutive 12 months prior to the Screening Visit. As-needed treatment, such as inhalers, may be included at the PI's discretion pending approval from the Medical Monitor.
8. Positive test for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C virus (HCV).
9. Any history of cancer, except for primary cancers of skin such as localized basal cell/squamous cell carcinoma that has been surgically and/or cryogenically removed.
10. Use of any medication or substance that aids in smoking cessation, including but not limited to any nicotine-replacement therapy (NRT) (e.g., nicotine gum, lozenge, patch), varenicline (Chantix®), bupropion (Wellbutrin®, Zyban®), or lobelia extract within (≤) 30 days prior to the signing of informed consent.
11. History or presence of bleeding or clotting disorders.
12. Any use of anticoagulants or aspirin (≥ 325 mg/day).
13. Whole blood donation within 8 weeks (≤ 56 days) prior to the signing of informed consent.
14. Plasma donation within (≤) 7 days prior to the signing of informed consent.
15. Participation in another clinical trial within (≤) 30 days prior to the signing of informed consent. The 30-day window for each subject will be derived from the date of the last study event in the previous study to the time of signing the informed consent form (ICF) in the current study.
16. Females who have a positive pregnancy test, are pregnant, breastfeeding, or intend to become pregnant during the course of the study.
17. Individuals ≥ 35 years of age currently using systemic, estrogen-containing contraception or hormone replacement therapy.
18. A positive urine drug screen without evidence of prescribed corresponding concomitant medication(s) at Screening or Day -1.
19. Postpones a decision to quit using tobacco- or nicotine-containing products in order to participate in this study or a previous attempt within (≤) 30 days prior to signing the ICF.
20. Drinks more than 21 servings of alcoholic beverages per week or has a positive alcohol screen result at Screening or Day -1.
21. Employed by a tobacco or nicotine company, the study site, or handles tobacco- or nicotine-containing products as part of their job.
22. Determined by the PI to be inappropriate for this study.
21 Years
60 Years
ALL
Yes
Sponsors
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RAI Services Company
INDUSTRY
Responsible Party
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Principal Investigators
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Bobbette Jones, DrPH
Role: STUDY_DIRECTOR
RAIS
Locations
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New Orleans Center for Clinical Research (NOCCR)
Knoxville, Tennessee, United States
Countries
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Other Identifiers
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CSD190401
Identifier Type: -
Identifier Source: org_study_id
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