Characterization of Product Use in Smokers Switching From Cigarettes to a RELX Electronic Nicotine Delivery System

Electronic Cigarette Use Clinical Trial

Official title:

A Randomized, Multi-Center, Open-Label, Parallel-Cohort Study to Characterize Product Use in Smokers Switching From Combustible Cigarettes to a RELX Electronic Nicotine Delivery System (ENDS)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04708106
• Other study ID #: RELX-003
• Status: Completed
• Phase: N/A
• Start date: October 15, 2020
• Est. completion date: July 7, 2021

Study information

• Verified date: July 2021
• Source: Cheerain HK Limited
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study will assess product use behaviors, biomarkers of exposure, subjective effects, and safety in smokers who switch to a RELX ENDS over 8-weeks.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 194
• Est. completion date: July 7, 2021
• Est. primary completion date: July 1, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 22 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Provides voluntary consent to participate in the study as documented on the signed informed consent form (ICF).

2. Is 22 to 65 years of age, inclusive, at the time of consent.

3. Is willing to comply with the requirements of the study.

4. Reports typically smoking 5 or more combustible CPD at Screening.

5. Has been a daily smoker for at least 12 months prior to Screening. Brief periods of non-smoking (e.g., up to ~7 consecutive days due to illness, trying to quit, participation in a study where smoking was prohibited) = 56 days prior to Screening will be permitted at the discretion of the Investigator.

6. Has a positive urine cotinine test (= 200 ng/mL) at Screening and Test Visit 1.

7. Has an exhaled carbon monoxide (ECO) value > 10 ppm at Screening and Test Visit 1.

8. Has daily access to a cell phone for daily product use reporting.

9. If female, meets one of the following criteria:

If of childbearing potential - agrees to use one of the accepted contraceptive regimens from at least 30 days prior to the first product use and during the study. An acceptable

method of contraception includes one of the following:

• Abstinence from heterosexual intercourse
• Hormonal contraceptives (birth control pills, injectable/implant/insertable hormonal birth control products, transdermal patch)
• Intrauterine device (with or without hormones) OR agrees to use a double barrier method (e.g. condom and spermicide) during the study. If a female of non-childbearing potential - should be surgically sterile (i.e. has undergone complete hysterectomy, bilateral oophorectomy, or tubal ligation) or in a menopausal state (at least 1 year without menses), as confirmed by follicle stimulating hormone (FSH) levels.

Exclusion Criteria:

1. Has a history or presence of clinically significant uncontrolled gastrointestinal, renal, hepatic, neurologic, hematologic, endocrine, oncologic, urologic, pulmonary, immunologic, psychiatric, or cardiovascular disease, or any other condition that, in the opinion of the Investigator, would jeopardize the safety of the subject or impact the validity of the study results.

2. Has a clinically significant abnormal finding on the physical examination, medical history, vital signs, electrocardiogram (ECG), or clinical laboratory results, in the opinion of the Investigator.

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

4. Has a positive COVID-19 test at Screening or during the study.

5. Has had an acute illness (e.g., upper respiratory infection, viral infection) within 14 days prior to Test Visit 1.

6. Has a fever (> 100.5°F) at Screening or Test Visit 1.

7. Has a body mass index (BMI) greater than 40.0 kg/m2 or less than 18.0 kg/m2 at Screening.

8. Has a systolic blood pressure < 90 mmHg or > 150 mmHg, diastolic blood pressure < 40 mmHg or > 95 mmHg, or heart rate < 40 bpm or > 99 bpm at Screening.

9. Has a post-bronchodilator forced expiratory volume in 1 second:forced vital capacity (FEV1:FVC) ratio < 0.7 and FEV1 < 50% of predicted at Screening.

10. Has a post-bronchodilator FEV1 increase = 12% and > 200 mL from pre- to post-bronchodilator at Screening.

11. Has used an ENDS product on >7 days during each of the 3 months prior to Screening or any use from Screening to Test Visit 1 other than as may be required for this study.

12. Reports use of a very-low nicotine content cigarette (e.g., Moonlight, Spectrum, VLN) as usual brand.

13. Has used nicotine-containing products other than manufactured cigarettes (e.g., ENDS products (e-cigarettes), roll-your-own cigarettes, bidis, snuff, nicotine inhaler, pipe, cigar, chewing tobacco, nicotine patch, nicotine spray, nicotine lozenge, or nicotine gum) within 14 days prior to Test Visit 1.

14. Has used any products for the purpose of smoking cessation, including, but not limited to, nicotine replacement therapies, varenicline (Chantix), or buproprion (Zyban) from 30 days prior to Screening through the duration of the study.

15. Is a self-reported puffer (i.e., draws smoke from the cigarette into the mouth and throat but does not inhale).

16. Is postponing a planned smoking quit attempt in order to participate in the study.

17. Has a history of drug or alcohol abuse within 12 months prior to Screening, as determined by the Investigator.

18. Is allergic to PG or glycerin.

19. Has a positive urine drug or alcohol breath test at Screening or Test Visit 1. At the discretion of the investigator, a subject testing positive for tetrahydrocannabinol may be permitted to participate if the subject reports use by routes other than inhalation.

20. If female, the subject is pregnant, breastfeeding, or intends to become pregnant from Screening through the duration of the study.

21. Has been treated for depression, diabetes, asthma, emphysema, or chronic obstructive pulmonary disease within 12 months prior to Test Visit 1.

22. Has previously been diagnosed with any form of cancer, except for basal cell or squamous epithelial carcinomas of the skin that have been resected at least 12 months prior to Screening 1.

23. Has a planned surgery that would occur during study participation.

24. Has participated in a previous clinical study for an investigational drug, device, biologic, or tobacco product within 30 days prior to Test Visit 1.

25. Is or has a first-degree relative (e.g., spouse, parent, sibling, or child) who is a current or former employee of a tobacco or ENDS manufacturer or is a named party or class representative in litigation with the tobacco or ENDS industry.

26. Is or has a first-degree relative (e.g., spouse, parent, sibling, or child) who is a current employee of the clinic site.

27. Is or has a first-degree relative (e.g., spouse, parent, sibling, or child) who is a current employee of the Sponsor.

28. Has previously taken part in (from completion of any baseline measurements), has been withdrawn from, or has completed this study.

29. In the opinion of the Investigator, the subject should not participate in this study.

Related Conditions & MeSH terms

• Electronic Cigarette Use

Intervention

Other:
• RELX ENDS Tobacco Flavor
Ad libitum use of the RELX ENDS Tobacco Flavor product
• RELX ENDS Menthol Flavor
Ad libitum use of the RELX ENDS Menthol product
• RELX ENDS Tobacco and Menthol Flavors
Ad libitum use of the RELX ENDS Tobacco and Menthol Flavor products

Locations

Country	Name	City	State
United States	Pillar Clinical Research	Bentonville	Arkansas
United States	AMR - Knoxville	Knoxville	Tennessee
United States	AMR - Las Vegas	Las Vegas	Nevada
United States	AMR - Lexington	Lexington	Kentucky
United States	QPS	Springfield	Missouri

Sponsors (1)

Lead Sponsor	Collaborator
Cheerain HK Limited

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Weekly RELX ENDS product use	Self-reported number of RELX ENDS pods started each week.	56 days
Primary	Daily number of cigarettes smoked	Self-reported number of cigarettes smoked daily by study week.	56 days
Primary	Number of puffs from the RELX ENDS each day	Self-reported number of puffs from the RELX ENDS daily by study week (0, < 100, = 100 per day).	56 days
Secondary	Biomarkers of exposure measured in blood	Change in carbon monoxide concentration in the blood.	Baseline, Day 28, and Day 56
Secondary	Biomarkers of tobacco exposure measured in urine	Change in creatinine-adjusted NNAL, NNN, 3-HPMA, CEMA, HMPMA, S-PMA, HEMA, 1-OHP, o-toluidine, nicotine equivalents, and propylene glycol excreted in urine.	Baseline, Day 28, and Day 56
Secondary	Subjective effects as measured by the Penn State [Electronic] Cigarette Dependence Index (PS[E]CDI)	Change in product dependence as measured by the PSCDI/PSECDI total score. Total scores may range for 0 to 20, with higher levels of dependence associated with higher scores.	Baseline, Day 14, Day 28, Day 42, and Day 56
Secondary	Subjective effects as measured by the Cough Questionnaire	Change in self-reported cough symptoms as measured by responses to the Cough Questionnaire.	Baseline, Day 14, Day 28, Day 42, and Day 56
Secondary	Subjective effects as measured by the Questionnaire of Smoking Urges-Brief (QSU-Brief)	Change in smoking urge as measured by the QSU-Brief factor 1 and factor 2 scores. Questionnaire responses are measured on a Likert scale range of 1 [not at all] to 7 [extremely].	Baseline, Day 14, Day 28, Day 42, and Day 56
Secondary	Subjective effects as measured by the Minnesota Tobacco Withdrawal Scale-Revised (MTWS-R)	Change in withdrawal symptoms as measured by the MTWS-R total score, which includes the DSM-5 and craving items from the Minnesota Tobacco Withdrawal Scale. Questionnaire responses are measured on a Likert scale range of 0 [none] to 4 [severe]).	Baseline, Day 14, Day 28, Day 42, and Day 56
Secondary	Subjective effects as measured by the Modified Product Evaluation Scale (mPES)	Change in product assessments as measured by mPES satisfaction, psychological reward, aversion, and relief subscale scores. Questionnaire responses are measured on a Likert scale range of 1 [not at all] to 7 [extremely].	Baseline, Day 14, Day 28, Day 42, and Day 56
Secondary	Subjective effects as measured by the Future Intent to Use Questionnaire	Change in future intent to use cigarettes and ENDS products as measured by responses to the Future Intent to Use Questionnaire. Questionnaire responses are measured on a Likert scale range of 1 [extremely unlikely] to 7 [extremely likely].	Baseline, Day 14, Day 28, Day 42, and Day 56
Secondary	Subjective Effects as measured by the Health Effects Perceptions Questionnaire	Harmful and addictiveness perceptions as measured by responses to the Health Effects Perceptions Questionnaire.	Baseline and Day 56
Secondary	Puff topography - number of puffs	Change in the number of puffs during a 1-hour puff topography session.	Baseline, Day 28, and Day 56
Secondary	Puff topography - puff duration	Change in puff duration during a 1-hour puff topography session.	Baseline, Day 28, and Day 56
Secondary	Puff topography - puff volume	Change in puff volume during a 1-hour puff topography session.	Baseline, Day 28, and Day 56
Secondary	Puff topography - peak puff flow rate	Change in peak puff flow rate during a 1-hour puff topography session.	Baseline, Day 28, and Day 56
Secondary	Puff topography - average flow rate	Change in average flow rate during a 1-hour puff topography session.	Baseline, Day 28, and Day 56
Secondary	Puff topography - inter-puff interval	Change in inter-puff interval during a 1-hour puff topography session.	Baseline, Day 28, and Day 56
Secondary	RELX ENDS product use	Change in pod weight during a 1-hour topography session	Day 28 and Day 56
Secondary	Incidence of product-use emergent adverse events [Safety and Tolerability]	Incidence of product-use emergent adverse events	56 days