Effect of Switching From Cigarette Smoking to THS on Systemic Endothelial Function in Subjects With Established Atherosclerotic Disease

NCT ID: NCT05566678

Last Updated: 2024-11-18

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-03-15
• Study Completion Date: 2023-03-31

Brief Summary

The purpose of this study is to demonstrate improvement in flow mediated dilation (FMD), a functional endpoint associated with the progression of atherosclerosis, when switching from cigarettes to the Tobacco Heating System (THS) in subjects with peripheral arterial disease (PAD) and/or coronary artery disease (CAD). The study is planned to be conducted in the US, Europe, and Asia.

Detailed Description

The goal of this longitudinal study is to demonstrate improvement in FMD, a functional endpoint associated with the progression of atherosclerosis and a predictor of future cardiovascular (CV) events in subjects with PAD and/or CAD, when switching from cigarettes to THS. Other CV functional endpoints, or cardiovascular biomarkers of potential harm (BoPH) representative of different pathophysiologic pathways associated with increased CV risk in smokers with established atherosclerosis will be assessed. It is expected that the totality of the evidence from this study will show the potential of THS to slow down the progression of atherosclerosis, thus helping to delay a CV event, or delaying a secondary event.

Conditions

Cardiovascular Diseases; Smoking; Tobacco Use; Peripheral Arterial Disease; Coronary Artery Disease

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Cigarette

Smokers who self-selected to continue smoking cigarettes.

Group Type: ACTIVE_COMPARATOR

Cigarette

Intervention Type: OTHER

Subjects who self-selected to continue smoking their own preferred brand of commercially available cigarettes.

Tobacco Heating System

Smokers who self-selected to switch to THS use.

Group Type: ACTIVE_COMPARATOR

THS

Intervention Type: OTHER

Subjects who self-selected to quit smoking during the study duration will switch from cigarettes to using THS.

Smoking Abstinence

Smokers who self-selected to abstain from smoking.

Group Type: ACTIVE_COMPARATOR

Smoking Abstinence

Intervention Type: OTHER

Subjects who self-selected to quit smoking may be prescribed Nicotine Replacement Therapy (NRT) to support them in remaining abstinent from use of any tobacco and nicotine containing products during the study. (Behavioral support will be provided to subjects to aid with abstinence.)

Interventions

Cigarette

Subjects who self-selected to continue smoking their own preferred brand of commercially available cigarettes.

Intervention Type: OTHER

THS

Subjects who self-selected to quit smoking during the study duration will switch from cigarettes to using THS.

Intervention Type: OTHER

Smoking Abstinence

Subjects who self-selected to quit smoking may be prescribed Nicotine Replacement Therapy (NRT) to support them in remaining abstinent from use of any tobacco and nicotine containing products during the study. (Behavioral support will be provided to subjects to aid with abstinence.)

Intervention Type: OTHER

Other Intervention Names

Tobacco Heating System 3.0

Eligibility Criteria

Inclusion Criteria

• History of coronary artery disease, defined as documented CAD (stable) with coronary artery stenosis on coronary angiogram ≥50% (incl. Percutaneous Coronary Intervention (PCI) / Coronary artery bypass graft surgery (CABG)) in the medical history or previously documented acute coronary syndrome (ACS) / myocardial infarction occurring more than 1 month prior to V1. AND / OR, History of peripheral artery disease (PAD) defined as ABI <0.9 or TBI <0.6 or clinical diagnosis of chronic, symptomatic lower limb ischemia as defined by Fontaine's stages I, IIa and IIb.
• Body mass index (BMI) 17.6-40.0 kg/m2 and body weight > 50 kg (male) or 40 kg (female).
• Subject has a smoking history of at least 10 years.
• Subject has not used other tobacco and nicotine products apart from cigarettes on a daily basis over the past year prior to V1.
• Subject has been smoking ≥ 10 commercially available cigarettes/day on average (no brand restriction) for at least 1 year prior to V1 (based on self-reporting).
• For subjects not willing to quit smoking only: have been advised to quit smoking and informed of smoking risks and of cessation programs and is still not willing to quit during the study duration.
• Subjects willing to quit smoking only: willing to and set a target quit date (TQD) within the next 28 days at V1 as assessed by self-reported questions

Exclusion Criteria

• Planned peripheral or coronary intervention or surgical procedure.
• Unstable angina pectoris.
• Critical limb ischemia (absolute peripheral pressures <50mmHg).
• Recent (< 30 days) PAD revascularization therapy prior to V1.
• Recent ACS / myocardial infarction or stroke / TIA <30 days prior to V1.
• Pre-existing symptomatic heart failure with reduced ejection fraction (EF<35%).
• Planned peripheral or coronary intervention or surgical procedure related to CAD or PAD.
• Subjects with spirometry values indicating chronic obstructive pulmonary disease (COPD) GOLD* Stage 3 or 4 (FEV1/FVC <0.7 & FEV1 <50% predicted [post-BD])
• Existing known serious infection or chronic inflammatory systemic disease (e.g., rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, uncontrolled diabetes (HbA1c ≥ 7.0 % [or ≥ 53.0 mmol/mol]) or uncontrolled hypertension (systolic blood pressure≥140 mmHg and / or diastolic blood pressure ≥90 mmHg., stage 4 and 5 chronic kidney disease, etc…).
• Currently active cancer or history of cancer within the last 5 years prior to V1.
• History of alcohol and / or drug abuse (other than tetrahydrocannabinol [THC]).
• Positive serology test (human immunodeficiency virus (HIV) 1/2), hepatitis B and / or C).
• Female subject is pregnant or breastfeeding, (a urine pregnancy test will be performed at V1 and V2)
• Previous participation in this study, or participation in an investigational study (drug or medical device) within 4 weeks before V1 (participation in observational studies/registries allowed)
• For women of childbearing potential, female subject who does not agree to using an acceptable method of effective contraception during the entire study.

[*Global Initiative for Obstructive Lung Disease]

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Philip Morris Products S.A.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Christelle Haziza, PhD

Role: STUDY_CHAIR

Philip Morris Products S.A.

Other Identifiers

P1-CVD-05

Identifier Type: -

Identifier Source: org_study_id