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WithdrawnNCT05566678Updated Nov 18, 2024

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

An interventional study of Cigarette and THS in Cardiovascular Diseases, Smoking and Tobacco Use, sponsored by Philip Morris Products S.A.. Withdrawn. Open to participants aged 40 Years to 70 Years. Per ClinicalTrials.gov, last updated 2024-11-18.

Sponsored by Philip Morris Products S.A. · Not applicable, Interventional, and Other

Why this study was withdrawn
The study was stopped before enrollment, after a feasibility review revealed we would be unable to measure the primary endpoint (flow mediated dilation - FMD) with a high degree of reproducibility and minimum variability in a multi-country setting.
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Non-randomized
Ages
40 Years to 70 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

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

Keywords

  • Flow Mediated Dilation
  • Atherosclerosis
03

In context

Cardiovascular Diseases

4,904 studies on the registry are indexed under Cardiovascular Diseases; 919 are open to participants now.

Browse Cardiovascular Diseases studies →

Lead sponsor

Philip Morris Products S.A. is the lead sponsor of 46 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
40 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Main 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

Main 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]

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Active comparator
    Cigarette

    Smokers who self-selected to continue smoking cigarettes.

    Other: Cigarette

  • Active comparator
    Tobacco Heating System

    Smokers who self-selected to switch to THS use.

    Other: THS

  • Active comparator
    Smoking Abstinence

    Smokers who self-selected to abstain from smoking.

    Other: Smoking Abstinence

Interventions

  • OtherCigarette

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

  • OtherTHS

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

    Also known as: Tobacco Heating System 3.0

  • OtherSmoking 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.)

06

What researchers measure

Primary outcomes

  1. Flow mediated dilation

    Change from baseline in flow mediated dilation (%FMD) of the brachial artery at 12 months before administration of a vasodilator (nitroglycerin)

    Time frame: From baseline to 12 months.

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 18, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05566678
Lead sponsor
Philip Morris Products S.A.
Responsible party
Sponsor
First posted
Oct 4, 2022
Start date
Mar 15, 2023
Primary completion
Mar 31, 2023
Completion
Mar 31, 2023
Last update
Nov 18, 2024

Study contacts

Christelle Haziza, PhD
study chair · Philip Morris Products S.A.

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Nov 2024. You cannot join it, but the record below documents what was studied.

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