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临床试验/NCT05566678
NCT05566678撤回不适用

A 12-month, 3-group, Preference, Multi-center Study to Demonstrate the Effects of Switching From Cigarettes to Tobacco Heating System (THS) on Systemic Endothelial Function in Subjects With Established Atherosclerotic Disease

Philip Morris Products S.A.0 个研究点开始时间: 2023年3月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
主要终点
Flow mediated dilation

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
40 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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 V
  • •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 V
  • •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

排除标准

  • •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 V
  • •Recent ACS / myocardial infarction or stroke / TIA <30 days prior to V
  • •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 V
  • •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]

研究组 & 干预措施

Cigarette

Active Comparator

Smokers who self-selected to continue smoking cigarettes.

干预措施: Cigarette (Other)

Tobacco Heating System

Active Comparator

Smokers who self-selected to switch to THS use.

干预措施: THS (Other)

Smoking Abstinence

Active Comparator

Smokers who self-selected to abstain from smoking.

干预措施: Smoking Abstinence (Other)

结局指标

主要结局

Flow mediated dilation

时间窗: From baseline to 12 months.

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

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

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