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NCT Number: NCT06863545

Further Lipid-Lowering With PCSK9 Inhibitors for Cardiovascular Outcomes in High-Risk Coronary Plaques Assessed by CT Angiography

The primary objective was to evaluate the effect of PCSK9 inhibitors in addition to the background lipid-modifying therapy (LMT), compared with standard LMT in terms of clinical outcomes in patients with coronary CT angiography (CCTA)-detected high-risk plaques.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Zhejiang Provincial Hospital of Traditional Chinese Medicine, Hangzhou, Zhejiang, China

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About this study

CCTA is an accurate, noninvasive alternative to invasive coronary angiography. CCTA can provide detailed information about the characteristics of coronary artery plaques, such as their composition, morphology, and distribution. Various CCTA-detected plaque characteristics indicative of plaque quantity and quality have been identified as high-risk features independently predicting clinical events, including the presence of positive remodeling, low attenuation plaque, spotty calcification, and napkin ring sign. Currently, the treatment for CCTA-detected high-risk plaque has been receiving increasing interest. The current study aimed to prove the efficacy of PCSK9 inhibitors in addition to the background LMT, as compared with standard LMT in patients with CCTA-detected high-risk plaques.

Hypothesis: PCSK9 inhibitors in addition to background LMT will show a superior event rate, compared with standard LMT, in terms of major adverse cardiac and cerebrovascular events (MACCEs) at 24 months after the last patient's randomization in patients with high-risk coronary plaques assessed by CT Angiography.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject must be ≥ 18 years.
  • Patients with at least one target lesion meet CCTA-detected plaque features of the following:
  • Degree of stenosis ≥ 50% or plaque burden ≥ 70%
  • At least 2 of the following high-risk plaque features:

i. Low-attenuation plaque ii. Positive remodeling iii. Napkin-ring sign iv. Spotty calcium

  • The target lesion is located at the proximal or mid segment of left anterior descending artery, left circumflex artery or right coronary artery.
  • Subject is able to confirm his/her understanding of the risks, benefits, and treatment alternatives of receiving study-related treatment. He/she or his/her legally authorized representative provides written informed consent prior to any study-related procedure.

Exclusion criteria

  • Target lesions underwent or planned to revascularization.
  • Patients with acute coronary syndrome.
  • New York Heart Association class III or IV, or last known left ventricular ejection fraction < 30%.
  • Uncontrolled or recurrent ventricular tachycardia.
  • Homozygous familial hypercholesterolemia.
  • Active liver disease or hepatic dysfunction.
  • Failed CCTA plaque analysis.
  • Non-cardiac co-morbid conditions with life expectancy < 2 years.
  • Pregnant and/or lactating women.
  • Known hypersensitivity or contraindication to statin or PCSK9 inhibitors.

Treatment and study plan

PCSK9 inhibitors and background lipid-modifying therapy

Drug

Patients will receive subcutaneous injections of PCSK9 inhibitors and oral administration of background LMT (including statins and/or cholesterol absorption inhibitors) for the first 12 months after randomization, with PCSK9 inhibitors administered every 2 weeks. After the first 12 months, patients will discontinue the PCSK9 inhibitors but continue background LMT for the remainder of the trial.

Standard lipid-modifying therapy

Drug

Patients will receive standard LMT commonly used in clinical practice.

Primary outcomes

  1. Major adverse cardiac and cerebrovascular events (MACCEs)

    Time frame: 24 months after the last patient's randomization

    A composite of death from any cause, myocardial infarction (MI), coronary revascularization, or stroke.

Secondary outcomes

  1. MACCEs

    Time frame: 60 months after the last patient's randomization

    a composite of death from any cause, MI, coronary revascularization, or stroke.

  2. Individual component of MACCEs.

    Time frame: 24 and 60 months after the last patient's randomization

    Individual component of MACCEs (death from any cause, MI, coronary revascularization, or stroke)

  3. Major adverse cardiovascular events (MACEs)

    Time frame: 24 and 60 months after the last patient's randomization

    Defined as a composite of death from any cause, MI, coronary revascularization.

  4. Target vessel failure (TVF)

    Time frame: 24 and 60 months after the last patient's randomization

    Defined as a composite of cardiac death, target-vessel MI, or target vessel revascularization

  5. Cost-effectiveness analysis

    Time frame: 24 and 60 months after the last patient's randomization

    Cost-effectiveness analysis

  6. All-cause and cardiac death.

    Time frame: 24 and 60 months after the last patient's randomization

    All-cause and cardiac death.

  7. Any target-vessel MI.

    Time frame: 24 and 60 months after the last patient's randomization

    Any target-vessel MI.

  8. Any target vessel revascularization.

    Time frame: 24 and 60 months after the last patient's randomization

    Any target vessel revascularization.

  9. Any coronary revascularization (ischemia-driven or all).

    Time frame: 24 and 60 months after the last patient's randomization

    Any coronary revascularization (ischemia-driven or all).

  10. CT coronary angiography findings

    Time frame: 36 months after the last patient's randomization

    Changes in the CT-derived fractional flow reserve, lumen, plaque quantity and quality between baseline.

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Second Affiliated Hospital, School of Medicine, Zhejiang University

Other

Registry information

Acronym: FLAVOUR IV

Important dates

Study start
2025
Primary completion
2030
Study completion
2033
First posted
Mar 7, 2025
Registry last updated
Feb 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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