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NCT Number: NCT04073797

PET Imaging of Inflammation and Lipid Lowering Study

While 18F-fluorodeoxyglucose (FDG) positron emission tomography (PET) imaging has been used as an early marker of drug efficacy in numerous clinical cardiovascular drug trials, as a glucose analog, its signal in the vasculature lacks inflammatory cell-specificity. Moreover, high background 18F-FDG signals from the myocardium often preclude coronary artery imaging, despite attempts to suppress myocardial tracer uptake by dietary manipulation. These limitations of 18F-FDG for measuring changes in vascular inflammation arising from drug intervention highlight important unmet needs, which might be overcome by using a somatostatin receptor subtype-2 (SST2) PET tracer.

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Key information

About this study

Up-regulation of SST2 in activated macrophages represents a novel imaging target for measuring vascular inflammation, which has been previously examined in atherosclerosis using 68Ga-DOTATATE. To test the hypothesis that 68Ga-DOTATATE can quantify drug-induced changes in arterial inflammation, patients with primary hypercholesterolaemia (non-familial or familial) or mixed dyslipidaemia with stable cardiovascular Disease (CVD) and elevated LDL cholesterol ≥2.6 despite maximum tolerated statins with or without other lipid lowering therapies will undergo carotid artery 68Ga-DOTATATE PET-magnetic resonance imaging (MRI) in a randomised, double-blind, placebo-controlled study of inclisiran or colchicine.

In parallel, we will examine a novel method for detecting plaque composition based on analysis of ultrasound centre frequency shifts, which was developed by collaborators in Lund University, Sweden. The Ultrasound Plaque Structure Analysis (UPSA) method uses radiofrequency algorithms to create real-time tissue-like maps of carotid plaques. Participants in the study will undergo carotid ultrasound imaging using the UPSA method in addition to PET/MRI.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Male or female participants >18 years old
  • Able to give written, informed consent and to lie flat
  • Have primary hypercholesterolaemia (non-familial or definite or possible heterozygous familial hypercholesterolaemia (HeFH) based on clinical criteria) or mixed dyslipidaemia, and
  • History of CVD (acute coronary syndrome, coronary or other revascularisation procedures, coronary heart disease, ischaemic stroke, or peripheral arterial disease) and elevated LDL cholesterol ≥2.6 despite maximum tolerated statins with or without other lipid lowering therapies (see NICE TA 733), and
  • Lipid lowering therapy unchanged for at least 6 weeks prior to screening, and
  • Pre-existing carotid atherosclerotic plaque ≥15mm by B-mode ultrasound

Exclusion criteria

  • Women of childbearing potential not using adequate contraception
  • Contra-indication to MRI scanning
  • Statin-associated myositis or liver function abnormality
  • Already taking inclisiran or colchicine
  • Sensitivity and/or contraindication to inclisiran or colchicine. Contraindications to colchicine include severe hepatic or renal impairment, blood disorders, and patients with renal or hepatic impairment who are taking a P-gp inhibitor or a strong CYP3A4 inhibitor
  • Contrast allergy or contrast-nephropathy
  • Chronic kidney disease (eGFR <30 mL/min/1.73 m2)
  • Cardiovascular event within 6 months
  • Any medical condition, in the opinion of the investigator, that prevents the participant from lying flat during scanning, or from participating in the study
  • Uncontrolled chronic inflammatory disorder
  • History of recent malignancy deemed relevant to the study by the investigator
  • Treatment with medications that result in significant drug to drug interactions with the study medications
  • Current use of systemic corticosteroids or other immunosuppressive drugs
  • Previous or planned carotid endarterectomy surgery or stenting on the index side

Treatment and study plan

Inclisiran

Drug

Inclisiran 284 mg, one injection

68Ga-DOTATATE PET-MRI

Diagnostic Test

68Ga-DOTATATE PET-MRI at baseline and 12 weeks

Colchicine

Drug

Colchicine 500 mcg tablet once daily

Primary outcomes

  1. Carotid 68Ga-DOTATATE PET

    Time frame: 12 weeks

    Relative change from baseline in carotid artery 68Ga-DOTATATE tissue-to-blood ratio in the index vessel

  2. Carotid UPSA imaging

    Time frame: 12 weeks

    Relative change from baseline in carotid artery UPSA signal in the index vessel

Secondary outcomes

  1. MRI plaque burden

    Time frame: 12 weeks

    Relative change from baseline in carotid artery total plaque burden and lipid-rich necrotic core measured by MRI

  2. Carotid 68Ga-DOTATATE vs. serum lipids

    Time frame: 12 weeks

    Comparison of carotid 68Ga-DOTATATE imaging to serum lipids

  3. Carotid 68Ga-DOTATATE vs. hsCRP

    Time frame: 12 weeks

    Comparison of carotid 68Ga-DOTATATE imaging to high-sensitivity C-reactive protein (hsCRP)

Study contacts

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

Jason M Tarkin, MBBS PhD

CONTACT

[email protected]

+44(0)1223331504

Sponsors and collaborators

Lead sponsor

University of Cambridge

Other

Collaborators

  • Cambridge University Hospitals NHS Foundation Trust
  • GE Healthcare
  • Lund University
  • Wellcome Trust

Registry information

Acronym: PIILL

Important dates

Study start
2023
Primary completion
2025
Study completion
2026
First posted
Aug 29, 2019
Registry last updated
Jul 19, 2024

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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