Skip to main content
TrialFinder
TrialFinder is for informational purposes only and does not provide medical advice. Always talk to your doctor about whether a trial is right for you.
RECRUITINGINTERVENTIONAL

PET Imaging of Inflammation and Lipid Lowering Study

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: - Male or female participants \>18 years old - Able to give written, willing to sign a consent form 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 Who Should NOT Join This Trial: - 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 Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
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

Treatments Being Tested

DRUG

Inclisiran

Inclisiran 284 mg, one injection

DIAGNOSTIC_TEST

68Ga-DOTATATE PET-MRI

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

DRUG

Colchicine

Colchicine 500 mcg tablet once daily

Locations (1)

University of Cambridge
Cambridge, United Kingdom