Investigating the Lowest Threshold of Vascular Benefits From LDL Cholesterol Lowering in Patients With Stable CV Disease (INTENSITY-HIGH)

INvestigating the Lowest Threshold of Vascular bENefits From LDL Cholesterol Lowering With a PCSK9 mAb InhibiTor (Alirocumab) in Patients With Stable Cardiovascular Disease (INTENSITY-HIGH)

The INTENSITY-HIGH study aims to answer if there are any limits to LDL reduction in relation to benefiting vascular health, exploring the mechanisms by which secondary prevention in patients with established heart disease may benefit from even lower LDL levels. By using PCSK9 inhibitors such as Alirocumab, very low LDL cholesterol levels not previously encountered in statin trials, can be achieved in patients with established heart disease on top of intensive statin treatment.

This research is being carried out because it is unclear what the lowest threshold of LDL cholesterol should be to attain significant reductions in CV risk in stable cardiovascular patients. It is unknown whether there is a true limit of LDL cholesterol below which there is no further improvement in endothelial function in stable cardiovascular patients, and, whether this is associated with a reduction in markers of both systemic and vascular inflammation.

Defining this may help identify individuals from the general population who may benefit from more aggressive lipid lowering treatment than standard statin treatment in terms of CV morbidity and mortality.

This study will be conducted in patients with stable cardiovascular disease, where they will be randomized to receive either a combination of Alirocumab and statin, or Ezetimibe plus statin. 60 patients will be recruited to this single center, randomized, open label, parallel group, mechanistic physiological study which will be conducted at Cambridge University Hospitals NHS Foundation Trust. In order to be eligible for enrollment to the study, some patients may have to complete a 4 week washout period on a suitable statin therapy. The total study duration for each participant will be approximately 14 weeks, where a series of non-invasive vascular studies and medical imaging assessments which will be conducted to observe vascular/systemic inflammation and to assess endothelial vascular function.This study is funded by JP Moulton Charitable Foundation.

Study Overview

• Status: Active, not recruiting
• Conditions: Cardiovascular Diseases; Atherosclerosis
• Intervention / Treatment: Drug: Alirocumab 150 MG/ML; Drug: Atorvastatin 40Mg Tablet; Drug: Atorvastatin 80Mg Tablet; Drug: Rosuvastatin 20Mg Tablet; Drug: Rosuvastatin 40Mg Tablet; Drug: Simvastatin 80mg; Drug: Ezetimibe 10Mg Tablet

Detailed Description

The INTENSITY-HIGH study primarily seeks to explore the physiological mechanisms (mainly using endothelial function and vascular imaging of inflammation) by which secondary prevention in patients with established cardiovascular disease may benefit from even lower LDL levels using PCSK9 therapies. This will then set the basis for potential changes to guidelines about what a "healthy cholesterol" level should be and the targets these should be achieving, or indeed if there is a plateau beyond which there is no further benefit on surrogates of CV disease.

Endothelial function can be measured in the peripheral vasculature in a number of different ways, which include venous occlusion plethysmography with intra-arterial infusions of acetylcholine, ischemia flow-mediated endothelium-dependent dilatation (FMD) of the brachial artery, reactive hyperemia peripheral arterial tonometry (RH-PAT) and others. A venous plethysmography measure of forearm blood flow to intra-arterial acetylcholine infusion is the most sensitive and direct measurement of endothelium release of nitric oxides, but is more invasive than other techniques. FMD is non-invasive and measures changes in the brachial artery to ischemia. It is acknowledged that whilst FMD has a larger coefficient variation and is more technician dependent, it is more patient-friendly in that it is of shorter duration procedure wise, is non-invasive and is repeatable over a short period; therefore we have employed this technique in this study to improve chances of patient acceptability. RH-PAT is an alternative non-invasive assessment which measures volume changes at the fingertip (a surrogate of reactive hyperemia), is easy to implement and is not operator dependent. However, as yet it remains not well validated. Therefore, flow mediated dilatation has been selected for this study.

Metabolically active inflammatory cells utilize more glucose than non-activated cells, and the degree of metabolic activity can be measured using 18-fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT). Cellular FDG uptake is largely irreversible and correlates with glucose usage and macrophage numbers in both tumor cells and atherosclerotic plaques [38, 39]. FDG PET imaging has been successfully used to determine culprit plaques responsible for TIA and stroke [4042]. The signal has also been shown to be responsive to therapy, with clear reductions in FDG uptake noted in both humans and animal models of atherosclerosis [43, 44]. In addition, very recently, it has been shown that FDG-PET/CT is a reliable technique to assess changes in plaque structure with good reproducibility [40]. Taken together, these findings suggest a role for FDG PET/CT imaging in the assessment of the antiinflammatory potential of novel compounds such as PCSK9 therapies.

• Study Type: Interventional
• Enrollment (Actual): 60
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United Kingdom
  • Cambridgeshire
    • Cambridge, Cambridgeshire, United Kingdom, CB2 0QQ
      • Addenbrooke's Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 40 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Patients with high risk CVD with LDL-Cholesterol ≤ 4.0mmol* OR patients with very high risk CVD with LDL-Cholesterol ≤3.5mmol/l**
• Male or female patients over 40 years of age inclusive at screening, with a body weight ≥ 45kg and BMI ≥ 18 - ≤ 40kg/m2
• Palpable brachial arterial pulse, as per study team assessment
• History of stable CV disease, defined as previous myocardial infarction (STEMI or NSTEMI), angioplasty, documented CAD (Stress echo, CT coronary angiography or invasive angiography), stroke, TIA or peripheral vascular disease without a recent event in the last 6 months (i.e. acute coronary syndrome, unstable angina, CABG, PCI, stroke, MI, carotid endarterectomy)
• Stable 'suitable statin therapy' over the last 6 weeks as defined by a "statin equivalent" of Simvastatin 80mg od, Rosuvastatin 20mg/40mg od or Atorvastatin 40/80mg od. If not on stable statin therapy, a willingness to commence statin therapy or, if already on statin therapy, a willingness to increase statin therapy to fit the "statin equivalent" dose required in the study (as open label therapy) during run-in period
• Patients not taking Ezetimibe, or, if on Ezetimibe willingness to be washed out prior to randomisation

High risk is defined as a history of any of the following: acute coronary syndrome (such as myocardial infarction or unstable angina requiring hospitalisation), coronary or other arterial revascularisation procedures, chronic heart disease, ischaemic stroke, peripheral arterial disease.

Very high risk is defined as recurrent cardiovascular events or cardiovascular events in more than 1 vascular bed (that is, polyvascular disease).

Exclusion Criteria:

• Uncontrolled hypertension BP > 180/110 mmHg on repeated measurements
• Fasting hypertriglyceridemia with fasting TG>10 mmol/L at screening
• Pregnancy or combined oral contraceptive pill or hormone replacement therapy or childbearing potential
• Any concomitant condition that, at the discretion of the investigator, may affect the participant's ability to complete the study
• Any known sensitivity to Alirocumab or monoclonal antibodies
• Patients with history of hypersensitivity reactions to any of the study drugs
• History of significant LFT's (3xULN ALT or AST elevation) by previous statin treatment
• History of previous myositis associated with statin treatment (i.e. myalgias or asymptomatic CK elevation > 5 x ULN)
• Type 1 or Type 2 diabetes, which is insulin dependent or on oral hypoglycaemics/diet with HbA1c (DCCT) > 8% (OR HbA1c (IFCC) > 64mmol/mol) at screening. Please note: fasting glucose to be checked again at first FDG-PET/CT scan, and if glucose > 11mol/L at that visit, patients will be excluded from the study
• History of any acute CV event within 6 months prior to the screening period
• Rheumatoid arthritis, connective tissue disorders and other conditions known to be associated with active chronic inflammation (e.g. Inflammatory Bowel Disease)
• Untreated hypothyroidism, known autoimmune myositis
• Patients with CKD (defined as eGFR < 30 ml/min/1.73m2) at baseline will be excluded from the study
• Participant in a previous research study in the last 3 years which involved exposure to significant ionising radiation (i.e. cumulative research radiation dose > 5 mSv)
• History of malignancy within the past 5 years (with the exception of localised carcinoma of the skin that has been resected for cure)
• History of alcohol/drug abuse or dependence within 6 months of the study, screening visit 1
• Use of systemic corticosteroids at the time of scanning or a period of 2 weeks prior to screening visit
• Lack of ability to provide informed consent
• An unwillingness for female patients of childbearing potential to use an effective form of contraception (see section 12.2.3)
• Treatment with medications that result in significant drug to drug interactions with study medications. Assignment to a specific statin will be allowed prior to randomisation on a case-to-case basis dependent on the interactions with concomitant medications

Inclusion/Exclusion Criteria for INTENSITY-HIGH PET/MR sub-study (optional)

• Patient meets Inclusion/Exclusion criteria for INTENSITY HIGH
• Patient who fulfills the local imaging centre requirements for being scanned in the PET/MR machine will be enrolled
• Patient is willing to consent to participate in the sub-study

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Basic Science
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Alirocumab Treatment Arm; 30 patients with stable cardiovascular disease to receive Alirocumab 150mg & prescribed one of the following: Atorvastatin 40mg/80mg or Simvastatin 80mg or Rosuvastatin 20mg/40mg. Dosing and dispensing to be performed at V3, V4, V5 and V6.	Drug: Alirocumab 150 MG/ML; Dosing to be performed by subcutaneous injection in clinic; Other Names: Praluent; Drug: Atorvastatin 40Mg Tablet; Patients will be instructed to take once daily at night. Atorvastatin will be the preferred statin option for those with eGFR < 60 ml/min/1.73m2. Patient may be required to complete a 4 week run-in period on a statin prior to entering the study (dependent on eligibility); Drug: Atorvastatin 80Mg Tablet; Patients will be instructed to take once daily at night. Atorvastatin will be the preferred statin option for those with eGFR < 60 ml/min/1.73m2. Patient may be required to complete a 4 week run-in period on a statin prior to entering the study (dependent on eligibility); Drug: Rosuvastatin 20Mg Tablet; Patients will be instructed to take once daily at night. Rosuvastatin only to be prescribed if atorvastatin and simvastatin are not previously tolerated. Patient may be required to complete a 4 week run-in period on a statin prior to entering the study (dependent on eligibility); Other Names: Crestor; Drug: Rosuvastatin 40Mg Tablet; Patients will be instructed to take once daily at night. Rosuvastatin only to be prescribed if atorvastatin and simvastatin are not previously tolerated. Patient may be required to complete a 4 week run-in period on a statin prior to entering the study (dependent on eligibility); Other Names: Crestor; Drug: Simvastatin 80mg; Patients will be instructed to take once daily at night. Patient may be required to complete a 4 week run-in period on a statin prior to entering the study (dependent on eligibility)
Active Comparator: Comparator Treatment Arm; 30 patients with stable cardiovascular disease to receive Ezetimibe 10mg & prescribed one of the following: Atorvastatin 40mg/80mg or Simvastatin 80mg or Rosuvastatin 20mg/40mg. Dosing and dispensing to be performed at V3, V4, V5 and V6.	Drug: Atorvastatin 40Mg Tablet; Patients will be instructed to take once daily at night. Atorvastatin will be the preferred statin option for those with eGFR < 60 ml/min/1.73m2. Patient may be required to complete a 4 week run-in period on a statin prior to entering the study (dependent on eligibility); Drug: Atorvastatin 80Mg Tablet; Patients will be instructed to take once daily at night. Atorvastatin will be the preferred statin option for those with eGFR < 60 ml/min/1.73m2. Patient may be required to complete a 4 week run-in period on a statin prior to entering the study (dependent on eligibility); Drug: Rosuvastatin 20Mg Tablet; Patients will be instructed to take once daily at night. Rosuvastatin only to be prescribed if atorvastatin and simvastatin are not previously tolerated. Patient may be required to complete a 4 week run-in period on a statin prior to entering the study (dependent on eligibility); Other Names: Crestor; Drug: Rosuvastatin 40Mg Tablet; Patients will be instructed to take once daily at night. Rosuvastatin only to be prescribed if atorvastatin and simvastatin are not previously tolerated. Patient may be required to complete a 4 week run-in period on a statin prior to entering the study (dependent on eligibility); Other Names: Crestor; Drug: Simvastatin 80mg; Patients will be instructed to take once daily at night. Patient may be required to complete a 4 week run-in period on a statin prior to entering the study (dependent on eligibility); Drug: Ezetimibe 10Mg Tablet; Patients will be instructed to take once daily at night.; Other Names: Ezetrol

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Vascular inflammation (Standard Uptake Value) - Carotid artery	Change in vascular inflammation in the carotid artery between Alirocumab and Ezetimibe treatment regimes (Vascular inflammation will be quantified by calculating the Standard Uptake Value [SUV])	8 weeks
Vascular inflammation (Tissue to Background Ratio TBR) - Carotid artery	Change in vascular inflammation in the carotid artery between Alirocumab and Ezetimibe treatment regimes (Vascular inflammation will be quantified by calculating the Tissue to Background Ratio [TBR])	8 weeks
Vascular inflammation (Standard Uptake Value) - Aortic artery	Change in vascular inflammation in the aortic artery between Alirocumab and Ezetimibe treatment regimes (Vascular inflammation will be quantified by calculating the Standard Uptake Value [SUV])	8 weeks
Vascular inflammation (Tissue to Background Ratio TBR) - Aortic artery	Change in vascular inflammation in the aortic artery between Alirocumab and Ezetimibe treatment regimes (Vascular inflammation will be quantified by calculating the Tissue to Background Ratio [TBR])	8 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Endothelial-dependent vasodilatation (as measured by Flow Mediated Dilatation using high-resolution vascular ultrasound)	Comparing the effects of Alirocumab or Ezetimibe treatment regimes on Flow Mediated Dilatation (a surrogate of endothelial-dependent vasodilatation)	8 weeks
Endothelial-independent vasodilatation (as measured by Flow Mediated Dilatation using high-resolution vascular ultrasound)	Comparing the effects of Alirocumab or Ezetimibe treatment regimes on sublingual glyceryl trinitrate (GTN) response to Flow Mediated Dilatation (a surrogate of endothelial-independent vasodilatation)	8 weeks
Augmentation index (an indicator of arterial stiffness)	Change in Augmentation Index between visits and between Alirocumab or Ezetimibe treatment regimes	8 weeks
Pulse wave velocity	Change in aortic Pulse Wave Velocity between visits and between Alirocumab or Ezetimibe treatment regimes	8 weeks
Carotid IMT	Change in Carotid IMT between visits and between Alirocumab or Ezetimibe treatment regimes	8 weeks
Systemic inflammation (as measured by lipid profile)	Change in systemic inflammation (as measured by lipid profile) between visits and between Alirocumab or Ezetimibe treatment regimes	8 weeks
Systemic inflammation (as measured by hsCRP)	Change in systemic inflammation (as measured by hsCRP) between visits and between Alirocumab or Ezetimibe treatment regimes	8 weeks
Systemic inflammation (as measured by MMP9)	Change in systemic inflammation (as measured by MMP9) between visits and between Alirocumab or Ezetimibe treatment regimes	8 weeks
Systemic inflammation (as measured by IL2)	Change in systemic inflammation (as measured by IL2) between visits and between Alirocumab or Ezetimibe treatment regimes	8 weeks
Systemic inflammation (as measured by IL6)	Change in systemic inflammation (as measured by IL6) between visits and between Alirocumab or Ezetimibe treatment regimes	8 weeks
Systemic inflammation (as measured by oxLDL lipid subfractions)	Change in systemic inflammation (as measured by oxLDL lipid subfractions) between visits and between Alirocumab or Ezetimibe treatment regimes	8 weeks

Collaborators and Investigators

• Sponsor: Cambridge University Hospitals NHS Foundation Trust
• Collaborators: University of Cambridge
• Investigators: Principal Investigator: Joseph Cheriyan, MBChB, FRCP, MA, Cambridge University Hospitals NHS Trust; Principal Investigator: Michalis Kostapanos, MD, PhD, FRSPH, Cambridge University Hospitals NHS Trust

Publications and helpful links

General Publications

• Cacciottolo PJ, Kostapanos MS, Hernan Sancho E, Pavey H, Kaloyirou F, Vamvaka E, Helmy J, Hubsch A, McEniery CM, Wilkinson IB, Cheriyan J. Investigating the Lowest Threshold of Vascular Benefits from LDL Cholesterol Lowering with a PCSK9 mAb Inhibitor (Alirocumab) in Patients with Stable Cardiovascular Disease (INTENSITY-HIGH): protocol and study rationale for a randomised, open label, parallel group, mechanistic study. BMJ Open. 2021 Apr 13;11(4):e037457. doi: 10.1136/bmjopen-2020-037457.

Study record dates

Study Major Dates

• Study Start (Actual): November 30, 2017
• Primary Completion (Actual): September 30, 2019
• Study Completion (Anticipated): November 30, 2023

Study Registration Dates

• First Submitted: October 6, 2017
• First Submitted That Met QC Criteria: November 21, 2017
• First Posted (Actual): November 28, 2017

Study Record Updates

• Last Update Posted (Actual): July 23, 2021
• Last Update Submitted That Met QC Criteria: July 22, 2021
• Last Verified: July 1, 2021

More Information

Terms related to this study

• Keywords: Inflammation; Endothelial function; Arterial Stiffness; PCSK9; Ezetimibe; Low Density Lipoprotein Cholesterol (LDL); Alirocumab; Flow Mediated Dilatation; Carotid Intima Media Thickness; FDG PET-CT; PET-MR
• Additional Relevant MeSH Terms: Vascular Diseases; Arteriosclerosis; Arterial Occlusive Diseases; Cardiovascular Diseases; Atherosclerosis; Molecular Mechanisms of Pharmacological Action; Enzyme Inhibitors; Antimetabolites; Anticholesteremic Agents; Hypolipidemic Agents; Lipid Regulating Agents; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Atorvastatin; Rosuvastatin Calcium; Simvastatin; Ezetimibe
• Other Study ID Numbers: INTENSITY-HIGH

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No
• IPD Plan Description: Only the minimum required participant identifiable information (name and contact details) will be provided to the research team for the purpose of arranging study visits and completing the informed consent process. All delegated research personnel that is responsible to conduct the data/statistical analysis will only analyse data that is anonymised of any patient identifiable data.

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No