Impact of PCSK9 Inhibitors on Coronary Microvascular Dysfunction in Patients With Atherosclerotic Cardiovascular Disease Proved by Myocardial Ischemia and Needing Coronarography (MICROPROTECT)
Primary Purpose
Atherosclerotic Cardiovascular Disease
Status
Recruiting
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Evolocumab 140 MG/ML [Repatha]
Sponsored by
About this trial
This is an interventional treatment trial for Atherosclerotic Cardiovascular Disease focused on measuring Proprotein convertase subtilisin/kexin type 9 inhibitor monoclonal antibody (Anti-PCSK9), Microvascular coronary dysfunction (CMVD), Coronary angioplasty, Cardiovascular imaging
Eligibility Criteria
Inclusion Criteria:
- Male or female patient, aged 40 to 85,
- More than 50 kilograms
- Defined at high cardiovascular risk according to European guidelines
- LDL-C level ≥ 0.7 g / L (biological assessment of less than 6 months)
- Having benefited from myocardial scintigraphy
- For which coronarography is indicated according to European guidelines
- Affiliated with social security,
- Signed informed consent form
Exclusion Criteria:
- Clinical presentation of unstable angina
- Patient whose state of physical or psychological health could compromise the obtaining of his informed consent and his compliance with the requirements of the protocol, with the study evaluation, procedures or completion.
- End stage disease (estimated survival of less than one year)
- Severe renal dysfunction, defined as an estimated creatinine clearance (MDRD) < 30 mL/min at screening
- Contra-indication to adenosin : hypersensitivity to active active substance or to any of the excipients, type II or III atrioventricular block or atrial disease (except for pacemaker users), long QT syndrome, severe arterial hypotension, acute heart failure, asthma and severe chronic obstructive pulmonary disease, unstable angina unstabilized by drug therapy, taking dipyridamole, aminophylline, theophylline or other xanthine base within 24 hours prior to adenosine administration
- Contra-indication to heparin: hypersensitivity to active substance or to any of the excipients, past heparin induced thrombopenia type II, haemorrhage.
- Prior Coronary Artery Bypass Graft Surgery (CABG)
- Prior myocardial infarction in the territory of ischemia
- New York Heart Association (NYHA) class III or IV, or last known left ventricular ejection fraction < 30%
- Known hemorrhagic stroke at any time
- Uncontrolled or recurrent ventricular tachycardia
- Uncontrolled hypertension defined as sitting systolic blood pressure (SBP) > 180 mmHg or diastolic BP (DBP) > 110 mmHg
- Actual use of PCSK9 inhibitor (evolocumab or others)
- Untreated or inadequately treated hyperthyroidism or hypothyroidism, controlled by biological assessment if needed, defined by thyroid stimulating hormone (TSH) < lower limit of normal (LLN) or > 1.5 times the upper limit of normal (ULN), respectively, and free thyroxine (T4) levels that are outside normal range at screening
- Active liver disease or hepatic dysfunction, defined as aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 3 times the ULN at screening
- Recipient of any major organ transplant (eg, lung, liver, heart, bone marrow, renal)
- Personal or family history of hereditary muscular disorders
- LDL apheresis within 12 months prior to randomization
- Creatinine Phosphokinase (CPK) > 5 ULN at screening
- Active infection or others active disease judge by investigator incompatible with the protocol completion
- Main known active infection including positive viral serology (Human Immunodeficiency Virus, Hepatitis B Virus and Hepatitis C Virus)
- Malignancy (except non-melanoma skin cancers, cervical in-situ carcinoma, breast ductal carcinoma in situ, or stage 1 prostate carcinoma) within the last 10 years
- Known sensitivity to evolocumab or their excipients to be administered during dosing or natural rubber / latex
- Patient likely to not be available to complete all protocol-required study visits or procedures.
- Patient in exclusion period of another study
- Woman able to procreate in the absence of highly effective contraception
- Persons referred to in Articles L1121-6 to L1121-8 of the French code of public health (this corresponds to all persons protected: pregnant or parturient women, breastfeeding mothers, persons deprived of liberty by judicial or administrative decision, persons subject to a legal protection measure).
Sites / Locations
- Grenoble University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Evolocumab, 420 milligrams
Control arm
Arm Description
Single injection of 420 milligrams of evolocumab (REPATHA®) one month before coronary angiography and coronary microcirculation (IMR) measurement.
Measurement of coronary microcirculation (IMR) during coronary angiography, without prior evolocumab injection.
Outcomes
Primary Outcome Measures
Impact of a PCSK9 inhibitor treatment on coronary microvascular dysfunction (CMVD) at 4 weeks in patients with atherosclerotic cardiovascular disease.
Index of microcirculatory resistance (IMR), measured during invasive coronary angiography and expressed in mmHg.s
Secondary Outcome Measures
Impact of a PCSK9 inhibitor treatment on soluble VE-cadherin rate (sVE).
Measurement of sVE rate at baseline and four weeks after treatment with evolocumab or without treatment.
Impact of a PCSK9 inhibitor treatment on brachial hyperemia (HB).
Variation of the luminal diameter of the humeral artery with baseline and four weeks after treatment with evolocumab or without treatment.
Impact of a PCSK9 inhibitor treatment on the rate of peri-procedural myocardial infarction.
Troponin I level after PCI (peri-procedural myocardial pain will be defined as a post-angioplasty troponin level 10 times higher than the 99th percentile of troponin I).
Correlations between invasive and non-invasive (myocardial scintigraphy - myocardial perfusion entropy (MPE), concentration of sVE, HB) measurements of coronary microvascular dysfunction.
IMR, MPE, sVE and the variation of the luminal diameter of the humeral artery.
Correlations between the cardiovascular risk and the concentration of sVE and MPE.
Risk score, sVE rate and MPE.
Full Information
NCT ID
NCT04338165
First Posted
April 3, 2020
Last Updated
May 18, 2022
Sponsor
University Hospital, Grenoble
1. Study Identification
Unique Protocol Identification Number
NCT04338165
Brief Title
Impact of PCSK9 Inhibitors on Coronary Microvascular Dysfunction in Patients With Atherosclerotic Cardiovascular Disease Proved by Myocardial Ischemia and Needing Coronarography
Acronym
MICROPROTECT
Official Title
Effect of Impact of PCSK9 Inhibitors on Coronary Microvascular Dysfunction in Patients With Atherosclerotic Cardiovascular Disease Proved by Myocardial Ischemia and Needing Coronarography : a Monocentric, Prospective, Randomized and Open-label Phase II Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 8, 2021 (Actual)
Primary Completion Date
November 2022 (Anticipated)
Study Completion Date
November 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Grenoble
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Proprotein convertase subtilisin/kexin type 9 inhibitor monoclonal antibodies (anti-PCSK9) significantly reduce the serum LDL-C level, leading to a regression of the coronary epicardial plaque demonstrated by intracoronary ultrasonography (IVUS), as well as cardiovascular events (CV) in patients with atherosclerotic CV disease treated with statin. The impact of PCSK9 inhibition on coronary microcirculation has never been assessed. However, microvascular coronary dysfunction (CMVD) is a powerful prognostic marker, irrespective of conventional CV risk factors, but also of the severity of the epicardial coronary involvement detected during coronary angiography. The investigators hypothesized that anti-PCSK9 would decrease CMVD, measured by the microcirculatory resistance index (MRI) during coronary angioplasty (Percutaneous coronary intervention, PCI) in patients with myocardial ischemia proved in myocardial scintigraphy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atherosclerotic Cardiovascular Disease
Keywords
Proprotein convertase subtilisin/kexin type 9 inhibitor monoclonal antibody (Anti-PCSK9), Microvascular coronary dysfunction (CMVD), Coronary angioplasty, Cardiovascular imaging
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
66 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Evolocumab, 420 milligrams
Arm Type
Experimental
Arm Description
Single injection of 420 milligrams of evolocumab (REPATHA®) one month before coronary angiography and coronary microcirculation (IMR) measurement.
Arm Title
Control arm
Arm Type
No Intervention
Arm Description
Measurement of coronary microcirculation (IMR) during coronary angiography, without prior evolocumab injection.
Intervention Type
Drug
Intervention Name(s)
Evolocumab 140 MG/ML [Repatha]
Intervention Description
3 injections of evolocumab 140 milligrams performed within 30 minutes and self-administered (subcutaneously in the abdomen, thigh, or upper arm)
Primary Outcome Measure Information:
Title
Impact of a PCSK9 inhibitor treatment on coronary microvascular dysfunction (CMVD) at 4 weeks in patients with atherosclerotic cardiovascular disease.
Description
Index of microcirculatory resistance (IMR), measured during invasive coronary angiography and expressed in mmHg.s
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Impact of a PCSK9 inhibitor treatment on soluble VE-cadherin rate (sVE).
Description
Measurement of sVE rate at baseline and four weeks after treatment with evolocumab or without treatment.
Time Frame
4 weeks
Title
Impact of a PCSK9 inhibitor treatment on brachial hyperemia (HB).
Description
Variation of the luminal diameter of the humeral artery with baseline and four weeks after treatment with evolocumab or without treatment.
Time Frame
4 weeks
Title
Impact of a PCSK9 inhibitor treatment on the rate of peri-procedural myocardial infarction.
Description
Troponin I level after PCI (peri-procedural myocardial pain will be defined as a post-angioplasty troponin level 10 times higher than the 99th percentile of troponin I).
Time Frame
4 weeks
Title
Correlations between invasive and non-invasive (myocardial scintigraphy - myocardial perfusion entropy (MPE), concentration of sVE, HB) measurements of coronary microvascular dysfunction.
Description
IMR, MPE, sVE and the variation of the luminal diameter of the humeral artery.
Time Frame
4 weeks
Title
Correlations between the cardiovascular risk and the concentration of sVE and MPE.
Description
Risk score, sVE rate and MPE.
Time Frame
4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female patient, aged 40 to 85,
More than 50 kilograms
Defined at high cardiovascular risk according to European guidelines
LDL-C level ≥ 0.7 g / L (biological assessment of less than 6 months)
Having benefited from myocardial scintigraphy
For which coronarography is indicated according to European guidelines
Affiliated with social security,
Signed informed consent form
Exclusion Criteria:
Clinical presentation of unstable angina
Patient whose state of physical or psychological health could compromise the obtaining of his informed consent and his compliance with the requirements of the protocol, with the study evaluation, procedures or completion.
End stage disease (estimated survival of less than one year)
Severe renal dysfunction, defined as an estimated creatinine clearance (MDRD) < 30 mL/min at screening
Contra-indication to adenosin : hypersensitivity to active active substance or to any of the excipients, type II or III atrioventricular block or atrial disease (except for pacemaker users), long QT syndrome, severe arterial hypotension, acute heart failure, asthma and severe chronic obstructive pulmonary disease, unstable angina unstabilized by drug therapy, taking dipyridamole, aminophylline, theophylline or other xanthine base within 24 hours prior to adenosine administration
Contra-indication to heparin: hypersensitivity to active substance or to any of the excipients, past heparin induced thrombopenia type II, haemorrhage.
Prior Coronary Artery Bypass Graft Surgery (CABG)
Prior myocardial infarction in the territory of ischemia
New York Heart Association (NYHA) class III or IV, or last known left ventricular ejection fraction < 30%
Known hemorrhagic stroke at any time
Uncontrolled or recurrent ventricular tachycardia
Uncontrolled hypertension defined as sitting systolic blood pressure (SBP) > 180 mmHg or diastolic BP (DBP) > 110 mmHg
Actual use of PCSK9 inhibitor (evolocumab or others)
Untreated or inadequately treated hyperthyroidism or hypothyroidism, controlled by biological assessment if needed, defined by thyroid stimulating hormone (TSH) < lower limit of normal (LLN) or > 1.5 times the upper limit of normal (ULN), respectively, and free thyroxine (T4) levels that are outside normal range at screening
Active liver disease or hepatic dysfunction, defined as aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 3 times the ULN at screening
Recipient of any major organ transplant (eg, lung, liver, heart, bone marrow, renal)
Personal or family history of hereditary muscular disorders
LDL apheresis within 12 months prior to randomization
Creatinine Phosphokinase (CPK) > 5 ULN at screening
Active infection or others active disease judge by investigator incompatible with the protocol completion
Main known active infection including positive viral serology (Human Immunodeficiency Virus, Hepatitis B Virus and Hepatitis C Virus)
Malignancy (except non-melanoma skin cancers, cervical in-situ carcinoma, breast ductal carcinoma in situ, or stage 1 prostate carcinoma) within the last 10 years
Known sensitivity to evolocumab or their excipients to be administered during dosing or natural rubber / latex
Patient likely to not be available to complete all protocol-required study visits or procedures.
Patient in exclusion period of another study
Woman able to procreate in the absence of highly effective contraception
Persons referred to in Articles L1121-6 to L1121-8 of the French code of public health (this corresponds to all persons protected: pregnant or parturient women, breastfeeding mothers, persons deprived of liberty by judicial or administrative decision, persons subject to a legal protection measure).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gilles Barone-Rochette, MD, PhD
Phone
+33476765172
Email
gbarone@chu-grenoble.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Clémence Charlon
Email
ccharlon@chu-grenoble.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gilles Barone-Rochette, MD, PhD
Organizational Affiliation
CHU Grenoble Alpes
Official's Role
Principal Investigator
Facility Information:
Facility Name
Grenoble University Hospital
City
Grenoble
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gilles Barone Rochette
Phone
0033476765172
Email
gbarone@chu-grenoble.fr
12. IPD Sharing Statement
Plan to Share IPD
No
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Impact of PCSK9 Inhibitors on Coronary Microvascular Dysfunction in Patients With Atherosclerotic Cardiovascular Disease Proved by Myocardial Ischemia and Needing Coronarography
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