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A Trial of Alirocumab and Plaque Regression in Peripheral Arterial Disease

Primary Purpose

Peripheral Arterial Disease

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Alirocumab
Matching placebo
Sponsored by
University of Virginia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Arterial Disease focused on measuring MRI, PCSK9 inhibition, LDL cholesterol

Eligibility Criteria

35 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 35-85
  • Clinical diagnosis of peripheral arterial disease
  • Ankle brachial index of 0.4-0.9
  • Either on statin for at least 6 months or statin intolerant. The statin used should be a high potency statin (Crestor, Lipitor) or high dose of a lower potency statin (e.g. Zocor 40-80mg, Pravachol 40-80 mg)

Exclusion Criteria:

  • rest pain
  • critical limb ischemia
  • known or planned stent in the SFA
  • known occlusion of the SFA
  • planned revascularization within the next year
  • inability to lie flat
  • known contraindications to MRI including pacemaker, implantable cardioverter defibrillators, certain intracranial aneurysm clips, claustrophobia
  • pregnancy
  • known allergy to alirocumab

Sites / Locations

  • Northwestern University
  • University of Virginia Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Alirocumab

Placebo

Arm Description

Alirocumab 150mg SQ every 2 weeks

Matched placebo

Outcomes

Primary Outcome Measures

Change in superficial femoral plaque volume (summed from both legs)
Measured by black blood MRI, expressed in cm3

Secondary Outcome Measures

Change in calf muscle perfusion in the most symptomatic leg
Measured by arterial spin labeling MRI, expressed in ml/min/100g
Change in plaque characteristics
% lipid in one slice from each leg
Change in 6-minute walk test
expressed in feet
Change in LDL cholesterol
Change in high sensitivity c-reactive protein
Change in fibrinogen
Change in lipoprotein (a)

Full Information

First Posted
November 4, 2016
Last Updated
May 8, 2023
Sponsor
University of Virginia
Collaborators
Northwestern University
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1. Study Identification

Unique Protocol Identification Number
NCT02959047
Brief Title
A Trial of Alirocumab and Plaque Regression in Peripheral Arterial Disease
Official Title
A Double Blind, Randomized Trial of Alirocumab and Plaque Regression in Peripheral Arterial Disease
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
July 17, 2017 (Actual)
Primary Completion Date
May 8, 2023 (Actual)
Study Completion Date
May 8, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia
Collaborators
Northwestern University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Peripheral arterial disease (PAD) is characterized by lower limb arterial obstruction due to atherosclerosis. Magnetic resonance imaging (MRI) methods can accurately quantify atherosclerotic plaque in the superficial femoral artery (SFA) in patients with PAD. Such techniques have demonstrated plaque regression with statin therapy over 1 year. Alirocumab is a PCSK9 inhibitor that effectively reduces LDL cholesterol up to 70% in patients on statins or intolerant to statins. The investigators hypothesize that effective low density lipoprotein (LDL) lowering with Alirocumab 150m subcutaneously (SQ) every 2 weeks will regress atherosclerotic plaque in the SFA in patients with PAD over one year compared to placebo. 54 patients with mild-moderate PAD (ankle brachial index or ABI 0.4-0.9) will be randomized to alirocumab 150 mg SQ every 2 weeks or matching placebo at the University of Virginia (UVA) (n=34) and Northwestern (n=20). The primary endpoint is change in atherosclerotic plaque volume in the superficial femoral artery over the 1 year treatment period. Secondary endpoints include changes in peak calf muscle perfusion after thigh cuff occlusion/hyperemia, 6-minute walk distance, and blood biomarkers (LDL cholesterol, fibrinogen, high sensitivity c-reactive protein (hs-CRP), and lipoprotein(a).
Detailed Description
PAD is characterized by lower limb arterial obstruction due to atherosclerosis. There are over 8.5 million people with PAD in the U.S. Recent data in a general population over 40 demonstrated an incidence of PAD defined by ankle brachial index (ABI) of 4.3%. Another study of over 3000 patients, mean age 59, demonstrated a prevalence of 3.9%. The prevalence is age-dependent, rising to 14.5% in those over 70. In populations at risk including diabetics or smokers, the incidence is nearly 30%. Standard cardiovascular (CV) risk factors are also risks for PAD, especially smoking, diabetes, hypertension, African-American race and chronic kidney disease. The annual rate of CV events including myocardial infarction, stroke, and CV death is 5-7%. The adjusted risk of dying of a CV event is 2-fold higher than those without PAD. Magnetic resonance imaging (MRI) methods can accurately quantify atherosclerotic plaque in the superficial femoral artery (SFA) in patients with PAD. These measures can be performed rapidly and reproducibly with an intraclass correlation of 0.997 for intraobserver reproducibility, 0.987 for intraobserver, and 0.996 for test-retest reproducibility, Plaque regression with statins have been shown using these techniques in PAD. Alirocumab is a PCSK9 inhibitor that effectively reduces LDL cholesterol up to 70% in patients on statins or intolerant to statins. This injectable agent has proven safe and well-tolerated, but has not yet been studied specifically in patients with peripheral arterial disease.The study will be a double blind, placebo-controlled, randomized study of Alirocumab vs. placebo in 54 patients with PAD. Baseline visit: Informed consent will be signed. Vital signs will be taken and blood drawn fasting for baseline values. A MRI would be performed with black blood imaging of the SFA of both legs. Approximately 10-15 cm of each leg would be covered, using a specifically designed surface coil (Machnet, Leiden, NL). The imaging would start at the bifurcation of the common femoral and proceed distally. The pulse sequence used will be a black blood turbo spin echo proton density weighted sequence with 3mm slice thickness and 3mm gaps that will be subsequently interleaved. A single slice with an extensive amount of plaque will be chosen for imaging of plaque characteristics including T1- and T2-W imaging. Finally, a calf muscle perfusion study will be performed in the leg that is most symptomatic and/or has the lowest ABI in the absence of claudication symptoms. The calf will be wrapped in a flexible surface coil in a 3T scanner. Subjects will be placed supine in the MR scanner with the calf at the magnet isocenter. A thigh cuff will be inflated up to 250 mmHg for 5 min. Arterial spin labeling images of the mid-calf will be obtained immediately after release of the cuff.Regions of interest will be drawn on the relative blood flow maps corresponding to calf muscle groups to measure perfusion in ml/min/100g. Randomization: The study statistician will do a block randomization and let the pharmacy know. Patients in the treatment group will begin treatment with alirocumab or matching placebo, 150 mg subcutaneously every 2 weeks. Treatment will continue for 26 treatments or 1 year. Final Visit: This will be a repeat of the initial visit with vital signs, blood draw for lipid panel, and repeat MRI with the exact same protocol as on the initial visit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Arterial Disease
Keywords
MRI, PCSK9 inhibition, LDL cholesterol

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Alirocumab
Arm Type
Experimental
Arm Description
Alirocumab 150mg SQ every 2 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Matched placebo
Intervention Type
Drug
Intervention Name(s)
Alirocumab
Other Intervention Name(s)
Praluent
Intervention Description
150mg SQ every 2 weeks
Intervention Type
Drug
Intervention Name(s)
Matching placebo
Intervention Description
SQ every 2 weeks
Primary Outcome Measure Information:
Title
Change in superficial femoral plaque volume (summed from both legs)
Description
Measured by black blood MRI, expressed in cm3
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Change in calf muscle perfusion in the most symptomatic leg
Description
Measured by arterial spin labeling MRI, expressed in ml/min/100g
Time Frame
1 year
Title
Change in plaque characteristics
Description
% lipid in one slice from each leg
Time Frame
1 year
Title
Change in 6-minute walk test
Description
expressed in feet
Time Frame
1 year
Title
Change in LDL cholesterol
Time Frame
1 year
Title
Change in high sensitivity c-reactive protein
Time Frame
1 year
Title
Change in fibrinogen
Time Frame
1 year
Title
Change in lipoprotein (a)
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 35-85 Clinical diagnosis of peripheral arterial disease Ankle brachial index of 0.4-0.9 Either on statin for at least 6 months or statin intolerant. The statin used should be a high potency statin (Crestor, Lipitor) or high dose of a lower potency statin (e.g. Zocor 40-80mg, Pravachol 40-80 mg) Exclusion Criteria: rest pain critical limb ischemia known or planned stent in the SFA known occlusion of the SFA planned revascularization within the next year inability to lie flat known contraindications to MRI including pacemaker, implantable cardioverter defibrillators, certain intracranial aneurysm clips, claustrophobia pregnancy known allergy to alirocumab
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christopher M Kramer, MD
Organizational Affiliation
University of Virginia Health System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern University
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
University of Virginia Health System
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22908
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
37093712
Citation
Rrapo-Kaso E, Loffler AI, Petroni GR, Meyer CH, Walker M, Kay JR, DiMaria JM, Domanchuk K, Carr JC, McDermott MM, Kramer CM. Alirocumab and plaque volume, calf muscle blood flow, and walking performance in peripheral artery disease: A randomized clinical trial. Vasc Med. 2023 Aug;28(4):282-289. doi: 10.1177/1358863X231169324. Epub 2023 Apr 24.
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A Trial of Alirocumab and Plaque Regression in Peripheral Arterial Disease

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