Effect of Evolocumab on Coronary Plaque Characteristics: a Multimodality Imaging Study

Who is this study for? Adult patients with coronary artery disease
What treatments are being studied? Evolocumab
Status: Completed
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

The aim of the study is to assess the effect of evolocumab on coronary plaque morphology using intravascular imaging and gene expression analysis of peripheral blood mononuclear cells (PBMC) in patients with stable CAD on maximally tolerated statin therapy. The study combines multi-modality intravascular imaging approaches and transcriptomic based machine learning algorithms to uncover molecular mechanisms responsible for the beneficial changes in atherosclerotic lesions of patients treated with evolocumab. The primary end-points are the changes from baseline to follow-up in (1) the minimal fibrous cap thickness (FCT) assessed by optical coherence tomography (OCT) and (2) maxLCBI4mm assessed by near-infrared spectroscopy (NIRS) after 26 weeks of evolocumab. The secondary endpoints are the changes in (1) the maximal lipid arc, lipid length, lipid volume index, macrophage accumulation and calcification by OCT; (2) PAV and TAV defined by intravascular ultrasound (IVUS) and (3) Changes in PBMC gene expression.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Men or women aged 18 years or older at screening who signed written Informed Consent

• Patients with coronary artery disease undergoing cardiac catheterization and PCI for a target lesion and also have a non-obstructive lesion (30-50% stenosis) identified by angiography

• Patients who are not candidates for PCI or CABG currently or over the next 12 months, in the opinion of the investigator

• Patients treated with statins for at least 4 weeks with LDL-C level ≥ 80 mg/dL for low- or moderate -intensity statin use and ≥ 60 mg/dL for high-dose statin. Patients with history of statin intolerance and LDL-C ≥ 100 mg/dL.

• Angiographic criteria: 30-50% reduction of lumen diameter in addition to the target lesion accessible by the OCT catheter. The target segment should not have a history of percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG), and may not be a bypass graft.

• OCT criteria: target segment should have a lipid-rich plaque with lipid arc \>90° and fibrous cap thickness ≤120 µm.

• Women of childbearing potential must agree to be on an acceptable method of birth control/contraceptive

Locations
United States
New York
Mount Sinai Hospital
New York
Time Frame
Start Date: 2021-05-04
Completion Date: 2023-11-06
Participants
Target number of participants: 137
Treatments
Experimental: Treatment
Evolocumab subcutaneously administered 140 mg every 2 weeks for 26 weeks
Related Therapeutic Areas
Sponsors
Leads: Annapoorna Kini

This content was sourced from clinicaltrials.gov