PCSK9 Inhibitors in the Progression of Aortic Stenosis
Primary Purpose
Aortic Valve Stenosis
Status
Unknown status
Phase
Phase 2
Locations
Korea, Republic of
Study Type
Interventional
Intervention
PCSK9 Inhibitor [EPC]
Placebos
Sponsored by
About this trial
This is an interventional prevention trial for Aortic Valve Stenosis focused on measuring aortic valve stenosis, PCSK9 inhibitor
Eligibility Criteria
Inclusion Criteria:
- The patient agrees to participate in this study by signing the informed consent form. Alternatively, a legally authorized patient representative may agree to the patient's participation in this study and sign the informed consent form.
- The patient has a working diagnosis of aortic stenosis (mild to moderate), and has fair treatment compliance.
Exclusion Criteria:
- Age under 19 years old
- Hypersensitivity to PCSK9 inhibitor
- LDL cholesterol < 70mg/dL at baseline
- Poor treatement compliance (The patient will need to visit the out-patient clinic every 2-weeks for medication)
- Positive pregnancy test or is known to be pregnant
- Any other reason the investigator deems the subject to be unsuitable for the study (e.g., Active malignant tumor, Any life-threatening condition with life expectancy less than 6months, etc.)
- Any clinically significant abnormality identified at the screening visit, physical examination, laboratory tests, or electrocardiogram which, in the judgment of the investigator, would preclude safe completion of the study
Sites / Locations
- Seoul National University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
PCSK9 inhibitor
Placebo
Arm Description
Patients will receive bi-weekly PCSK9 inhibitor .
Patients will receive bi-weekly placebo.
Outcomes
Primary Outcome Measures
Progression of the Calcium score measured by cardiac CT (Agatston score) and by NaF PET
Calcium score progression in the PCSK9 inhibitor group and placebo group
Secondary Outcome Measures
Efficacy of inhibition in calcium score progression (Agatston score) by the presence of Lp(a) SNPs
Mean change in Lp(a) levels between treatment arms
Lp(a) levels will be measured in blood chemistry
Mean change in lipid panel (LDL, HDL, TG, Cholesterol) level
Lipid panels will be measured in blood chemistry
Aortic valve area measured by echocardiography
Aortic valve peak velocity measured by echocardiography
Any death event
Any cardiac death event
Any myocardial infarction event
Any revascularization for coronary artery disease
Full Information
NCT ID
NCT03051360
First Posted
January 23, 2017
Last Updated
February 8, 2017
Sponsor
Seoul National University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03051360
Brief Title
PCSK9 Inhibitors in the Progression of Aortic Stenosis
Official Title
Proprotein Convertase Subtilisin Kexin Type 9 Inhibitor in Aortic Stenosis
Study Type
Interventional
2. Study Status
Record Verification Date
February 2017
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2017 (Anticipated)
Primary Completion Date
December 31, 2019 (Anticipated)
Study Completion Date
January 1, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Hospital
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
Investigators plan evaluate whether PCSK9 inhibitors, a medication that can lower lipoprotein(a) and control dyslipidemia, can inhibit the progression of aortic stenosis, through a randomized controlled trial.
Detailed Description
Aortic valve disease is the most common form of heart valve disease and is a major burden to society. Aortic valve disease is also expected to become more prevalent with the aging. Among aortic diseases, 'aortic stenosis (AS)', which is a narrowing of the aortic valve, and leads to symptoms of heart failure and sometimes death.
For treatment of AS, the valve in replaced in a surgical to percutaneous method. Regardless of the method, valve replacement has its potential costs and complications that is an important issue that needs to be solved. Therefore, controlling the progression of AS and increasing the efficacy of medical therapy before valvular replacement is needed, is an important medico-social problem.
Regarding the pathophysiology of AS, an elevation of lipoprotein(a) and dyslipidemia have been reported to be associated with the progression of cardiovascular calcification.
PCSK9 inhibitors, which is a medication that can control both lipoprotein(a) and dyslipidemia may be a effective medication to control the progression of AS.
Therefore, investigators will perform a randomized control trial, to compare the effect of PCSK9 inhibitors vs. placebo in its influence to AS progression.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aortic Valve Stenosis
Keywords
aortic valve stenosis, PCSK9 inhibitor
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Prospective, Double blind, Multi-center, Randomized clinical trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
140 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
PCSK9 inhibitor
Arm Type
Active Comparator
Arm Description
Patients will receive bi-weekly PCSK9 inhibitor .
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Patients will receive bi-weekly placebo.
Intervention Type
Drug
Intervention Name(s)
PCSK9 Inhibitor [EPC]
Intervention Description
Patients will receive PCSK9 inhibitor by a biweekly injection
Intervention Type
Drug
Intervention Name(s)
Placebos
Intervention Description
Patients will receive Placebo by a biweekly injection
Primary Outcome Measure Information:
Title
Progression of the Calcium score measured by cardiac CT (Agatston score) and by NaF PET
Description
Calcium score progression in the PCSK9 inhibitor group and placebo group
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Efficacy of inhibition in calcium score progression (Agatston score) by the presence of Lp(a) SNPs
Time Frame
2 years
Title
Mean change in Lp(a) levels between treatment arms
Description
Lp(a) levels will be measured in blood chemistry
Time Frame
2 years
Title
Mean change in lipid panel (LDL, HDL, TG, Cholesterol) level
Description
Lipid panels will be measured in blood chemistry
Time Frame
2 years
Title
Aortic valve area measured by echocardiography
Time Frame
2 years
Title
Aortic valve peak velocity measured by echocardiography
Time Frame
2 years
Title
Any death event
Time Frame
2 years
Title
Any cardiac death event
Time Frame
2 years
Title
Any myocardial infarction event
Time Frame
2 years
Title
Any revascularization for coronary artery disease
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
The patient agrees to participate in this study by signing the informed consent form. Alternatively, a legally authorized patient representative may agree to the patient's participation in this study and sign the informed consent form.
The patient has a working diagnosis of aortic stenosis (mild to moderate), and has fair treatment compliance.
Exclusion Criteria:
Age under 19 years old
Hypersensitivity to PCSK9 inhibitor
LDL cholesterol < 70mg/dL at baseline
Poor treatement compliance (The patient will need to visit the out-patient clinic every 2-weeks for medication)
Positive pregnancy test or is known to be pregnant
Any other reason the investigator deems the subject to be unsuitable for the study (e.g., Active malignant tumor, Any life-threatening condition with life expectancy less than 6months, etc.)
Any clinically significant abnormality identified at the screening visit, physical examination, laboratory tests, or electrocardiogram which, in the judgment of the investigator, would preclude safe completion of the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hyo-Soo Kim, MD, PhD
Phone
+82-2- 2072-2226
Email
hyosoo@snu.ac.kr
First Name & Middle Initial & Last Name or Official Title & Degree
Jeehoon Kang, MD
Phone
+82-10-2416-2406
Email
medikang@gmail.com
Facility Information:
Facility Name
Seoul National University Hospital
City
Seoul
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hyo-Soo Kim, MD, PhD
Phone
+82-2- 2072-2226
Email
hyosoo@snu.ac.kr
First Name & Middle Initial & Last Name & Degree
Jeehoon Kang, MD
Phone
+82-10-2416-2406
Email
medikang@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
PCSK9 Inhibitors in the Progression of Aortic Stenosis
We'll reach out to this number within 24 hrs