Status:
WITHDRAWN
Safety and Efficacy Study of Gene Therapy for Acute Myocardial Infarction in Korea
Lead Sponsor:
Helixmith Co., Ltd.
Conditions:
Ischemic Heart Disease
Acute Myocardial Infarction
Eligibility:
All Genders
19-75 years
Phase:
PHASE2
Brief Summary
The purpose of this study is to evaluate the safety and clinical efficacy of VM202RY injected via transendocardial route using C-Cathez® catheter (Celyad, S.A., Belgium) in subjects with AMI. * Stage...
Detailed Description
Ischemic heart disease, a condition in which narrowed or blocked coronary arteries lead to ischemia in myocardium, is a group of disease that include: angina and myocardial infarction. Acute myocardi...
Eligibility Criteria
Inclusion
- Age ≥ 19 years to ≤ 75 years
- Patients who underwent percutaneous coronary intervention (PCI) for the anterior wall infarction of left ventricle and had the elapsed time of 30 ± 2 days from the PCI, regardless of success or failure of myocardial revascularization in the anterior wall
- Patients with \> 20% to ≤ 45% of left ventricular ejection fraction via trans-thoracic echocardiography within 7 days prior to the study drug or placebo injection
- Left ventricular wall thickness ≥ 8 mm via trans-thoracic echocardiography (however, the subject shall be included if 50% or greater of the left ventricular anterior wall is ≥8mm or injection site other than the left ventricular anterior wall is ≥ 8mm.)
- If female of childbearing potential, negative urine pregnancy test at screening and using acceptable method of birth control during the study; if male, using barrier method of birth control during study
- Be capable of understanding and complying with the protocol and signing the informed consent document prior to being subjected to any study related procedures.
Exclusion
- Severe systolic heart failure, NYHA Class III or IV
- New York Heart Association (NYHA) functional class IV
- History of recurrent ventricular tachycardia or cariogenic shock following PCI
- Stroke or transient ischemic attack (TIA) within 180 days
- Uncontrolled hypertension defined as systolic blood pressure ≥ 180 mmHg or diastolic ≥ 110 mmHg at screening and/or on the day of study drug or placebo injection
- Sustained ventricular tachyarrhythmia or recurrent ventricular tachycardia
- Implantation of automatic implantable cardioverter defibrillator (AICD)
- On extracorporeal membrane oxygenator (ECMO)
- History of ventricular fibrillation after PCI
- Permanent pacemaker implantation (temporary pacemaker may be enrolled)
- Subjects with aortic stenosis of moderate or greater degree, or with prosthetic aortic valve who may not be appropriate to use the C-CATHez® catheter due to the risk of injury during the interventional procedure through the valve
- Atherosclerotic or other disease of the aorto-iliac system that would impede the safe passage of the C-CATHez®
- Subjects with any serious comorbidities that the investigators deemed to be inappropriate to be enrolled
- Patients with a recent history (\< 5 years) of, or new screening finding of malignant neoplasm except basal cell carcinoma or squamous cell carcinoma of the skin (if excised and no evidence of recurrence); patients with family history of colon cancer in any first degree relative are excluded unless they have undergone a colonoscopy in the last 12 months with negative findings
- Elevated prostate-specific antigen (PSA) despite not having prostate cancer history
- Ophthalmologic conditions pertinent to proliferative retinopathy or conditions that preclude standard ophthalmologic examination Diagnosis of proliferative retinopathy or conditions that preclude standard ophthalmologic examination
- Subjects currently receiving immunosuppressive medications, chemotherapy, or radiation therapy
- Active infectious disease and/or positive Human Immunodeficiency Virus (HIV) or Human T-Cell lymphotropic viruses (HTLV) at screening
- Active Hepatitis B or C infection as determined by Hepatitis B surface antibody (HBsAb), Hepatitis B core antibody (Immunoglobulin G and Immunoglobulin M; HBcAb), Hepatitis B surface antigen (HBsAg) and Hepatitis C antibodies (Anti-HCV) at screening
- Specific laboratory values at screening including
- Hemoglobin ≤ 9.0 g/dL, white blood cell (WBC) \< 3,000 cells/μl, platelet count \< 75,000/mm3
- Creatinine \> 2.0 mg/dL
- Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) \> 3 x upper limit of normal (ULN)
- Any other clinically significant lab abnormality which in the opinion of the investigator should be exclusionary
- Subjects requiring \> 100 mg daily of acetylsalicylic acid (ASA); subjects may be enrolled if willing/able to switch to ≤ 100 mg daily of ASA or to another medication
- Subjects regularly taking cyclooxygenase (COX)-2 inhibiting drug(s) or non-specific COX-1/COX-2 inhibiting drugs, or high dose steroids (except inhaled steroids); subjects may be enrolled if willing/able to undergo medication wash-out prior to the first dosing and to refrain from taking these drugs for the duration of the study, and also if the subject is temporarily taking NSAID (non-steroidal anti-inflammatory drug) temporarily (≤ 7 days)
- Patients that have undergone enhanced external pulsation (EECP) treatment within the last 6 months
- Pregnancy or lactation
- Severe comorbidity associated with a reduction of life expectancy of less than 1 year
- Exposure to any previous experimental angiogenic therapy and/or myocardial laser therapy; or therapy with another investigational drug within 180 days of enrollment or participation in any concurrent study that may confound the results of this study
- Major psychiatric disorder in the past 6 months
- Known drug or alcohol dependence or any other factors which will interfere with the study conduct or interpretation of the results or who in the opinion of the investigator are not suitable to participate
- Deemed to be in unsuitable condition by the study investigator
Key Trial Info
Start Date :
January 25 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 20 2019
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT03404024
Start Date
January 25 2018
End Date
August 20 2019
Last Update
September 25 2025
Active Locations (4)
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1
GangNeung Asan Hospital
Gangneung, South Korea
2
Chonnam National University Hospital
Gwangju, South Korea
3
Ewha Womans University Medical Center
Seoul, South Korea
4
KyungHee University Medical Center
Seoul, South Korea