ST Segment Elevation Myocardial Infarction (STEMI) Clinical Trial
Official title:
A PHASE IIa, DOUBLE-BLINDED, MULTI-CENTER, RANDOMIZED STUDY TO ASSESS THE SAFETY,TOLERABILITY, AND PRELIMINARY EFFICACY OF A SINGLE INTRAVENOUS DOSE OF ALLOGENEIC MESENCHYMAL BONE MARROW CELLS TO SUBJECTS WITH ST SEGMENT ELEVATION MYOCARDIAL INFARCTION (STEMI)
The purpose of this study is to assess the safety and tolerability of human allogeneic mesenchymal bone marrow cells (aMBMC) administered intravenously to subjects with ST Segment Elevation Myocardial Infarction (STEMI).
Cardiovascular disease (CVD) remains a leading cause of morbidity and mortality despite
continuing advances in various treatment options. In developed countries, ischemic heart
disease causes more than 50% of all cardiovascular deaths. It is estimated that one in three
or approximately 80 million American adults have one or more types of CVD, with
approximately 38.1 million of those estimated to be 60 years of age or older. The data was
extrapolated to the United States population in 2006 from National Health and Nutrition
Examination Survey (NHANES) 2005-2006 data.
Mortality data show CVD as the underlying cause of death (including congenital
cardiovascular defects) accounting for 35.3% (864,480) of all 2,448,017 deaths in 2005, or
one of every 2.8 deaths in the United States. CVD total deaths (1,372,000 deaths in 2005)
accounted for about 56% of all deaths in 2005. Nearly 2,400 Americans die of CVD each day,
an average of one death every 30 seconds. CVD claims about as many lives each year as
cancer, chronic lower respiratory diseases, accidents, and diabetes mellitus combined
(NCHS).
Stem cell transplantation has the potential to repair and improve cardiac function, thus
helping to significantly decrease morbidity and mortality rates. Preclinical data from a
variety of animal studies demonstrated the capacity for skeletal myoblasts to engraft, form
myotubules, and enhance cardiac function after transplantation into infarcted myocardium.
The underlying sequela of the post infarcted left ventricle often includes massive damage to
the cardiomyocyte. The left ventricle remodeling (dilation) and dysfunction is thought to be
irreversible. The development of treatments that will regenerate its musculature and
vascular components is now considered a main therapeutic challenge. Preliminary human
studies focusing on subjects with ischemic heart disease have demonstrated successful
myoblast transplantation into the post infarction scar. Another study demonstrated the
benefits of stem cell therapy on ventricular function and profusion. Dib et. al.,
demonstrated the survival, feasibility, and safety of autologous myoblast transplantation
and suggests that stem cell transplantation offers a potential therapeutic treatment for
end-stage heart disease.
Allogeneic mesenchymal stem cells have been used in a number of clinical trials for
different indications. These clinical trials demonstrated the safety of allogeneic
mesenchymal stem cell treatment. Allogenic mesenchymal bone marrow cells can be isolated
from bone marrow. They are the primary cells used in tissue engineering expressing multiple
cell types. Tissue engineering is very promising, generating hope that reconstruction of
organs and repair diseased and damaged tissue may be possible.
There are two major types of aMBMC, hematopoetic (mononuclear) and stromal MSCs. Stromal
MBMC, the cell type to be used in this study, proved to be more effective in reestablishing
profusion as they secreted additional cytokine factors associated with angiogenesis. The
multilineage potential of stromal MSCs, their ability to elude detection by the host immune
system and even down regulate T-cell response allows for allogeneic multiple stem cell
therapeutic use.
Occlusion of the left main or left anterior descending artery causes irreversible injury to
the cardiomyocytes in as little as 20 minutes. The goal of therapy in ischemic
cardiomyopathy is to limit damage in the following areas:
- Limit infarct size
- Prevent reperfusion injury
- Prevent excessive fibrosis
- Reestablish function of hibernating cardiomyocytes in peripheral zone area.
- Reestablish angiogenesis/vasculogenesis
- Preserve wall motion (prevent arrhythmia and functional contractile deterioration)
- Prevent post infarct ventricular remodeling and left ventricular dilation It is well
accepted that dilated cardiomyopathy mortality rates are 50% within 5 years of
diagnosis. If we can preserve and restore cardiac function as measured by ejection
fraction, preserving left ventricular integrity would increase subject quality of life
as well as longevity.
An IV study administering adult allogeneic mesenchymal stem cells (MSC) to 53 subjects
following AMI showed excellent safety, reduction in arrhythmias, improvement in functional
status and increased ejection fraction. The availability of "off the shelf" allogeneic stem
cells will allow for an easily adjustable dose (getting enough cells in the autologous model
is often a problem) for each individual subject. The ease of IV administration will make
stem cell therapy more cost effective and safer to administer than the current catheter
models. This study protocol will expand on the safety and efficacy of aMBMC in subjects
suffering from ischemic cardiomyopathy.
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT02429271 -
A Multicenter Trial to Assess the MIcrovascular Integrity and Left Ventricular Function Recovery After Clopidogrel or TicagrelOr Administration, in Patients With STEMI Treated With Thrombolysis - The 'MIRTOS' Study
|
Phase 3 |