Safety Study of Allogeneic Mesenchymal Precursor Cells (MPCs) in Subjects With Recent Acute Myocardial Infarction

Status unconfirmed · Phase 1/Phase 2

Conditions studied: Myocardial Infarction

In brief

Primary Objective The primary objective of this study is to evaluate the safety and feasibility of transendocardial injection using the Cordis Biosense NogaStarTM Mapping Catheter with the Biosense MyostarTM Left Ventricular Injection Catheter of 25 M, 75 M, and 150 M allogeneic mesenchymal precursor cells (MPCs) in subjects with AMI. SecondaryObjective The secondary objectives are to explore functional efficacy for subsequent study design, as well as late-term dose related tolerance, by: * Evaluating the effect of allogeneic MPCs on exploratory efficacy endpoints related to cardiac function on Days 90, 180, and 1 year * Evaluating the change from baseline in the Medical Outcome Study Short Form (SF-36), Kansas City Cardiomyopathy Questionnaire, Seattle Angina Questionnaire, and the New York Heart Association Classification at 30 days, 3 and 6 months, and 1, 2, and 3 years * Evaluating follow-up safety through Day 360 * Providing preliminary data to support dose selection for future studies

Key facts

Study ID: NCT00555828
Run by: Angioblast Systems
People needed: 25
Starts: 2008-03-01
Expected to finish: 2013-12-01
Last updated by the study team: 2010-02-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Age 18 years or older.
An ST-elevation MI (STEMI) within 2 to 10 days of study enrollment. The STEMI must be documented by ECG with ST-segment elevation >1 mm in at least 2 contiguous precordial leads or in at least 2 adjacent limb leads. If there is a history of a previous AMI prior to the qualifying MI, then there must be a documented EF ≥ 50% by 2D echocardiogram within 12 months of enrollment.
Successful percutaneous revascularization with Thrombolysis in Myocardial Infarction (TIMI)-3 flow of the infarct-related artery.
A baseline 2D echocardiogram with EF ≥ 30 and ≤ 50% following PCI.
Creatinine level ≤ 1.5mg/dL within 24 hours of study procedure.
Hematocrit ≥ 30% within 24 hours of study procedure.
White Blood Cell count < 20k/mm3 within 24 hours of study procedure.
Platelet count ≥ 100k/mm3 within 24 hours of study procedure.
INR ≤ 1.7 within 24 hours of study procedure.
Total bilirubin <3 mg/dL, albumin >2.8 g/dL, aspartate aminotransferase(AST) ≤ 2.5x the upper limit of normal, gamma glutamyltranspeptidase (GGT) ≤ 1.5 x the upper limit of normal.
If the subject or partner is of childbearing potential, he or she must be willing to use adequate contraception (hormonal or barrier method or abstinence) from the time of screening and for a period of at least 16 weeks after surgery.
Female subjects of childbearing potential must have a negative serum pregnancy test at screening (within 2 weeks of enrollment) and a negative serum or urine pregnancy test on the day of cell implantation.
Willing and able to understand, sign, and date the Informed Consent Form (ICF).
Must be willing to return for required follow-up visits.
Must be able to follow postoperative management program.

You may not qualify if…

Subject is hemodynamically unstable at Day 5 post-AMI as demonstrated by any of the following:
Killip Class 4 indicative of cardiogenic shock.
Requirement of intra-aortic balloon pump or IV inotropic support for the maintenance of mean arterial blood pressure ≥ 60 mmHg.
Sustained ventricular tachycardia as demonstrated by QRS complexes wider than 120 msec, lasting >30 secs, and >100 bpm occurring >48 hours following PCI without any identifiable, reversible cause (ie, electrolyte imbalance).
Further revascularization planned for the next 30 days.
Chronic atrial fibrillation.
A wall thickness in the target region <8 mm as determined by 2D echocardiography(the target region is defined at the time of NOGA® mapping).
An LV thrombus.
Severe peripheral vascular disease precluding femoral artery access as determined at time of original catheterization.
Aortic stenosis as determined as valve area less than 1 cm2 that prohibits catheter access to the LV.
Echocardiographic evidence of hypertrophic cardiomyopathy indicating heart muscle thickness >15 mm.
Human immunodeficiency virus (HIV)
Serum glucose level ≥ 400 mg/dl within 24 hours of study procedure
Serum glucose level 300-400 mg/dl and presence of urine ketones within 24 hours of study procedure.
Claustrophobic, or with medical conditions or contradictions that impede performing baseline MRI study.
An active uncontrolled infection.
A prosthetic aortic valve.
Presence of ≥ 20% anti-HLA antibody titers and/or having antibody specificities to donor HLA antigens.
A current or prior history within the last 3 years of neoplasm (excluding basal cell) and/or any active neoplasm within the last 24 months.
A known hypersensitivity to dimethyl sulfoxide (DMSO), murine and/or bovine products.
Pregnancy or breastfeeding.
Imprisoned at the time of enrollment.
A treatment and/or an uncompleted follow-up treatment of any investigational therapy within 6 months before implantation surgery and intent to participate in any other investigational drug or cell therapy study during the 3-year follow-up period of this study.
Active participation in other research therapy for cardiovascular repair/regeneration.
A prior recipient of stem precursor cell therapy for cardiac repair.

Where it is running

University of Minnesota/Minneapolis Heart Institute — Minneapolis, Minnesota, United States (enrolling)
Texas Heart Institute/St. Luke's Hospital — Houston, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.