Use of Adult Autologous Stem Cells in Treating People Who Have Had a Heart Attack (The TIME Study)

More than 1 million Americans suffer a heart attack each year, resulting in about a 38% mortality rate. Although current treatments are able to stabilize the condition of the heart, none is able to restore heart function as it was prior to the heart attack. The permanent damage to the heart can lead to more severe problems, such as heart failure and irregular heartbeat, making the discovery of treatments to improve heart function after a heart attack important. Adult stem cells, which are immature cells that can become many different types of cells, may offer a potential means of reversing or preventing permanent damage caused by a heart attack. These specialized cells may have the ability to promote blood vessel growth, prevent cell death, and transform themselves into a number of tissues, including muscle. Recent studies have shown promise in using adult stem cells from bone marrow to reverse damage to the heart muscle caused by a heart attack, but more research is needed to assess the safety and effectiveness of stem cell use and to discover the best time to administer treatment. This study will evaluate the safety and effectiveness of placing adult stem cells into injured heart muscle for improving heart function in people who have had a recent heart attack and a PCI. Additionally, this study will help determine the best time to insert stem cells after a heart attack.

Participation in this study will last 24 months. All participants will first undergo baseline assessments that will include a medical history, a physical exam, an electrocardiogram (ECG), blood draws, an echocardiogram, and a magnetic resonance imaging (MRI) test. Participants will then be assigned randomly to receive stem cells or placebo either 3 or 7 days after their heart attack. The morning of the stem cell or placebo infusion, participants will undergo a blood draw and a bone marrow aspiration procedure of the hip bone to collect the stem cells. Later the same day, either stem cells or placebo will be infused through a catheter and into the damaged area of the heart.

For the first 24 hours following the infusion, participants will be asked to wear a small ECG machine called a Holter monitor. Participants will also be asked to record their temperature twice a day for a month after the infusion. Participants will return for follow-up visits at Months 1, 3, 6, 12, and 24 and will repeat many of the baseline assessments.

Inclusion criteria

• Patients at least 21 years of age
• Patients with first acute MI with successful primary percutaneous coronary intervention (PCI) in an artery at least 2.5 mm in diameter within 24 hours of onset of symptoms.
• No contraindications to undergoing cell therapy procedure within three to seven days following AMI and PCI.
• Hemodynamic stability as defined as no requirement for IABP, inotropic or blood pressure supporting medications.
• Ejection fraction following reperfusion with PCI <=45% as assessed by echocardiography.
• Consent to protocol and agree to comply with all follow-up visits and studies.
• Women of child bearing potential willing to use an active form of birth control.

Exclusion criteria

Patients will be excluded from the study if they meet any of the following conditions:

• History of sustained ventricular arrhythmias not related to their AMI (evidenced by previous holter monitoring and/or medication history for sustained ventricular arrhythmias in patient's medical chart).
• Require CABG or PCI due to the presence of residual coronary stenosis >70% luminal obstruction in the non-infarct related vessel (Additional PCI of non-culprit vessels may be performed prior to enrollment).
• History of any malignancy within the past five years excluding non-melanoma skin cancer or cervical cancer in-situ.
• History of chronic anemia (hemoglobin (Hb) <9.0 mg/dl).
• History of thrombocytosis (platelets >500k).
• History of thrombocytopenia in the absence of recent evidence that platelet counts are normal
• Known history of elevated INR (PT) or PTT.
• Life expectancy less than one year.
• History of untreated alcohol or drug abuse.
• Currently enrolled in another investigational drug or device trial
• Previous CABG.
• Previous MI resulting in LV dysfunction (LVEF <55%)
• History of stroke or transient ischemic attack (TIA) within the past six months.
• History of severe valvular heart disease (aortic valve area <1.0 cm2 or >3+ mitral regurgitation).
• Pregnancy or breast feeding
• Subjects with a known history of HIV, or has active hepatitis B,active hepatitis C, or active TB
• Patients with active inflammatory or autoimmune disease on chronic immuno-suppressive therapy.
• Contraindications to cMRI.
• Previous radiation to the pelvis with white blood cell count (WBC) and platelet counts below hospital specific normal values.
• Women child bearing potential not willing to practice an active form of birth control.
• Chronic liver disease that might interfere with survival or treatment with cell therapy.
• Chronic renal insufficiency as defined by a creatinine ≥ 2.0 mg/dL or requires chronic dialysis.