TEVA C41750/3100 (DREAM-HF) Study
Condition: Heart failure
Eligibility
Key Inclusion Criteria
- 18 to 80 years of age
- Diagnosis of chronic heart failure of ischemic or non-ischemic etiology
- On stable, optimally tolerated dosages of heart failure therapies
- On a stable, outpatient, oral diuretic dosing regimen
- Not a candidate for either percutaneous coronary intervention or coronary artery bypass graft surgery
Key Exclusion Criteria
- New York Heart Association Functional Class I or Functional Class IV symptoms
- Acute myocardial infarction within one month before screening procedures
- Unstable angina pectoris within one month before screening procedures
- Peri-/postpartum cardiomyopathy
- Ischemic or hemorrhagic stroke within three months prior to enrollment
Full Study Name
A Double-Blind, Randomized, Sham-Procedure-Controlled, Parallel-Group Efficacy and Safety Study of Allogeneic Mesenchymal Precursor Cells (CEP-41750) in Patients with Chronic Heart Failure Due to Left Ventricular Systolic Dysfunction of Either Ischemic or Nonischemic Etiology (IRB no. 35633)
Summary
This research study is designed to test the investigational use of CEP-41750 (mesenchymal precursor cells) in patients with chronic heart failure. Researchers will examine whether injecting the cells into heart muscle with a specific type of needle can help restore heart muscle function.
The study will compare CEP-41750 to the standard treatment (standard of care for heart failure). Participants will receive either CEP-41750 or undergo a partial procedure and will not receive CEP-41750.
Phase
Phase III
Principal Investigator
David Chang, MD
Timothy Henry, MD
Co-Investigators
Michele Hamilton, MD
Jon Kobashigawa, MD
Jaime Moriguchi, MD
Antoine Hage, MD
Jignesh Patel, MD, PhD
Michelle Kittleson, MD, PhD
Lawrence Czer, MD
Babak Azarbal, MD
Dael Geft, MD
Mamoo Nakamura, MD
Contact
Tracey Early
310-423-1231
tracey.early@cshs.org
Maria Thottam
310-248-7136
maria.thottam@cshs.org