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Efficacy and Safety of Allogeneic Mesenchymal Precursor Cells (Rexlemestrocel-L) for the Treatment of Heart Failure.

The primary objective of this study is to determine whether transendocardial delivery of allogeneic human bone marrow-derived mesenchymal precursor cells (MPCs [rexlemestrocel-L]) is effective in the treatment of chronic heart failure (HF) due to left ventricular (LV) systolic dysfunction.

Stanford is currently accepting patients for this trial.

Stanford Investigator(s):

Intervention(s):

  • other: Sham Comparator
  • biological: Allogeneic Mesenchymal Precursor Cells (MPCs)

Eligibility


Inclusion Criteria:

   - The patient is 18 to 80 years of age, inclusive; both men and women will be enrolled.

   - The patient has a diagnosis of chronic HF of ischemic or nonischemic etiology for at
   least 6 months

   - The patient is on stable, optimally tolerated dosages of HF therapies including
   beta-blockers (approved for country-specific usage), angiotensin-converting enzyme
   (ACE) inhibitors or angiotensin-receptor blockers (ARBs), and/or aldosterone
   antagonists, without change in dose for at least 1 month before study intervention

   - The patient is on a stable, outpatient, oral diuretic dosing regimen in which the
   patient remains clinically stable during screening.

   - Other Criteria apply, please contact the investigator

Exclusion Criteria:

   - The patient has NYHA Functional Class I or Functional Class IV symptoms.

   - Other Criteria apply, please contact the investigator

Ages Eligible for Study

18 Years - 80 Years

Genders Eligible for Study

All

Now accepting new patients

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Recruiting