A Study to Evaluate the Effectiveness and Safety of Human Bone Marrow Derived Stem Cells (CEP-41750) for the Treatment of Chronic Heart Failure.

Overview

About this study

The primary objective of this study is to determine whether transendocardial delivery of human bone marrow-derived stem cells (CEP-41750) is effective in the treatment of chronic heart failure due to LV systolic dysfunction.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria

  • 18 to 80 years of age, inclusive
  • Men or women
  • Has a diagnosis of chronic HF of ischemic or nonischemic etiology for at least 6 months
  • 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
  • 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

  • Has NYHA Functional Class I or Functional Class IV symptoms
  • Other criteria apply, please contact the investigator

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

Robert Scott, M.D., Ph.D.

Closed for enrollment

More information

Publications

Publications are currently not available
.
CLS-20178841

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