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Treating Heart Failure With hPSC-CMs (HEAL-CHF)

H

Help Therapeutics

Status and phase

Completed
Phase 2
Phase 1

Conditions

Heart Failure

Treatments

Biological: hPSC-CM Therapy

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

Heart failure has a high morbidity and mortality because the heart is one of the least regenerative organs in the human body. Drug treatments for heart failure manage symptoms but do not restore lost myocytes. Cellular replacement therapy is a potential approach to repair damaged myocardial tissue, restore cardiac function, which has become a new strategy for the treatment of heart failure. The purpose of this study is to assess the safety, feasibility and efficacy of intramyocardial delivery of cardiomyocytes at the time of coronary artery bypass grafting in patients with chronic heart failure.

Full description

Patients with heart failure will be treated with allogenic human pluripotent stem cell-derived cardiomyocytes ( hPSC-CM ) from healthy donors. The cells will be injected directly into the myocardium at time of coronary artery bypass grafting. Patients will be assessed at 1, 6 and 12 months after cell transplantation for safety, feasibility and efficacy.

Enrollment

20 patients

Sex

All

Ages

35 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

  1. Aged 35-75 (including 35 and 75).
  2. Have signed the Informed Consent Form (ICF).
  3. Patients have chronic left ventricular dysfunction.
  4. Patients have NYHA Class III-IV cardiac function even after improved medication for the treatment of advanced chronic heart failure.
  5. Patients have indications for Coronary Artery Bypass Grafting.
  6. 20% ≤ LVEF ≤ 45% as determined by echocardiogram (data collected up to 6 months prior to inclusion evaluation are valid; data collected within 1 month since a myocardial infarction are invalid).
  7. Weakening or absence of segmental regional wall motion as determined by standard imaging.

Exclusion criteria

  1. PRA ≥ 20% or DSA-positive.
  2. Patient received ICD transplantation, CRT or similar treatment.
  3. Patients with valvular heart disease or received heart valvular disease
  4. Patients received treatment of percutaneous transluminal coronary intervention (PCI)
  5. Patients with atrial fibrillation
  6. Patients previously suffered sustained ventricular tachycardia or sudden cardiac death.
  7. Baseline glomerular filtration rate <30ml/min/1.73m2.
  8. Liver dysfunction, as evidenced by enzymes (AST and ALT) greater than three times the ULN.
  9. Hematological abnormality: A hematocrit <25% as determined by HCT, white blood cell<2500/ul or platelet values <100000/ul without another explanation.
  10. Known, serious radiographic contrast allergy, penicillin allergy, streptomycin allergy.
  11. Coagulopathy (INR>1.3) not due to a reversible cause.
  12. Contra-indication to performance of a MRI scan.
  13. Recipients of organ transplant.
  14. Clinical history of malignancy within 5 years (patients with prior malignancy must be disease free for 5 years).
  15. Non-cardiac condition that limits lifespan <1 year.
  16. On chronic therapy with immunosuppressant medication, such as glucocorticoid and TNFα antagonist.
  17. Patients allergy to or cannot use immunosuppressant.
  18. Serum positive for HIV, HBV, HCV, TP.
  19. Currently enrolled other investigational therapeutic or device study.
  20. Patients who are pregnant or breast feeding.
  21. Other conditions that researchers consider not suitable to participate in this study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

20 participants in 2 patient groups

hPSC-CM Therapy
Experimental group
Description:
Procedure: Injection of allogenic human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) during coronary artery bypass grafting surgery. 200 million hPSC-CMs in 2.5-5 mL medium suspension will be injected into the myocardium.
Treatment:
Biological: hPSC-CM Therapy
Control
Sham Comparator group
Description:
Procedure: Coronary artery bypass grafting surgery only.
Treatment:
Biological: hPSC-CM Therapy

Trial contacts and locations

1

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Central trial contact

Jiaxian Wang, MD, PhD

Data sourced from clinicaltrials.gov

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