Status:

UNKNOWN

Treating Heart Failure With hiPSC-CMs

Lead Sponsor:

Help Therapeutics

Collaborating Sponsors:

Shanghai East Hospital

Conditions:

Heart Failure

Eligibility:

All Genders

35-75 years

Phase:

PHASE1

PHASE2

Brief Summary

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 ...

Detailed 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 a...

Eligibility Criteria

Inclusion

  • Aged 35-75 (including 35 and 75).
  • Have signed the Informed Consent Form (ICF).
  • Patients have chronic left ventricular dysfunction.
  • Patients have NYHA Class III-IV cardiac function even after improved medication for the treatment of advanced chronic heart failure.
  • Patients have indications for Coronary Artery Bypass Grafting.
  • 20% ≤ LVEF ≤ 40% as determined by echocardiogram (data collected up to 3 months prior to inclusion evaluation are valid; data collected within 1 month since a myocardial infarction are invalid).
  • Weakening or absence of segmental regional wall motion as determined by standard imaging.

Exclusion

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

Key Trial Info

Start Date :

June 30 2022

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 30 2025

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT05223894

Start Date

June 30 2022

End Date

December 30 2025

Last Update

November 22 2023

Active Locations (1)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

Shanghai east Hospital

Shanghai, Shanghai Municipality, China