Treating Heart Failure With hiPSC-CMs

Heart Failure Clinical Trial

Official title:

Epicardial Injection of Human Pluripotent Stem Cell-derived Cardiomyocytes to Treat Severe Chronic Heart Failure

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05223894
• Other study ID #: ZMLiu
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: June 30, 2022
• Est. completion date: December 30, 2025

Study information

• Verified date: November 2023
• Source: Help Therapeutics
• Contact: Gang Yang, MD,PhD
• Phone: +86-18601406982
• Email: yanggang[@]helpsci.com.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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 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 and efficacy of intramyocardial delivery of cardiomyocytes at the time of coronary artery bypass grafting in patients with chronic heart failure.

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, 3, 6 and 12 months after cell transplantation for safety and efficacy.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 20
• Est. completion date: December 30, 2025
• Est. primary completion date: December 30, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 35 Years to 75 Years

Eligibility

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 = 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).

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 TNF-a 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.

Related Conditions & MeSH terms

• Heart Failure

Intervention

Biological:
• hiPSC-CM therapy
Injection of allogenic human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) during coronary artery bypass grafting surgery. 100 million hPSC-CMs in 2.5-5 mL medium suspension will be injected into the myocardium.

Other:
• Control
Coronary artery bypass grafting surgery only.

Locations

Country	Name	City	State
China	Shanghai east Hospital	Shanghai	Shanghai

Sponsors (2)

Lead Sponsor	Collaborator
Help Therapeutics	Shanghai East Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of serious adverse events(SAEs) within 1 month post-CABG surgery.	Incidence of serious adverse events(SAEs) within 1 month post-CABG surgery. These include death, fatal myocardial infarction, stroke, cardiac tamponade, cardiac perforation, hemodynamic ventricular arrhythmias (duration > 15s), and new allogeneic human neoplasms.	1 Month Post-operation
Secondary	Size of infracted myocardium assessed by MRI	Size of infracted myocardium;	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Left Ventricular systolic performance as assessed by MRI	left ventricular side wall thickness at diastolic; interventricular septum thickness;	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Left ventricular ejection fraction assessed by MRI	left ventricular ejection fraction;	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Overall Left Ventricular systolic performance as assessed by MRI	left ventricular end-systolic volume and end-diastolic volume; stroke volume;	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Cardiac output assessed by MRI	cardiac output;	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Myocardium density assessed by MRI	myocardium density;	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Left ventricular mass assessed by MRI	left ventricular mass at diastolic;	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Overall Left Ventricular systolic performance as assessed by Echocardiogram	Interventricular septum thickness at diastolic; left ventricular posterior wall thickness at diastolic;	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Left Ventricular systolic performance as assessed by Echocardiogram	left ventricular end-systolic diameter and end-diastolic diameter; left atrial diameter;	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Left ventricular ejection fraction assessed by Echocardiogram	left ventricular ejection fraction;	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Mitral flow pattern (E/A) assessed by Echocardiogram	mitral flow pattern (E/A) ;	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Overall Left Ventricular systolic performance as assessed by PET/ECT Scan	Myocardium perfusion	Baseline, 6 and 12 Months Post-operation
Secondary	Functional status by 6 minute walk test	Evaluate Functional Capacity via the Six Minute Walk Test	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Functional status by New York Heart Association (NYHA) Classification	Evaluate Functional Capacity via New York Heart Association (NYHA) Class Determination.; It classifies patients in one of four categories based on their limitations during physical activity; Class I - No symptoms and no limitation in ordinary physical activity, e.g. shortness of breath when walking, climbing stairs etc.; Class II - Mild symptoms (mild shortness of breath and/or angina) and slight limitation during ordinary activity.; Class III - Marked limitation in activity due to symptoms, even during less-than-ordinary activity, e.g. walking short distances (20-100 m).Comfortable only at rest.; Class IV - Severe limitations. Experiences symptoms even while at rest. Mostly bedbound patients.	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Minnesota Living With Heart Failure Questionnaire (MLHFQ)	Evaluate Quality Of Life Changes via Minnesota Living with Heart Failure (MLHF). The Maximum possible scores being 105 and the minimum 0. Higher scores indicate a worse or worsening quality of life, while lower scores or decreasing scores indicate a better quality of life.	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Incidence of Serious Adverse Events (SAE)	SAE justified (all undesirable or unintended diseases or laboratory and imaging disorders and symptoms that occur in subjects after CABG surgery and 12 months postoperative follow-up, or until the subject withdrawals from the study. AE grading will be based on Common Terminology Criteria for Adverse Events (CTCAE) V5.0.)	Baseline, 1~12Months Post-operation
Secondary	Incidence of severe arrhythmia	Clinically significant arrhythmias will be recorded by Electrocardiogram monitoring	First month post-operatively
Secondary	Changes in penal reactive antibodies (PRA)	Changes in penal reactive antibodies (PRA) as assessed via blooddraw	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Changes in donor specific antibodies (DSA)	Changes in donor specific antibodies (DSA) as assessed via blooddraw	Baseline, 1, 3, 6 and 12 Months Post-operation
Secondary	Changes in cytokines	Change in NT-proBNP as assessed via blooddraw	Baseline,1, 3, 6 and 12 Months Post-operation