Clinical trial

A Phase 1/2 Trial of the Safety and Efficacy of SRD-001 (AAV1/SERCA2a) in Subjects With Heart Failure With Reduced Ejection Fraction

Name
SRD-001-1001
Description
It is believed that targeted SERCA2a enzyme replacement in HFrEF patients will correct defective intracellular Ca2+ hemostasis, resulting in improved cardiac contractile function and energetics which will, in turn, translate to improved clinical outcomes. Additionally, it is hypothesized that correcting SERCA2a dysfunction will also improve coronary blood flow through correction of the impaired endothelium-dependent nitric oxide-mediated vasodilatation observed in heart failure.
Trial arms
Trial start
2021-09-23
Estimated PCD
2025-12-31
Trial end
2028-12-01
Status
Recruiting
Phase
Early phase I
Treatment
SRD-001
AAV1/SERCA2a
Arms:
SRD-001
Placebo
SRD-001 matching placebo
Arms:
Placebo
Size
57
Primary endpoint
Change from baseline in symptomatic parameters
Baseline to Month 6 and Month 12
Change from baseline in symptomatic parameters
Baseline to Month 6 and Month 12
Change from baseline in physical parameter
Baseline to Month 6 and Month 12
Change from baseline in LV function/remodeling
Baseline to Month 6 and Month 12
Rate of recurrent events
Baseline to Month 6 and Month 12
Rate of adverse events
6 and 12 months
Eligibility criteria
Main Inclusion Criteria: * Chronic ischemic or non-ischemic cardiomyopathy * NYHA class III/IV * LVEF ≤35% * Guideline-directed medical therapy for heart failure; ICD Main Exclusion Criteria: * Restrictive cardiomyopathy, hypertrophic cardiomyopathy, acute myocarditis, pericardial disease, amyloidosis, infiltrative cardiomyopathy, uncorrected thyroid disease or discrete left ventricular (LV) aneurysm * Prior heart transplantation, left ventricular reduction surgery (LVRS), cardiomyoplasty, passive restraint device (e.g., CorCap™ Cardiac Support Device), mechanical circulatory support device (MCSD) or cardiac shunt * Likely to receive cardiac resynchronization therapy, cardiomyoplasty, LVRS, conventional revascularization procedure or valvular repair in the 6 months following treatment * Likely need for an immediate heart transplant or MCSD implant due to hemodynamic instability * Inadequate hepatic and renal function * Diagnosis of, or treatment for, any cancer within the last 5 years except for basal cell carcinoma or carcinomas in situ where surgical excision was considered curative
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1', 'PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 57, 'type': 'ESTIMATED'}}
Updated at
2024-03-26

1 organization

2 products

4 indications

Organization
Sardocor
Product
SRD-001
Indication
Heart Failure
Indication
systolic
Product
Placebo