Heart Failure Clinical Trial

Modulation of SERCA2a of Intra-myocytic Calcium Trafficking in Heart Failure With Reduced Ejection Fraction

Summary

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.

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Full Description

MUSIC-HFrEF1 is an interventional study of SRD-001, an adeno-associated virus serotype 1 (AAV1) vector expressing the transgene for sarco(endo)plasmic reticulum Ca2+ ATPase 2a isoform (SERCA2a), in anti-AAV1 neutralizing antibody (NAb) negative subjects with ischemic or non-ischemic cardiomyopathy and New York Heart Association (NYHA) class III/IV symptoms of heart failure with reduced ejection fraction (HFrEF).

The Phase 1 trial is an open-label, uncontrolled study investigating two doses of SRD-001 at 3E13 and 4.5E13 viral genomes (vg) in 3-4 participants at each dose level.

The Phase 2 trial is a randomized, double-blind, placebo-controlled trial with prospective assignment to a single dose of either SRD-001 or placebo in a 1:1 ratio and a total sample size of N=50.

View Eligibility Criteria

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

Study is for people with:

Heart Failure

Phase:

Phase 1

Estimated Enrollment:

57

Study ID:

NCT04703842

Recruitment Status:

Recruiting

Sponsor:

Sardocor Corp.

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There are 5 Locations for this study

See Locations Near You

San Diego Cardiac Center
San Diego California, 92123, United States More Info
Emma Burkhalter, RN
Contact
858-244-6890
[email protected]
Brian Jaski, MD
Principal Investigator
University of California, San Francisco
San Francisco California, 94143, United States More Info
Kaye Reambonanza
Contact
415-514-6147
[email protected]
Richard Cheng, MD
Principal Investigator
Washington University in Saint Louis
Saint Louis Missouri, 63110, United States More Info
Annie Dirks, RN, BSN
Contact
314-454-8711
[email protected]
Gregory Ewald, MD
Principal Investigator
University of Texas Southwestern Medical Center
Dallas Texas, 75390, United States More Info
Therese Villina, MPHI, BSN
Contact
214-645-7083
[email protected]
Justin Grodin, MD
Principal Investigator
University of Washington Medicine
Seattle Washington, 98195, United States More Info
Katherine Nassans
Contact
206-543-6850
[email protected]
Kenta Nakamura, MD
Principal Investigator

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Phase:

Phase 1

Estimated Enrollment:

57

Study ID:

NCT04703842

Recruitment Status:

Recruiting

Sponsor:


Sardocor Corp.

How clear is this clinincal trial information?

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