SRD-001
BiologicalAAV1/SERCA2a
NCT Number: NCT04703842
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.
Interested in participating?
Request Info18 year–80 year
All sexes
Interventional
Phase 1 / Phase 2
San Diego Cardiac Center, San Diego, California, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Main Inclusion Criteria:
Main Exclusion Criteria:
AAV1/SERCA2a
SRD-001 matching placebo
Time frame: Baseline to Month 6 and Month 12
New York Heart Association classification (I, II, III or IV)
Time frame: Baseline to Month 6 and Month 12
Quality of life as assessed by Kansas City Cardiomyopathy Questionnaire: 0-24, very poor to poor; 25-49, poor to fair; 50-74, fair to good; and 75-100, good to excellent
Time frame: Baseline to Month 6 and Month 12
Distance walked during the 6MWT
Time frame: Baseline to Month 6 and Month 12
Left ventricular end systolic volume (LVESV) as assessed by echocardiography
Time frame: Baseline to Month 6 and Month 12
HF-related hospitalization, ambulatory worsening heart failure, all-cause death, MCSD and transplant
Time frame: 6 and 12 months
Treatment-emergent adverse events
Time frame: 12 months
Those who complete the trial vs withdraw consent, are lost to follow-up, or withdrawn due to an AE or other reason
Time frame: 6 and 12 months
Changes in heart failure related medications
Time frame: Baseline to Month 6 and Month 12
Hematologic, serum chemistries, NT-proBNP and troponin
Time frame: Baseline to Month 6 and Month 12
New arrhythmias
Time frame: Baseline to Month 6 and Month 12
Change from baseline in physical examination findings
Time frame: Baseline to Month 6 and Month 12
New arrhythmias
Contact information is provided by the study sponsor or research team.
Sardocor Corp.
Industry
A Phase 1/2 Trial of the Safety and Efficacy of SRD-001 (AAV1/SERCA2a) in Subjects With Heart Failure With Reduced Ejection Fraction
Acronym: MUSIC-HFrEF1
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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