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NCT Number: NCT04703842

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

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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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

San Diego Cardiac Center, San Diego, California, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

SRD-001

Biological

AAV1/SERCA2a

Placebo

Drug

SRD-001 matching placebo

Primary outcomes

  1. Change from baseline in symptomatic parameters

    Time frame: Baseline to Month 6 and Month 12

    New York Heart Association classification (I, II, III or IV)

  2. Change from baseline in symptomatic parameters

    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

  3. Change from baseline in physical parameter

    Time frame: Baseline to Month 6 and Month 12

    Distance walked during the 6MWT

  4. Change from baseline in LV function/remodeling

    Time frame: Baseline to Month 6 and Month 12

    Left ventricular end systolic volume (LVESV) as assessed by echocardiography

  5. Rate of recurrent events

    Time frame: Baseline to Month 6 and Month 12

    HF-related hospitalization, ambulatory worsening heart failure, all-cause death, MCSD and transplant

  6. Rate of adverse events

    Time frame: 6 and 12 months

    Treatment-emergent adverse events

Secondary outcomes

  1. Proportion of subjects who complete the trial

    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

  2. Concomitant medication use

    Time frame: 6 and 12 months

    Changes in heart failure related medications

  3. Incidence of abnormal laboratory test results

    Time frame: Baseline to Month 6 and Month 12

    Hematologic, serum chemistries, NT-proBNP and troponin

  4. Incidence of abnormal ECG results

    Time frame: Baseline to Month 6 and Month 12

    New arrhythmias

  5. Incidence of abnormal physical examination findings

    Time frame: Baseline to Month 6 and Month 12

    Change from baseline in physical examination findings

  6. Incidence of abnormal findings from interrogation of implantable cardioverter defibrillator

    Time frame: Baseline to Month 6 and Month 12

    New arrhythmias

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Sardocor Corp.

Industry

Registry information

Official study title

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

Important dates

Study start
2021
Primary completion
2025
Study completion
2028
First posted
Jan 11, 2021
Registry last updated
Mar 26, 2024

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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