AAV1/SERCA2a
Biological3E13 viral genomes fixed dose
NCT Number: NCT06061549
The goal of this clinical trial is to test an experimental gene therapy in participants with heart failure with preserved ejection fraction, also known as diastolic heart failure. The main questions it aims to answer are:
* safety and tolerability of the gene therapy; and * whether the gene therapy helps the heart ventricles relax during filling. Participants will undergo a one-time infusion of the gene therapy in the cardiac catheterization laboratory and then be followed for safety and effects on left-sided filling pressures while exercising. The first year will have multiple in-person visits followed by 4 years of biannual phone calls.
Interested in participating?
Request Info50 year and older
All sexes
Interventional
Phase 1
Duke University, Durham, North Carolina, United States
Eligible participants will undergo a one-time antegrade epicardial coronary artery infusion of gene therapy delivered to the 3 major cardiac territories of the left ventricle of the heart (anterior, lateral, inferior/posterior) or bypass grafts unless contraindicated. Post-procedure, the subject will be monitored continuously for a minimum of 4 hours and then discharged to home that same day if medically appropriate. Participants will be followed for 52 weeks as part of the main trial. On Day 2 and Week 1, subjects will be contacted by phone for a general safety assessment, and if clinically indicated, an in-person evaluation and assessment will be performed as soon as possible. On Weeks 2, 4, 12, 24 and 52, subjects will undergo general safety assessments. Additionally, at Weeks 24 and 52, subjects will undergo outpatient core resting and exercise transthoracic echocardiography, right heart catheterization with hemodynamic monitoring and gas exchange measurements, 6-minute wall test, cardiac biomarker testing and completion the Kansas City Cardiomyopathy Questionnaire. Upon completion of the active observation period, participants will continue to be followed for 4 years with bi-annual, semi-structured telephone or in-person questionnaires that collect information on overall status and other comorbid conditions of interest in gene therapy trials.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
3E13 viral genomes fixed dose
Time frame: Week 24 and Week 52
PCWP assessed by right heart catheterization; change in mmHg from baseline
Time frame: Week 24 and Week 52
PCWP assessed by right heart catheterization; change in mmHg from baseline
Time frame: Week 24 and Week 52
VO2 assessed by bicycle exercise; change in mL/min from baseline
Time frame: Week 24 and Week 52
Assessed by transesophageal echocardiography (ultrasound) using 2 methods: LV global peak early diastolic strain rate (1/s) and LV tau
Time frame: Week 24 and Week 52
Laboratory measurement (picograms per mL) in blood; high levels indicate the heart is working too hard to pump blood; decrease over time would indicate an improvement in heart failure condition
Time frame: Week 24 and Week 52
Assessed by transesophageal echocardiography (ultrasound); change in mL/m2 from baseline
Time frame: Week 24 and Week 52
Assessed by transesophageal echocardiography (ultrasound); change in %from baseline
Time frame: Week 24 and Week 52
Assessed by transesophageal echocardiography (ultrasound); change in % from baseline
Time frame: Week 24 and Week 52
Distance walked in 6 minutes, measured in meters; the longer distance walked, the better medical condition
Time frame: Week 24 and Week 52
Self-rated shortness of breath score with scale from 0 to 10, ranging from none to very, very severe
Time frame: Week 24 and Week 52
Measures symptoms, physical and social limitations, and quality of life in patients with heart failure; 23-item self-administered questionnaire; score of 0 to 100; 0-24, very poor to poor; 25-49, poor to fair; 50 to 74, faire to good; and 75 to 100, good to excellent
Time frame: Week 24 and Week 52
Classification of heart failure based on severity of symptoms; 4 classes, I, II, III or IV where class I is having no symptoms doing ordinary physical activity; class II is having fatigue, shortness of breath, palpitations or angina with ordinary physical activity; class II is being comfortable only at rest; and class IV is having symptoms even at rest
Contact information is provided by the study sponsor or research team.
Sardocor Corp.
Industry
A Phase 1b, Pilot Trial Evaluating the Safety and Pharmacodynamic Effects of SRD-001 (AAV1-SERCA2a) in Subjects With Heart Failure With Preserved Ejection Fraction
Acronym: MUSIC-HFpEF
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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