A Gene Therapy Study of RP-A501 in Male Patients With Danon Disease
Rocket Pharmaceuticals Inc. · NCT06092034
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 8+ · Men only
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 2
- Target enrollment
- 18
- US sites recruiting
- 3
- Study start
- September 5, 2023
- Record last updated
- October 6, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This is a single arm Phase 2 trial to evaluate the efficacy and safety of RP-A501, a recombinant adeno-associated virus serotype 9 (rAAV9) vector containing the human lysosome-associated membrane protein 2 isoform B (LAMP2B) transgene, in male patients with Danon disease.
Being studied: RP-A501
Conditions: Danon Disease
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Key Inclusion Criteria
- Documentation of a pathogenic or likely pathogenic variant of the LAMP2 gene.
- Male.
- Age ≥8 years.
- Evidence of left ventricular hypertrophy with preserved systolic function phenotype as defined by each of the following:
- Abnormal thickening of left ventricular wall,
- Left ventricular ejection fraction (LVEF) ≥ 50%.
- New York Heart Association (NYHA) Class II to III.
- High sensitivity Troponin I (hsTnI) ≥20% above the upper limit of normal (ULN) ≤ 12 months prior to screening.
- Ability to comply with study procedures including investigational therapy and follow-up evaluations.
Key Exclusion Criteria
- Anti-AAV9 neutralizing antibody titer >1:40.
- Severe heart failure or requirement for advanced therapies (requirement for intravenous inotropic, vasodilator, or diuretic therapy within the 30 days prior to enrollment, presence or requirement for mechanical circulatory support (MCS), and presence or requirement for mechanical ventilation).
- History of intracardiac thrombosis or arterial thromboembolic events including stroke, transient ischemic attack (TIA), acute coronary syndrome, myocardial infarction or unstable angina.
- Prior cardiac or other organ (lung, liver, other) transplantation.
Recruiting US locations
University of California, San Diego
La Jolla, CA 92037
Site contact: Barry Greenberg, MD · 858-246-2987 · Bgreenberg@health.ucsd.edu
Boston Children's Hospital
Boston, MA 02115
Site contact: Emily Morris · Emily.Morris@childrens.harvard.edu
Children's Hospital of Philadelphia
Philadelphia, PA 19104
Site contact: Joseph Rossano, MD · rossanoj@chop.edu
Study contacts (from the official record)
- Clinical Information · 646-627-0033 · clinicaltrials@rocketpharma.com
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