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A Gene Therapy Study of RP-A501 in Male Patients With Danon Disease

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Rocket Pharmaceuticals

Status and phase

Enrolling
Phase 2

Conditions

Danon Disease

Treatments

Genetic: RP-A501

Study type

Interventional

Funder types

Industry

Identifiers

NCT06092034
RP-A501-0123

Details and patient eligibility

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 (AAV9) containing the human lysosome-associated membrane protein 2 isoform B (LAMP2B) transgene, in male patients with Danon Disease.

Full description

The study is a single arm Phase 2 clinical trial to characterize the safety and efficacy of RP-A501, a recombinant adeno-associated serotype 9 (rAAV9 capsid containing the human lysosome-associated membrane protein 2 isoform B (LAMP2B) transgene) in male patients with Danon Disease.

Male subjects ≥8 years of age will receive a single intravenous infusion of RP-A501.

Enrollment

14 estimated patients

Sex

Male

Ages

8+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Key Inclusion Criteria:

  1. Documentation of a pathogenic or likely pathogenic variant of the LAMP2 gene.

  2. Male.

  3. Age ≥8 years.

  4. Evidence of left ventricular hypertrophy with preserved systolic function phenotype as defined by each of the following:

    1. Abnormal thickening of Left ventricular wall,
    2. Left ventricular ejection fraction (LVEF) ≥ 50%.
  5. New York Heart Association (NYHA) Class II to III.

  6. High sensitivity Troponin I (hsTnI) ≥20% above the upper limit of normal (ULN)

  7. Ability to comply with study procedures including investigational therapy and follow-up evaluations.

Key Exclusion Criteria:

  1. Anti-AAV9 neutralizing antibody titer >1:40.
  2. Severe heart failure or requirement for advanced therapies.
  3. History of intracardiac thrombosis or arterial thromboembolic events including stroke, transient ischemic attack (TIA), acute coronary syndrome, myocardial infarction or unstable angina.
  4. Prior cardiac or other organ (lung, liver, other) transplantation.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

14 participants in 1 patient group

RP-A501
Experimental group
Description:
One planned dose of RP-A501 in cohorts of subjects with a confirmed diagnosis of Danon Disease.
Treatment:
Genetic: RP-A501

Trial contacts and locations

6

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Central trial contact

Clinical Information

Data sourced from clinicaltrials.gov

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