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A Gene Therapy Study of RP-A501 in Male Patients With Danon Disease
Sponsor: Rocket Pharmaceuticals Inc.
Summary
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.
Official title: Gene Therapy for Danon Disease: A Phase 2 Study Evaluating the Efficacy and Safety of Intravenously Administered Adeno-Associated Virus Serotype 9 (rAAV9) Vector Containing the Human LAMP2 Isoform B Transgene (RP-A501; AAV9.LAMP2B) in Male Patients With Danon Disease
Key Details
Gender
MALE
Age Range
8 Years - Any
Study Type
INTERVENTIONAL
Enrollment
18
Start Date
2023-09-05
Completion Date
2032-06
Last Updated
2026-10-06
Healthy Volunteers
No
Conditions
Interventions
RP-A501
RP-A501 is a gene therapy product consisting of an rAAV9 capsid containing the human LAMP2B transgene which will be administered as a single IV infusion. Dose of RP-A501: Cohorts 1, 2 \& 3 = 6.7 x10\^13 genome copies (GC)/kg; Cohort 4 = 3.8 x10\^13 GC/kg. An immunomodulation regimen is initiated before RP-A501 administration to reduce the risk of gene therapy-related complications. The regimen includes rituximab or a biosimilar, administered in two doses for Cohorts 1-3 and three doses for Cohort 4, along with sirolimus and corticosteroids. Pegcetacoplan was incorporated into the immunomodulation regimen for Cohort 3 but excluded in Cohort 4.
Locations (6)
University of California, San Diego
La Jolla, California, United States
Boston Children's Hospital
Boston, Massachusetts, United States
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
German Heart Center Munich
Munich, Germany
Meyer Children's Hospital
Florence, Italy
Great Ormond Street Hospital & UCL Institute of Cardiovascular Science
London, United Kingdom