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RECRUITING
NCT06092034
PHASE2

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

Sponsor: Rocket Pharmaceuticals Inc.

View on ClinicalTrials.gov

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

GENETIC

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