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Gene Therapy Trial Browser
Clinical Trial Report
Gene Therapy Trial Report
Summary
A Phase 1, Dose Escalation Trial of RP-A601 in Subjects With PKP2 Variant-Mediated Arrhythmogenic Cardiomyopathy (PKP2-ACM)
NCTID
NCT05885412
(View at clinicaltrials.gov)
Description
This Phase 1 dose escalation trial will assess the safety and preliminary efficacy of a single dose intravenous infusion of RP-A601 in high-risk adult patients with PKP2-ACM.
(Show More)
Development Status
Active
Indication
PKP2 Arrhythmogenic Cardiomyopathy (PKP2-ACM)
Disease Ontology Term
DOID:0050431
Compound Name
RP-A601
Compound Description
AAVrh.74-PKP2a
Sponsor
Rocket Pharmaceuticals Inc.
Funder Type
Industry
Recruitment Status
Recruiting
Enrollment Count
9
Results Posted
Not Available
Therapy Information
Target Gene/Variant
PKP2
Therapy Type
Gene transfer
Therapy Route
In-vivo
Mechanism of Action
Functional gene replacement
Route of Administration
Intravenous
Drug Product Type
Viral vector
Target Tissue/Cell
Delivery System
Viral transduction
Vector Type
AAVrh.74
Editor Type
none
Dose 1
Starting dose: 8E13 GC/kg
Dose 2
Dose 3
Dose 4
Dose 5
Study Record Dates
Current Stage
Phase1
Submit Date
2023-05-22
Completion Date
2026-09
Last Update
2024-10-04
Participation Criteria
Eligible Age
>=18 Years
Standard Ages
Adult, Older adult
Sexes Eligible for Study
ALL
Locations
No.of Trial Sites
3
Locations
United States
Regulatory Information
Has US IND
True
FDA Designations
Fast Track, Orphan Drug Designation
Recent Updates
Preliminary data from the Phase 1 study is expected in the first half of 2025
Resources/Links
News and Press Releases
(Corporate Presentation) November 2024
Rocket Pharmaceuticals Receives Orphan Medicinal Product Designation from the European Commission for RP-A601 for PKP2 Arrhythmogenic Cardiomyopathy
Preclinical Publications
AAV-Mediated Delivery of Plakophilin-2a Arrests Progression of Arrhythmogenic Right Ventricular Cardiomyopathy in Murine Hearts: Preclinical Evidence Supporting Gene Therapy in Humans