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Clinical Trials/NCT04080050
NCT04080050
Active, Not Recruiting
N/A

A Long-term Follow-up Study to Evaluate the Safety and Efficacy of RGX-501

REGENXBIO Inc.6 sites in 3 countries8 target enrollmentSeptember 30, 2019

Overview

Phase
N/A
Intervention
Single intravenous (IV) dose of human Low Density Lipoprotein Receptor (LDLR) Gene Therapy
Conditions
Homozygous Familial Hypercholesterolemia (HoFH)
Sponsor
REGENXBIO Inc.
Enrollment
8
Locations
6
Primary Endpoint
Number of incidents of new and unexpected adverse events and serious adverse events.
Status
Active, Not Recruiting
Last Updated
3 years ago

Overview

Brief Summary

This long-term observational study is designed to follow subjects who, during another Clinical Study, received gene therapy treatment used to treat their Homozygous Familial Hypercholesterolemia (HoFH) disease. This study is intended to follow those subjects for up to 5 years since they received treatment to look for any long-term safety concerns. There is no investigational drug or therapy provided as part of this study.

Detailed Description

Homozygous Familial Hypercholesterolemia (HoFH) is a rare genetic metabolic disorder characterized by absent or severely reduced capacity to catabolize circulating LDL particles by the hepatic LDL receptor. As a consequence, HoFH subjects present abnormal total plasma cholesterol (LDL-C) levels, resulting in severe atherosclerosis often leading to early onset of cardiovascular disease. Early initiation of aggressive treatment for these patients is therefore essential. Unfortunately, despite existing therapies, treated LDL-C levels could remain well above acceptable levels. Thus, the functional replacement of the defective LDLR via AAV-based liver-directed gene therapy, RGX-501, may be a viable approach to treat this disease and improve response to current lipid-lowering treatments. This is a prospective, observational study to evaluate the long-term safety and efficacy after a single administration of RGX-501. Eligible participants are those who previously have enrolled in a clinical study and received a single intravenous infusion of RGX-501.

Registry
clinicaltrials.gov
Start Date
September 30, 2019
End Date
September 29, 2025
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • To be eligible to participate in this study, a participant must have previously received RGX-501 in a separate parent trial, and the participant or participant's legal guardian(s) is/(are) willing and able to provide written, signed informed consent after the nature of the study has been explained, prior to any research-related procedures.

Exclusion Criteria

  • Not provided

Arms & Interventions

RGX-501

Study participants who have received RGX-501 gene therapy in a separate parent trial

Intervention: Single intravenous (IV) dose of human Low Density Lipoprotein Receptor (LDLR) Gene Therapy

Outcomes

Primary Outcomes

Number of incidents of new and unexpected adverse events and serious adverse events.

Time Frame: Up to 5 years after receiving treatment with RGX-501

The number of times a new and unexpected adverse event and/or serious adverse event is reported.

Secondary Outcomes

  • Absolute total cholesterol, LDL-C, very low density lipoprotein cholesterol (VLDL-C), high density lipoprotein cholesterol (HDL-C), calculated non-HDL-C, triglycerides (TG), and lipoprotein a (Lp(a)) over the study duration(Up to 5 years after receiving treatment with RGX-501)
  • Usage of lipid-lowering therapies over time(Up to 5 years after receiving treatment with RGX-501)
  • The absolute LDL-C level in mg/dL by beta quantification(Year 3 after receiving treatment with RGX-501)

Study Sites (6)

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