CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 2 enrolled
Drug / intervention
Recombinant Adeno-Associated Virus Acid Alpha-Glucosidase +7 moregenetic
Likely dose
Rapamycin 2 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02240407
NCT02240407Phase 1Completed

Evaluation of Re-administration of Recombinant Adeno-Associated Virus Acid Alpha-Glucosidase (rAAV9-DES-hGAA) in Patients With Late-Onset Pompe Disease (LOPD)

University of Florida·interventional·Posted Sep 15, 2014·Updated Apr 5, 2022

In Brief

A Phase 1 clinical trial evaluating Recombinant Adeno-Associated Virus Acid Alpha-Glucosidase, Rapamycin, and 6 other interventions for Pompe Disease. Completed, enrolled 2 participants across 1 site.

Detailed Summary

A recombinant AAV vector has been generated to carry the codon-optimized acid alpha-glucosidase (coGAA) gene expressed from a human desmin enhancer/promoter (DES). The proposed clinical trial is a within-participant, double-blind, randomized, phase I controlled study evaluating the toxicology, biodistribution and potential activity of re-administration of rAAV9-DES-hGAA injected intramuscularly into the TA. Nine participants (18 to 50-years old) who reside within the United States with Late-Onset Pompe Disease (LOPD) will be included. The goal of the immune modulation strategy is to ablate B-cells (Rituximab and Sirolimus) prior to the initial exposure to the study agent in one leg and the subsequent exposure of the same vector to the contralateral leg after four months. At each study agent dosing, the contralateral leg will receive excipient. Patients will act as their own controls. Repeated measures, at baseline and during the following 3 months after each injection, will assess the safety, biochemical and functional impact of the vector.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPompe Disease
CountriesUnited States

Timeline

Phase 1CompletedFinished
201520162017201820192020202120222023202420252026
First PostedSep 15, 2014
Enrollment StartOct 17, 2017
Primary CompletionAug 26, 2021
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 11.8 years ago

Interventions

Recombinant Adeno-Associated Virus Acid Alpha-Glucosidasegenetic

The dose selected for this study is a fixed dose of 4.6 x 10\^13 vg per TA muscle (range of 7.64 x 10\^11 vg/gm to 4.6 x 10\^11 vg/gm based on TA weight).

Rapamycindrug

Patients will receive Rapamycin (dose 0.6-2 mg/m\^2/day, adjusted to maintain a trough serum sirolimus level of 2-4 ng/mL.) every day starting from 7 days before first injection of AAV9 until four months after second injection.

salineother

Same volume as rAAV9-DES-hGAA injection will be used.

Rituxandrug

Patients will receive Rituxan (dose: 750 mg/m\^2 twice) 21 and 7 day prior first AAV9 injection, with a Rituxan dose 375 mg/m\^2 on the day of the injection. Rituxan will be repeated 7 days prior to the 2nd injection of the vector. The maintenance dose of Rituxan will be 375 mg/m\^2.

Diphenhydraminedrug

25-50mg will be provided before each Rituximab dose.

Acetaminophendrug

We will provide 650 mg of tylenol before each dose of Rituximab.

Lidocainedrug

Lidocaine will be used based on standard of care: Percutaneous infiltration, concentration 0.5-1%, 1-10 mL, 5-300mg total dose.

LMX 4 Topical Creamdrug

Topical anesthesia cream will be used prior to gene therapy/saline injection.