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Gene Therapy Trial Report

Summary

Safety Study of Recombinant Adeno-Associated Virus Acid Alpha-Glucosidase to Treat Pompe Disease


NCTID NCT00976352 (View at clinicaltrials.gov)
Description
Development Status Inactive
Indication Glycogen Storage Disease Type 2 (Pompe Disease)
Disease Ontology Term DOID:2752
Compound Name AAV1-CMV-hGAA
Sponsor University of Florida
Funder Type Other
Recruitment Status
Completed
Enrollment Count 9 (ACTUAL)
Results Posted View Results

Therapy Information


Target Gene/Variant GAA
Therapy Type Gene transfer
Therapy Route In-vivo
Mechanism of Action Functional gene replacement
Route of Administration Intramuscular (diaphragm)
Drug Product Type Viral vector
Delivery System Viral transduction
Vector Type AAV2/1
Editor Type none
Dose 1 1E12 vg (n=3)
Dose 2 5E12 vg (n=6)

Study Record Dates


Current Stage Phase1, Phase2
Submit Date 2009-07-13
Completion Date 2015-12
Last Update 2018-09-14

Participation Criteria


Eligible Age 2 Years - 18 Years
Standard Ages Child, Adult
Sexes Eligible for Study ALL
Eligibility Criteria
Inclusion Criteria: * Male or female subjects 2-18 years of age. * Have a diagnosis of Pompe, as defined by protein assay, DNA sequence of the acid alpha-glucosidase gene and clinical symptoms of the disease. * Using assisted ventilation at baseline. Mechanical Ventilation is defined as any use of ventilation support, (including but not limited to BiPAP, CPAP), a minimum of 1 hours per day. * Willing to discontinue aspirin, aspirin-containing products and other drugs that may alter platelet function, 7 days prior to dosing, resuming 24 hours after the dose has been administered. Exclusion Criteria: The subject must not: * Have required acute, as distinguished from long-term, maintenance or chronic suppressive, oral or intravenous antibiotic therapy for a respiratory infection within 15 days prior to baseline screening. * Have required oral or systemic corticosteroids within the last 15 days prior to baseline screening. * Have a platelet count less than 75,000/ cu mm. * Have an INR greater than 1.3. * Serological evidence of hepatitis B, hepatitis C, or HIV positive. * Be currently or within the past 30 days participating in any other research protocol involving investigational agents or therapies. * Have received gene transfer agents within the past 6 months. * Have history of platelet dysfunction, evidence of abnormal platelet function at screening or history of recent use of drugs that may alter platelet function which the subject is unable/unwilling to discontinue for study agent administration. * Have any other concurrent condition which, in the opinion of the investigator, would make the subject unsuitable for the study.
View Inclusion and Exclusion Criteria at ClinicalTrials.gov

Locations


No.of Trial Sites 1
Locations United States

Regulatory Information


Has US IND True
FDA Designations
Recent Updates Sponsors of this trial redesigned the drug product by changing the capsid (AAV2/1 -> AAV2/9) and promoter (CMV->DES), and site of administration (diaphragm -> tibialis anterior), updated trial record is NCT02240407

Resources/Links