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

Pompe disease is an inherited condition of acid alpha-glucosidase (GAA) deficiency resulting in lysosomal accumulation of glycogen in all tissues. Glycogen accumulation leads to muscle dysfunction and profound muscle weakness. A wide spectrum of disease is characteristic and the most severe patients have cardiorespiratory failure, often fatal in the first two years of life. Researchers have developed a way to introduce the normal GAA gene into muscle cells with the expectation that the GAA protein will be produced at levels sufficient to reduce glycogen accumulation. This study will evaluate the safety of the experimental gene transfer procedure in individuals with GAA deficiency. The study will also determine what dose may be required to achieve improvement in measures of respiratory function.

The goals of the current study are to evaluate an experimental gene transfer procedure in which normal copies of the GAA gene are inserted into cells. In this study, a modified virus, adeno-associated virus (AAV), has been engineered to carry a normal copy of the GAA gene, known as rAAV1-CMV-hGAA, which is used to place normal copies of the GAA gene into diaphragm muscle cells. The purpose of this study is to evaluate the safety of rAAV1-CMV-hGAA delivery into individuals with GAA deficiency (Pompe Disease).

Participants currently using enzyme replacement therapy will continue to receive their regular medical regimen during the 12 month duration of the study. Participants will first attend a screening study visit to confirm study eligibility. Participants will then attend a 3-5 day inpatient visit, during which they will receive a series of intradiaphragmatic injections consisting of the study agent (rAAV1-CMV-hGAA). Follow-up study visits will occur on Days 14 and 90, 180, 270 and 365. Participants will have yearly follow-up evaluations by either telephone or mail for a total of 15 years, or as required by the FDA and other regulatory agencies.

• Drug: rAAV1-CMV-GAA
  rAAV-CMV-GAA via intramuscular injection into the diaphragm. Dose selection for cohort 1: 1.0 x 10e12 vector genomes Cohort 1 will have a total of 3 participants enrolled.
  Other Names:

  • Gene transfer
  • Gene therapy
  • Pompe disease
  • Diaphragm
  • GAA
• Drug: Study agent administration
  Direct intramuscular injection of study agent to the diaphragm muscle using video assisted thorascopy. Dose selection for cohort 2 and 3: 5.0 x 10e12 vector genomes
  Other Names:

  • Gene transfer
  • Gene therapy
  • Pompe disease
  • Diaphragm
  • GAA

• Experimental: Gene Therapy: Cohort 1, rAAV1-CMV-GAA
  Gene Therapy: Cohort 1, rAAV1-CMV-GAA: Dose selection for cohort 1: 1.0 x 10e12 vector genomes. Cohort 1 will have a total of 3 participants dosed with the study agent.
  Intervention: Drug: rAAV1-CMV-GAA
• Experimental: Gene Therapy: Cohort 2,Study agent administration
  Gene Therapy: Cohort 2,Study agent administration: Dose selection for cohort 2: 5.0 x 10e12 vector genomes Cohort = 3 subjects
  Intervention: Drug: Study agent administration
• Experimental: Gene Therapy Cohort 3, Study agent administration
  Gene Therapy Cohort 3, Study agent administration: Dose selection for cohort 2: 5.0 x 10e12 vector genomes Cohort = 4 subjects
  Intervention: Drug: Study agent administration

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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.