This is a study of gene therapy to treat alpha 1-antitrypsin (AAT) deficiency. This study aims to treat AAT deficiency with a single administration of AAV8hAAT(AVL), a gene therapy that codes for an oxidation resistant form of the AAT protein, which if safe and if efficacious, will protect the lung on a persistent basis. We hope to learn the safety/toxicity and initial evidence of efficacy of intravenous delivery of this gene therapy to alpha 1-antitrypsin deficient individuals.
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Safety of AAV8hAAT(AVL), as measured by number of subjects with at least 1 serious adverse event.
Timeframe: Approximately 1 year
Toxicity of AAV8AAT(AVL), as measure by number of subjects with any dose limiting toxicity
Timeframe: Approximately 2 years
Establishing a maximum tolerable dose of AAV8hAAT(AVL)
Timeframe: Approximately 2 years