This is the first in human treatment with ST-920, an adeno-associated virus (AAV2/6) vector encoding the complementary deoxyribonucleic acid (cDNA) for human a-Gal A. The purpose of this study is to evaluate the safety and tolerability of ascending doses of ST-920. ST-920 aims to provide stable, long-term production of α-Gal A at therapeutic levels in subjects with Fabry disease. The constant production of α-Gal A in humans should, importantly, enable reduction and potentially clearance of Fabry disease substrates Gb3 and lyso-Gb3. On Day 1, patients will be infused intravenously with a single dose of ST-920 and followed for a period of 52 weeks.
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Incidence of Treatment-emergent Adverse Events (TEAEs) - All
Timeframe: Up to 12 months after the ST-920 infusion
Incidence of Treatment-emergent Adverse Events (TEAEs) - Related to ST-920
Timeframe: Up to 12 months post ST-920 infusion
Incidence of Treatment-emergent Adverse Events (TEAEs) - Serious
Timeframe: Up to 12 month post ST-920 infusion
Incidence of Treatment-emergent Adverse Events (TEAEs) - Any TEAEs Leading to Study Discontinuation or Withdrawal
Timeframe: Up to 12 month post ST-920 infusion