The purpose of this study is to evaluate the safety, tolerability, and efficacy of a single intravenous infusion of SPK-3006 in adults with clinically moderate, late-onset Pompe disease receiving enzyme replacement therapy (ERT). Participants will be treated in sequential, dose-level cohorts.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Number of adverse and serious adverse events (AEs/SAEs), including clinically significant abnormal laboratory values.
Timeframe: Up to 5 years
Occurrence of immune response against AAV capsid
Timeframe: Up to 5 years
Occurrence of immune response against GAA transgene
Timeframe: Up to 5 years