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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
4
adeno-associated viral (AAV) vector
Barrow Neurological Institute
Phoenix, Arizona, United States
University of California Irvine Health
Orange, California, United States
Emory University School of Medicine
Atlanta, Georgia, United States
University of Kansas Medical Center Research Institute
Kansas City, Kansas, United States
University of Minnesota
Minneapolis, Minnesota, United States
Number of adverse and serious adverse events (AEs/SAEs), including clinically significant abnormal laboratory values.
Adverse events.
Time frame: Up to 5 years
Occurrence of immune response against AAV capsid
Time frame: Up to 5 years
Occurrence of immune response against GAA transgene
Time frame: Up to 5 years
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Oregon Health & Science University
Portland, Oregon, United States
University of Pennsylvania
Philadelphia, Pennsylvania, United States
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, United States
University of Utah
Salt Lake City, Utah, United States
Lysosomal and Rare Disorders Research & Treatment Center
Fairfax, Virginia, United States
...and 19 more locations