To collect uniform and meaningful data on patients with Pompe disease who experience anaphylaxis, severe allergic reactions, and/or signals of severe cutaneous and/or systemic immune complex-mediated reactions following treatment with alglucosidase alfa.
Study Type
OBSERVATIONAL
Enrollment
110
Alglucosidase alfa IV infusion of 20 mg/kg; qow
Investigational Site Number 840016
Phoenix, Arizona, United States
Investigational Site Number 840002
Durham, North Carolina, United States
number of patients experience anaphylaxis, severe allergic reactions and/or signals of severe cutaneous and/or systematic immune complex-mediated reactions
collect meaningful data on patients with these outcomes following treatment with alglucosidase alfa
Time frame: 4 Years
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Investigational Site Number 840004
Hershey, Pennsylvania, United States
Investigational Site Number 840014
Pittsburgh, Pennsylvania, United States
Investigational Site Number 840008
Salt Lake City, Utah, United States
Investigational Site Number 840001
Fairfax, Virginia, United States
Investigational Site Number 056001
Ghent, Belgium
Investigational Site Number 056002
Leuven, Belgium
Investigational Site Number 056003
Leuven, Belgium
Investigational Site Number 203001
Prague, Czechia
...and 8 more locations