Clinical data | |
---|---|
Trade names | Pombiliti |
Other names | ATB-200, ATB200, cipaglucosidase alfa-atga |
Routes of administration | Intravenous |
Drug class | Enzyme replacement |
ATC code |
|
Legal status | |
Legal status |
|
Identifiers | |
CAS Number |
|
DrugBank |
|
UNII |
|
KEGG |
|
ChEMBL |
|
Chemical and physical data | |
Formula | C4489H6817N1197O1298S32 |
Molar mass | 99347.92 g·mol−1 |
Cipaglucosidase alfa, sold under the brand name Pombiliti, and used in combination with miglustat, is a medication used for the treatment of glycogen storage disease type II (Pompe disease).[3] Cipaglucosidase alfa is a recombinant human acid α-glucosidase enzyme replacement therapy that provides an exogenous source of acid α-glucosidase.[3]
The most common side effects include chills, dizziness, flushing, sleepiness, chest discomfort, cough, swelling at the infusion site and pain.[3]
Cipaglucosidase alfa was approved for medical use in the European Union in March 2023.[3]
Pombiliti EPAR
was invoked but never defined (see the help page).