Alglucosidase alfa
Alglucosidase alfa, sold under the brand name Myozyme among others, is an enzyme replacement therapy (ERT) orphan drug for treatment of Pompe disease (Glycogen storage disease type II), a rare lysosomal storage disorder (LSD).Chemically speaking, the drug is an analog of the enzyme that is deficient in patients affected by Pompe disease, alpha-glucosidase. It is the first drug available to treat this disease. It was approved for medical use in the United States in April 2006, as Myozyme and in May 2010, as Lumizyme.
ATC code A16ATC code A16AB07ATCvet code QA16AB07Alglucosidase AlfaAlpha-glucosidaseC4758H7262N1274O1369S35Extraordinary MeasuresGenzymeGlycogen storage disease type IIHenri TermeerInborn errors of metabolismJohn Crowley (biotech executive)List of National Taiwan University peopleList of drugs: AlLumizymeMyozymeSanofiVesivirusWilliam Canfield
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Alglucosidase alfa
Alglucosidase alfa, sold under the brand name Myozyme among others, is an enzyme replacement therapy (ERT) orphan drug for treatment of Pompe disease (Glycogen storage disease type II), a rare lysosomal storage disorder (LSD).Chemically speaking, the drug is an analog of the enzyme that is deficient in patients affected by Pompe disease, alpha-glucosidase. It is the first drug available to treat this disease. It was approved for medical use in the United States in April 2006, as Myozyme and in May 2010, as Lumizyme.
has abstract
Alglucosidase alfa (Myozyme) i ...... later was het tekort opgelost.
@nl
Alglucosidase alfa, sold under ...... and in May 2010, as Lumizyme.
@en
Alglukozydaza alfa – glikoprot ...... zastępczej w chorobie Pompego.
@pl
ألغلوكوزيداز ألفا (بالإنجليزية ...... ختزان الغلايكوجين النمط الثاني
@ar
アルグルコシダーゼ アルファは、ポンペ病に対し酵素補充療法を ...... として開発された。ポンペ病に治療効果がある初めての薬である。
@ja
阿糖苷酶α(Alglucosidase alfa),商品名美而赞(Myozyme),是目前罕见病庞贝病全球唯一的注射剂和特效药。
@zh
alternative name
Myozyme, Lumizyme, others
@en
CAS number
420794-05-0
DrugBank
FDA UNII code
DTI67O9503
KEGG
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Wikipage page ID
13,081,045
page length (characters) of wiki page
Wikipage revision ID
1,000,086,031
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ATC prefix
A16
@en
ATC suffix
AB07
@en
CAS number
ChemSpiderID
none
@en
DailyMedID
Alglucosidase_alfa
@en
DrugBank
DB01272
@en
IUPAC name
Human glucosidase, prepro-α-[199-arginine,223-histidine]
@en
KEGG
D03207
@en
legal AU
S4
@en
legal US
Rx-only
@en
licence EU
yes
@en
molecular weight round
routes of administration
tradename
Myozyme, Lumizyme, others
@en
UNII
DTI67O9503
@en
Verifiedfields
changed
@en
verifiedrevid
477,314,655
Watchedfields
changed
@en
wikiPageUsesTemplate
hypernym
comment
Alglucosidase alfa (Myozyme) i ...... eft de behandeling minder zin.
@nl
Alglucosidase alfa, sold under ...... and in May 2010, as Lumizyme.
@en
Alglukozydaza alfa – glikoprot ...... zastępczej w chorobie Pompego.
@pl
ألغلوكوزيداز ألفا (بالإنجليزية ...... ختزان الغلايكوجين النمط الثاني
@ar
アルグルコシダーゼ アルファは、ポンペ病に対し酵素補充療法を ...... として開発された。ポンペ病に治療効果がある初めての薬である。
@ja
阿糖苷酶α(Alglucosidase alfa),商品名美而赞(Myozyme),是目前罕见病庞贝病全球唯一的注射剂和特效药。
@zh
label
Alglucosidase alfa
@en
Alglucosidase alfa
@nl
Alglukozydaza alfa
@pl
ألغلوكوزيداز ألفا
@ar
アルグルコシダーゼ アルファ
@ja
阿糖苷酶α
@zh