Search

Displaying all 4 results
DrugBest match

Alglucosidase alfa

go.drugbank.com/drugs/DB01272
ApprovedInvestigational

Aglucosidase alfa consists of the human enzyme acid alpha-glucosidase (GAA) which is essential for the degradation of glygogen to glucose in lysosomes. It is encoded by the most predominant of nine observed haplotypes of this gene. Aglucosidase alfa is produced by recombinant DNA technology in a Chinese hamster ovar...

  1. Drug

    Avalglucosidase alfa

    go.drugbank.com/drugs/DB16099
    ApprovedInvestigational

    First developed by Sanofi Genzyme, avalglucosidase alfa is a chemically modified version of [alglucosidase alfa], where synthetic bis-phosphorylated oligosaccharides were attached to the structure to improve … [A232955] Avalglucosidase alfa is a recombinant form of GAA that restores deficient enzyme levels.

    Synonyms: avalglucosidasa alfa, Avalglucosidase alfaCategories: avalglucosidase alfa
  2. Drug

    Cipaglucosidase alfa

    go.drugbank.com/drugs/DB16708
    ApprovedInvestigational

    Compared to alglucosidase alfa, cipaglucosidase alfa has a higher M6P content. … [A232955] Other types of enzyme replacement therapy for the treatment of Pompe disease include [alglucosidase alfa] and [avalglucosidase alfa].

    Categories: cipaglucosidase alfaSynonyms: Cipaglucosidase alfa
  3. Indication

    Glycogen Storage Disease Type II

    go.drugbank.com/conditions/DBCOND0002595
    Drugs: Alglucosidase alfa · Avalglucosidase alfa