alpha-galactosidase

(redirected from Agalsidase alfa)

alpha-galactosidase

an enzyme that catalyzes the conversion of alpha-d-galactoside to d-galactose.
References in periodicals archive ?
Also included are drug profiles for (migalastat hydrochloride + agalsidase alfa), agalsidase alfa, agalsidase beta biosimilar, Alpha-Galactosidase, Genz-682452, GZ-402671, JR-051, migalastat hydrochloride, Next Generation biologics for Pompe, Fabry and Hunter, NP-003, PRX-102 and Recombinant Enzyme to Replace Alpha-Galactosidase A for Fabry's Disease.
Framework Agreement contract dossier dle centralized supply of drugs Cytarabine (DOE), Docetaxel (DOE), Adefovir (DOE), Liposomal Amphotericin B, velaglucerase (DOE), Anti Inhibitor Coagulant Complex, agalsidase alfa (DOE), cabazitaxel (DOE ), Abiraterone (DOE), Parental Levetirazepam (DOE), Cetuximab (DOE), Tenofovier (DOE), Clofarabine (DOE), alglucosidase alfa (DOE), Rasburicase (DOE) and Everolimus (DOE) for Service Organizations Osakidetza
Washington, April 9 (ANI): Enzyme replacement therapy (ERT) with agalsidase alfa may slow deterioration of kidney function in men with Fabry disease, provided the treatment is started early, suggests a new study.
The results provide further evidence that ERT with agalsidase alfa may slow the progression of kidney disease, provided that ERT is initiated early in the disease process," said Michael L.
For the study, researchers pooled the results of three previous clinical trials of ERT with agalsidase alfa in 108 men with Fabry disease-a rare genetic disorder.
5 mg" (nonproprietary name: Agalsidase Alfa (Genetic
5 mg Nonproprietary Name: Agalsidase alfa (Genetic Recombination) Dose Form and Strength: Vial preparation, with 3.
Drug Profiles discussed in this report include (migalastat hydrochloride + agalsidase alfa), agalsidase alfa, agalsidase beta biosimilar, agalsidase beta biosimilar, Alpha-Galactosidase, Genz-682452, GZ-402671, JR-051, migalastat hydrochloride, Next Generation biologics for Pompe, Fabry and Hunter, NP-003, PRX-102, Recombinant Enzyme to Replace Alpha-Galactosidase A for Fabry's Disease.