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  • aldurazyme
  • brineura
  • entero
  • vimizim

Enzyme Replacement Therapy Equipment Supplied In Usa California

4 equipment items found
In CaliforniaAvailable In CaliforniaNear California

Vimizim - Model MPS IVA - Elosulfase Alfa for Morquio A Syndrome

Vimizim - Model MPS IVA - Elosulfase Alfa for Morquio A Syndrome

Manufactured by:BioMarin   based inSan Rafael, CALIFORNIA (USA)
Vimizim (elosulfase alfa) is the first approved enzyme replacement therapy designed to address the underlying cause of Morquio A syndrome, or mucopolysaccharidosis IVA (MPS IVA) — a deficiency in the enzyme N-acetylgalactosamine-6 sulfatase (GALNS). VIMIZIM works at a cellular level to help with deficient ...
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Brineura - Cerliponase Alfa for Neuronal Ceroid Lipofuscinosis Type 2 CLN2 Disease

Brineura - Cerliponase Alfa for Neuronal Ceroid Lipofuscinosis Type 2 CLN2 Disease

Manufactured by:BioMarin   based inSan Rafael, CALIFORNIA (USA)
Brineura (cerliponase alfa) is indicated to slow the loss of ambulation in symptomatic pediatric patients 3 years of age and older with late infantile neuronal ceroid lipofuscinosis type 2 (CLN2), also known as tripeptidyl peptidase 1 (TPP1) deficiency. Brineura is the first enzyme replacement therapy to be directly administered into the fluid of ...
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Entero - Model FW-EPI - Recombinant Lipase Enzyme

Entero - Model FW-EPI - Recombinant Lipase Enzyme

Manufactured by:Entero Therapeutics, Inc.   based inBoca Raton, FLORIDA (USA)
FW-EPI (adrulipase) is a recombinant lipase enzyme administered as an oral, non-systemic biologic capsule for the treatment of exocrine pancreatic insufficiency (EPI) associated with cystic fibrosis (CF) and chronic pancreatitis (CP). Adrulipase is derived from the Yarrowia lipolytica yeast lipase and is designed to break up fat molecules in the digestive tract of EPI patients so that they can be ...
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Aldurazyme - Aldurazyme - Laronidase for MPS I

Aldurazyme - Aldurazyme - Laronidase for MPS I

Manufactured by:BioMarin   based inSan Rafael, CALIFORNIA (USA)
ALDURAZYME (laronidase) is indicated for patients with Hurler and Hurler-Scheie forms of mucopolysaccharidosis I (MPS I) and for patients with the Scheie form who have moderate to severe symptoms. The risks and benefits of treating mildly affected patients with the Scheie form have not been established. ALDURAZYME has been shown to improve pulmonary function and walking capacity. ALDURAZYME has ...
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