In addition, it has an exclusive licensing agreement to commercialize Hunterase, an
enzyme replacement therapy for the treatment of Hunter syndrome, developed by GC Pharma and marketed in more than ten countries worldwide.
Eight-year clinical outcomes of long-term
enzyme replacement therapy for 884 children with Gaucher disease type 1.
Fabry disease:
enzyme replacement therapy in [alpha]-galactosidase A deficient mice.
Successful pregnancy and lactation outcome in a patient with Gaucher disease receiving
enzyme replacement therapy, and the subsequent distribution and excretion of imiglucerase in human breast milk.
The
enzyme replacement therapy that Maura begins on Monday is her best hope.
Will began
Enzyme Replacement Therapy into his body about five years ago.
Dr Chris Hendriksz, a consultant at Birmingham Children's Hospital who specialises in Inherited Metabolic Disorders, said he believed the
enzyme replacement therapy slows down progression of the disease.
After
enzyme replacement therapy (ERT), her symptoms and clinical and laboratory findings significantly improved.
The CUPID trial (Calcium Up-regulation by Percutaneous administration of gene therapy In cardiac Disease) is a randomized, double-blind, placebo-controlled study to assess the efficacy and safety of MYDICAR, a genetically targeted
enzyme replacement therapy for advanced heart failure.
Tokyo, Dec 24, 2009 - (JCN Newswire) - A New Drug Application for the pancreatic
enzyme replacement therapy agent for pancreatic exocrine insufficiency, SA-001 (API name: Pancrelipase) that Solvay Seiyaku K.
Enzyme replacement therapy has been successful in treating one form of lysosomal storage disease called Gaucher disease.