Fabry Disease Treatment Market

Fabry Disease Treatment Market
GLOBAL INDUSTRY INSIGHTS, TRENDS, OUTLOOK, AND
OPPORTUNITY ANALYSIS, 2018-2026
REPORT DESCRIPTION
Fabry Disease Treatment Market– Overview
Fabry disease also called as Anderson-Fabry disease and alpha-galactosidase-A deficiency is an X-linked,
hereditary, lysosomal storage disease caused due to paucity of an enzyme α galactosidase A (an enzyme
required to metabolize lipids, fat-like substances that include oils, waxes, and fatty acids). The mutated
gene leads the formation of lipids to harmful levels in various part of body such as the autonomic nervous
system, cardiovascular system, eyes, and kidneys. Some of the common symptoms of this multisystem
disorder include chronic pain, acroparesthesia, gastrointestinal disturbances, characteristic skin lesions
(angiokeratomata), progressive renal impairment, cardiomyopathy, and stroke.
The presence of robust medication pipeline indicated for treatment of Fabry disease is also expected to be a
major factor fueling growth of global Fabry disease treatment market over the forecast period. Table
mentioned below represents list of some novel therapies in pipeline for Fabry disease treatment.
REPORT DESCRIPTION
Fabry Disease Treatment Market – Taxonomy
By DrugsApproved Drugs
Agalsidase Beta (Fabrazyme/Replagal)
Migalastat (Galafold)
Pipeline Drugs
By Molecule TypeSmall Molecule
Large Molecule (Biologics)
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REPORT DESCRIPTION
Fabry Disease Treatment Market– Key Players
Amicus Therapeutics Inc., Sanofi Genzyme (Sanofi S.A. company),
Idorsia Pharmaceuticals Ltd., Protalix BioTherapeutics, Inc.,
AvroBio Inc., JCR Pharmaceuticals Co., Ltd.,
Resverlogix Corp, and Ozmosis Research Inc.
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The mutated gene leads the formation of lipids to harmful levels in various part of body such as the autonomic nervous system, cardiovascular system, eyes, and kidneys.

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