The Lysosomal Alpha Glucosidase pipeline drugs market research report outlays comprehensive information on the Lysosomal Alpha Glucosidase targeted therapeutics, complete with analysis by indications, stage of development, mechanism of action (MoA), route of administration (RoA), and molecule type. GlobalData’s report assesses the drugs in the Lysosomal Alpha Glucosidase pipeline by therapy areas, indications, stages, MoA, RoA, molecule type and the key players in the development pipeline. Buy the report here.
The report also covers products from therapy areas such as Metabolic Disorders, and Central Nervous System which include the indications Pompe Disease, and Lafora Disease (Unverricht Disease). It also reviews key players involved in Lysosomal Alpha Glucosidase targeted therapeutics development with respective active and dormant or discontinued products.
The Lysosomal Alpha Glucosidase pipeline targets constitutes close to 22 molecules. Out of which, approximately 19 molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase III, Phase II, Preclinical, and Discovery stages are 2, 4, 9, and 4 respectively. Similarly, the universities portfolio in Phase I, and Preclinical comprises 1, and 2 molecule.
Lysosomal Alpha Glucosidase overview
Lysosomal alpha-glucosidase is an enzyme encoded by the GAA gene. It is essential for the degradation of glygogen to glucose in lysosomes. Defects in this gene lead to glycogen storage disease II or Pompe disease.
For a complete picture of Lysosomal Alpha Glucosidase’s drug pipeline, buy the report here.
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