The Phenylalanine 4 Hydroxylase pipeline drugs market research report outlays comprehensive information on the Phenylalanine 4 Hydroxylase 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 Phenylalanine 4 Hydroxylase 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 which include the indications Phenylketonuria (PKU), and Hyperphenylalaninemia. It also reviews key players involved in Phenylalanine 4 Hydroxylase targeted therapeutics development with respective active and dormant or discontinued products.
The Phenylalanine 4 Hydroxylase pipeline targets constitutes close to 16 molecules. Out of which, approximately 15 molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase II, Phase I, Preclinical, and Discovery stages are 2, 4, 6, and 2 respectively. Similarly, the universities portfolio in Discovery comprises 1 molecule.
Phenylalanine 4 Hydroxylase overview
Phenylalanine 4 hydroxylase or Phenylalanine hydroxylase (PAH) is an enzyme that catalyzes the hydroxylation of the aromatic side-chain of phenylalanine to generate tyrosine. The enzyme works with a molecule called tetrahydrobiopterin (BH4) to carry out this chemical reaction. Tyrosine is used to make several types of hormones, certain chemicals that transmit signals in the brain (neurotransmitters), and a pigment called melanin, which gives hair and skin their color.
For a complete picture of Phenylalanine 4 Hydroxylase’s drug pipeline, buy the report here.
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