The Tryptophan 2,3 Dioxygenase pipeline drugs market research report outlays comprehensive information on the Tryptophan 2,3 Dioxygenase 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 Tryptophan 2,3 Dioxygenase pipeline by therapy areas, indications, stages, MoA, RoA, molecule type and the key players in the development pipeline. Buy the report here.
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The report also covers products from therapy areas such as Oncology, Genito Urinary System, and Central Nervous System which include the indications Oncology, Solid Tumor, End-Stage Kidney Disease (End-Stage Renal Disease or ESRD), and Parkinson’s Disease. It also reviews key players involved in Tryptophan 2,3 Dioxygenase targeted therapeutics development with respective active and dormant or discontinued products.
The Tryptophan 2,3 Dioxygenase pipeline targets constitutes close to 12 molecules. Out of which, approximately 12 molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase I, Preclinical, and Discovery stages are 3, 7, and 2 respectively.
Tryptophan 2,3 Dioxygenase overview
Tryptophan 2, 3-dioxygenase is an enzyme that plays a critical role in tryptophan metabolism by catalyzing the first and rate-limiting step of the kynurenine pathway. It has specificity towards tryptamine and derivatives including D- and L-tryptophan, 5-hydroxytryptophan and serotonin.
For a complete picture of Tryptophan 2,3 Dioxygenase’s drug pipeline, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
Global Markets Direct’s report features investigational drugs from across globe covering over 20 therapy areas and nearly 3,000 indications. The report is built using data and information sourced from Global Markets Direct’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations and featured press releases from company/university sites and industry-specific third-party sources.
Drug profiles featured in the report undergo periodic review following a stringent set of processes to ensure that all the profiles are updated with the latest set of information. Additionally, various dynamic tracking processes ensure that the most recent developments are captured on a real time basis.
