The Ectonucleoside Triphosphate Diphosphohydrolase 1 pipeline drugs market research report outlays comprehensive information on the Ectonucleoside Triphosphate Diphosphohydrolase 1 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 Ectonucleoside Triphosphate Diphosphohydrolase 1 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, Immunology, and Cardiovascular which include the indications Solid Tumor, Unspecified Cancer, Autoimmune Disorders, Inflammation, Coronary Artery Disease (CAD) (Ischemic Heart Disease), and Stroke. It also reviews key players involved in Ectonucleoside Triphosphate Diphosphohydrolase 1 targeted therapeutics development with respective active and dormant or discontinued products.
The Ectonucleoside Triphosphate Diphosphohydrolase 1 pipeline targets constitutes close to 20 molecules. Out of which, approximately 20 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, 7, 5, and 6 respectively.
Ectonucleoside Triphosphate Diphosphohydrolase 1 overview
ENTPD1 is a plasma membrane protein that hydrolyzes extracellular ATP and ADP to AMP. Inhibition of this protein’s activity may confer anticancer benefits. Several transcript variants encoding different isoforms have been found for this gene.
For a complete picture of Ectonucleoside Triphosphate Diphosphohydrolase 1’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.
