The Endothelin B Receptor pipeline drugs market research report outlays comprehensive information on the Endothelin B Receptor 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 Endothelin B Receptor 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, Cardiovascular, Central Nervous System, and Ophthalmology which include the indications Glioblastoma Multiforme (GBM), Ovarian Cancer, Pulmonary Arterial Hypertension, Acute Ischemic Stroke, Alzheimer’s Disease, Hypoxic-Ischemic Encephalopathy, and Diabetic Retinopathy. It also reviews key players involved in Endothelin B Receptor targeted therapeutics development with respective active and dormant or discontinued products.

The Endothelin B Receptor pipeline targets constitutes close to 13 molecules. Out of which, approximately 13 molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Pre-Registration, Phase II, Phase I, Preclinical, and Discovery stages are 3, 2, 1, 3, and 4 respectively.

Endothelin B Receptor overview

Endothelin receptor type B (EDNRB) is a G protein-coupled receptor that activates a phosphatidylinositol-calcium second messenger system. Its ligand, endothelin, consists of a family of three potent vasoactive peptides: ET1, ET2, and ET3. In melanocytic cells the EDNRB gene is regulated by the microphthalmia-associated transcription factor.

For a complete picture of Endothelin B Receptor’s drug pipeline, buy the report here.

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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.