The Vasopressin V2 Receptor pipeline drugs market research report outlays comprehensive information on the Vasopressin V2 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 Vasopressin V2 Receptor 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 Cardiovascular, Genito Urinary System, Genetic Disorders, and Gastrointestinal which include the indications Congestive Heart Failure (Heart Failure), Edema, Nocturia, Enuresis, Polycystic Kidney Disease, and Hepatorenal Syndrome. It also reviews key players involved in Vasopressin V2 Receptor targeted therapeutics development with respective active and dormant or discontinued products.
The Vasopressin V2 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 III, Phase II, Phase I, and Preclinical stages are 2, 4, 1, 2, and 4 respectively.
Vasopressin V2 Receptor overview
Vasopressin receptor type 2 (AVPR2), also known as the V2 receptor, belongs to the G protein-coupled receptor (GPCR) superfamily and couples to Gs, thus stimulating adenylate cyclase. The V2 receptor is expressed in the kidney tubule, predominantly in the distal convoluted tubule and collecting ducts, where its primary property is to respond to the pituitary hormone arginine vasopressin (AVP) by stimulating mechanisms that concentrate the urine and maintain water homeostasis in the organism.
For a complete picture of Vasopressin V2 Receptor’s drug pipeline, buy the report here.
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