The Sodium/Glucose Cotransporter 1 pipeline drugs market research report outlays comprehensive information on the Sodium/Glucose Cotransporter 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 Sodium/Glucose Cotransporter 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 Metabolic Disorders, Cardiovascular, Gastrointestinal, and Genito Urinary System which include the indications Type 2 Diabetes, Diabetes, Congestive Heart Failure (Heart Failure), Hypertrophic Cardiomyopathy, Constipation, Gastroparesis, and Diabetic Nephropathy. It also reviews key players involved in Sodium/Glucose Cotransporter 1 targeted therapeutics development with respective active and dormant or discontinued products.

The Sodium/Glucose Cotransporter 1 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, and Preclinical stages are 2, 4, 3, and 4 respectively.

Sodium/Glucose Cotransporter 1 overview

Sodium/glucose cotransporter 1 (SLC5A1) is an electrogenic Na+-coupled sugar simporter that actively transports D-glucose or D-galactose at the plasma membrane, with a Na+ to sugar coupling ratio of 2:1. Transporter activity is driven by a transmembrane Na+ electrochemical gradient set by the Na+/K+ pump. It has a primary role in the transport of dietary monosaccharides from enterocytes to blood.

For a complete picture of Sodium/Glucose Cotransporter 1’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.