The Ileal Sodium/Bile Acid Cotransporter pipeline drugs market research report outlays comprehensive information on the Ileal Sodium/Bile Acid Cotransporter 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 Ileal Sodium/Bile Acid Cotransporter 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 Gastrointestinal, Dermatology, and Genetic Disorders which include the indications Primary Sclerosing Cholangitis, Cholestasis, Pruritus, and Alagille Syndrome. It also reviews key players involved in Ileal Sodium/Bile Acid Cotransporter targeted therapeutics development with respective active and dormant or discontinued products.
The Ileal Sodium/Bile Acid Cotransporter pipeline targets constitutes close to eight molecules. Out of which, approximately eight molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Pre-Registration, Filing rejected/ Withdrawn, Phase III, Phase II, and Preclinical stages are 1, 1, 2, 3, and 1 respectively.
Ileal Sodium/Bile Acid Cotransporter overview
Ileal Sodium/Bile Acid Co-transporter is encoded by SLC10A2 gene. It plays a critical role in the sodium-dependent reabsorption of bile acids from the lumen of the small intestine and cholesterol metabolism.
For a complete picture of Ileal Sodium/Bile Acid Cotransporter’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.
