The Mucosal Addressin Cell Adhesion Molecule 1 pipeline drugs market research report outlays comprehensive information on the Mucosal Addressin Cell Adhesion Molecule 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 Mucosal Addressin Cell Adhesion Molecule 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 Gastrointestinal, Immunology, Metabolic Disorders, and Dermatology which include the indications Ulcerative Colitis, Crohn’s Disease (Regional Enteritis), Autoimmune Disorders, Rheumatoid Arthritis, Type 1 Diabetes (Juvenile Diabetes), and Atopic Dermatitis (Atopic Eczema). It also reviews key players involved in Mucosal Addressin Cell Adhesion Molecule 1 targeted therapeutics development with respective active and dormant or discontinued products.

The Mucosal Addressin Cell Adhesion Molecule 1 pipeline targets constitutes close to five molecules. Out of which, approximately five molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase I, Preclinical, and Discovery stages are 1, 2, and 2 respectively.

Mucosal Addressin Cell Adhesion Molecule 1 overview

Mucosal Addressin Cell Adhesion Molecule 1 (MAdCAM-1) is a cell adhesion receptor expressed by venule cells in mucosal tissues. It plays a critical role in directing the movement of lymphocytes (a type of white blood cell) into mucosal tissues, including specific areas like the Peyer’s patches in the gut and the lamina propria of the intestines

For a complete picture of Mucosal Addressin Cell Adhesion Molecule 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.