The Coagulation Factor X pipeline drugs market research report outlays comprehensive information on the Coagulation Factor X 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 Coagulation Factor X 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 Cardiovascular, Hematological Disorders, Central Nervous System, and Infectious Disease which include the indications Deep Vein Thrombosis (DVT), Venous Thromboembolism, Bleeding And Clotting Disorders, Hemophilia A (Factor VIII Deficiency), Brain Hemorrhage, and Sepsis. It also reviews key players involved in Coagulation Factor X targeted therapeutics development with respective active and dormant or discontinued products.
The Coagulation Factor X pipeline targets constitutes close to 43 molecules. Out of which, approximately 38 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 The molecules developed by companies in Pre-Registration, Filing rejected/ Withdrawn, Phase III, Phase II, Phase I, IND/ CTA Filed, and Preclinical stages are 1, 1, 7, 3, 7, 5, and 13 respectively. Similarly, the universities portfolio in Phase II, Preclinical, and Discovery comprises 1, 3, and 1 molecule.
Coagulation Factor X overview
Factor Xa is a vitamin K-dependent glycoprotein that converts prothrombin to thrombin in the presence of factor Va, calcium, and phospholipid during blood clotting.
For a complete picture of Coagulation Factor X’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.
