The Coagulation Factor VII pipeline drugs market research report outlays comprehensive information on the Coagulation Factor VII 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 VII 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 Hematological Disorders, Cardiovascular, Central Nervous System, and Other Diseases which include the indications Hemophilia, Bleeding And Clotting Disorders, Thrombosis, Ischemia Reperfusion Injury, Brain Hemorrhage, and Trauma. It also reviews key players involved in Coagulation Factor VII targeted therapeutics development with respective active and dormant or discontinued products.
The Coagulation Factor VII pipeline targets constitutes close to 20 molecules. Out of which, approximately 18 molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase III, Phase II, Phase I, IND/ CTA Filed, Preclinical, and Discovery stages are 4, 1, 2, 1, 7, and 3 respectively. Similarly, the universities portfolio in Phase II, and Preclinical comprises 1, and 1 molecule.
Coagulation Factor VII overview
Coagulation factor VII is a coagulation protease responsible for starting a cascade of proteolytic events that lead to thrombin generation, fibrin deposition, and platelet activation. FVII is a wide used target for clinical anti-coagulant applications.
For a complete picture of Coagulation Factor VII’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.
