The Vascular Endothelial Growth Factor D pipeline drugs market research report outlays comprehensive information on the Vascular Endothelial Growth Factor D 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 Vascular Endothelial Growth Factor D 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 Oncology, Ophthalmology, and Cardiovascular which include the indications Solid Tumor, Oncology, Diabetic Macular Edema, Wet (Neovascular / Exudative) Macular Degeneration, and Refractory Angina. It also reviews key players involved in Vascular Endothelial Growth Factor D targeted therapeutics development with respective active and dormant or discontinued products.

The Vascular Endothelial Growth Factor D 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 III, Phase II, and Preclinical stages are 1, 1, and 3 respectively.

Vascular Endothelial Growth Factor D overview

Vascular Endothelial Growth Factor D is a member of the PDGF/VEGF family and is active in angiogenesis, lymphangiogenesis, and endothelial cell growth. This secreted protein undergoes a complex proteolytic maturation, generating multiple processed forms which bind and activate VEGFR-2 and VEGFR-3 receptors. This protein is structurally and functionally similar to vascular endothelial growth factor C.

For a complete picture of Vascular Endothelial Growth Factor D’s drug pipeline, buy the report here.

This content was updated on 25 January 2024

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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.