The CD276 Antigen pipeline drugs market research report outlays comprehensive information on the CD276 Antigen 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 CD276 Antigen 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, and Undisclosed which include the indications Solid Tumor, Non-Small Cell Lung Cancer, and Unspecified. It also reviews key players involved in CD276 Antigen targeted therapeutics development with respective active and dormant or discontinued products.
The CD276 Antigen pipeline targets constitutes close to 97 molecules. Out of which, approximately 76 molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase III, Phase II, Phase I, Phase 0, IND/ CTA Filed, Preclinical, and Discovery stages are 1, 13, 11, 2, 3, 31, and 15 respectively. Similarly, the universities portfolio in Phase II, Phase I, Phase 0, Preclinical, and Discovery comprises 5, 6, 1, 5, and 4 molecule.
CD276 Antigen overview
CD276 antigen, also known as B7-H3, is a cell surface protein that plays a role in regulating immune responses. It is a member of the B7 family of immune checkpoint molecules, which includes proteins that interact with receptors on immune cells to regulate immune responses.
For a complete picture of CD276 Antigen’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.
