The Stromal Cell Derived Factor 1 pipeline drugs market research report outlays comprehensive information on the Stromal Cell Derived Factor 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 Stromal Cell Derived Factor 1 pipeline by therapy areas, indications, stages, MoA, RoA, molecule type and the key players in the development pipeline. Buy the report here.
The report also covers products from therapy areas such as Oncology, Immunology, Dermatology, and Undisclosed which include the indications Oncology, Metastatic Pancreatic Cancer, WHIM Syndrome (Warts, Hypogammaglobulinemia, Infections and Myelokathexis), Pancreatic Islet Transplant Rejection, Diabetic Foot Ulcers, Wounds, and Unspecified. It also reviews key players involved in Stromal Cell Derived Factor 1 targeted therapeutics development with respective active and dormant or discontinued products.
The Stromal Cell Derived Factor 1 pipeline targets constitutes close to nine molecules. Out of which, approximately seven molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase II, Preclinical, and Discovery stages are 2, 1, and 3 respectively. Similarly, the universities portfolio in Preclinical, and Discovery comprises 1, and 1 molecule.
Stromal Cell Derived Factor 1 overview
Stromal cell-derived factor 1 (SDF1) or C-X-C motif chemokine 12 (CXCL12) is a chemokine protein encoded by the CXCL12 gene. It activates the C-X-C chemokine receptor CXCR4 to induce a rapid and transient rise in the level of intracellular calcium ions and chemotaxis. It binds to atypical chemokine receptor ACKR3, which activates the beta-arrestin pathway and acts as a scavenger receptor for SDF-1. It acts as a positive regulator of monocyte migration and a negative regulator of monocyte adhesion via the LYN kinase. It stimulates migration of monocytes and T-lymphocytes through its receptors, CXCR4 and ACKR3, and decreases monocyte adherence to surfaces coated with ICAM-1.
For a complete picture of Stromal Cell Derived Factor 1’s drug pipeline, buy the report here.
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