The Cyclin Dependent Kinase 6 pipeline drugs market research report outlays comprehensive information on the Cyclin Dependent Kinase 6 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 Cyclin Dependent Kinase 6 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, Infectious Disease, Hematological Disorders, and Toxicology which include the indications Solid Tumor, Human Epidermal Growth Factor Receptor 2 Negative Breast Cancer (HER2- Breast Cancer), Coronavirus Disease 2019 (COVID-19), Human Immunodeficiency Virus (HIV) Infections (AIDS), Hemophagocytic Lymphohistiocytosis, and Chemotherapy-Induced Diarrhea (CID). It also reviews key players involved in Cyclin Dependent Kinase 6 targeted therapeutics development with respective active and dormant or discontinued products.
The Cyclin Dependent Kinase 6 pipeline targets constitutes close to 53 molecules. Out of which, approximately 50 molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Pre-Registration, Phase III, Phase II, Phase I, IND/ CTA Filed, Preclinical, and Discovery stages are 5, 8, 8, 11, 3, 12, and 3 respectively. Similarly, the universities portfolio in Preclinical, and Discovery comprises 2, and 1 molecule.
Cyclin Dependent Kinase 6 overview
Cell division protein kinase 6 (CDK6) is an enzyme encoded by the CDK6 gene. It is involved in initiation and maintenance of cell cycle exit during cell differentiation, prevents cell proliferation and regulates negatively cell differentiation. It is required during thymocyte development. It promotes the production of newborn neurons, probably by modulating G1 length, changes in the actin cytoskeleton including loss of stress fibers, and enhanced motility during cell differentiation. It prevents myeloid differentiation by interfering with RUNX1 and reducing its transcription transactivation-activity.
For a complete picture of Cyclin Dependent Kinase 6’s drug pipeline, buy the report here.
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