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|Therapy Name||CGM097 + Dabrafenib + Navitoclax + PF-04217903|
|Drug Name||Trade Name||Synonyms||Drug Classes||Drug Description|
|CGM097||NVP-CGM097||MDM2 Inhibitor 22||CGM097 binds to the p53 binding region of MDM2 and prevents MDM2-p53 interaction, resulting in activation of p53 signaling and decreased tumor growth (Cancer Res October 1, 2014 74:4638, PMID: 32651541).|
|Dabrafenib||Tafinlar||GSK2118436||BRAF Inhibitor 24||Tafinlar (dabrafenib) inhibits the activity of BRAF, including V600E, which results in the inhibition of tumor cell proliferation (PMID: 22735384). Tafinlar (dabrafenib) is FDA approved for BRAF V600E/K- positive unresectable or metastatic melanoma, and in combination with Mekinist (trametinib) for BRAF V600E/K-mutant melanoma, BRAF V600E-mutant non-small cell lung cancer, BRAF V600E-mutant anaplastic thyroid cancer, for adult and pediatric patients of 6 years or older with unresectable or metastatic solid tumors harboring BRAF V600E, and for pediatric patients of 1 year or older with low-grade glioma harboring BRAF V600E (FDA.gov).|
|Navitoclax||ABT-263||BCL-XL inhibitor 14 BCL2 inhibitor 26||Navitoclax (ABT-263) is a BCL2, BCL-XL, and BCL-W inhibitor, which may enhance the efficacy of chemotherapeutics (PMID: 25787766, PMID: 32513939).|
|PF-04217903||PF04217903||MET Inhibitor 58||PF-04217903 binds to MET and inhibits its activation, resulting in decreased activation of downstream signaling, and potentially resulting in decreased tumor cell growth and migration and increased tumor cell death (PMID: 28599617).|
|Molecular Profile||Indication/Tumor Type||Response Type||Therapy Name||Approval Status||Evidence Type||Efficacy Evidence||References|
|BRAF mut TP53 wild-type||colorectal cancer||sensitive||CGM097 + Dabrafenib + Navitoclax + PF-04217903||Preclinical - Cell culture||Actionable||In a preclinical study, the combination of Navitoclax (ABT-263), CGM097, Tafinlar (dabrafenib), and PF04217903 resulted in the greatest synergistic effect and inhibition of cell growth in colorectal cancer cells harboring a BRAF mutation and wild-type TP53 in culture compared to the double or triple combinations of the therapies (PMID: 27659046).||27659046|
|Clinical Trial||Phase||Therapies||Title||Recruitment Status||Covered Countries||Other Countries|