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|Therapy Name||AVB-S6-500 + Cabozantinib|
|Drug Name||Trade Name||Synonyms||Drug Classes||Drug Description|
|AVB-S6-500||AVBS6500|AV S6 500||AVB-S6-500 is a fusion protein comprised of human IgG1 linked to the extracellular domain of Axl, which binds to growth arrest-specific protein 6 (GAS6), potentially resulting in decreased downstream signaling and reduced tumor growth (PMID: 32148495, PMID: 31599479).|
|Cabozantinib||Cometriq||Cabometyx|Cabozantinib-s-malate|XL184||AXL Inhibitor 29 FLT3 Inhibitor 61 KIT Inhibitor 55 MET Inhibitor 56 RET Inhibitor 48 ROS1 Inhibitor 19 VEGFR2 Inhibitor 36||Cometriq (Cabometyx, cabozantinib) inhibits several receptor tyrosine kinases, including VEGFR2, FLT3, AXL, MET, RET, ROS1 fusions, and c-KIT (PMID: 27370605, PMID: 21926191). Cometriq (cabozantinib) is FDA approved for use in patients with medullary thyroid cancer, Cabometyx (cabozantinib) is FDA approved for use in patients with advanced renal cell carcinoma, hepatocellular carcinoma previously treated with sorafenib, adult and pediatric patients 12 years and older with locally advanced or metastatic differentiated thyroid cancer, and in combination with Opdivo (nivolumab) in patients with advanced renal cell carcinoma (FDA.gov).|
|Molecular Profile||Indication/Tumor Type||Response Type||Therapy Name||Approval Status||Evidence Type||Efficacy Evidence||References|
|Clinical Trial||Phase||Therapies||Title||Recruitment Status||Covered Countries||Other Countries|
|NCT04300140||Phase Ib/II||AVB-S6-500 + Cabozantinib Cabozantinib||Efficacy and Safety Study of AVB-S6-500 in Patients With Clear Cell Renal Cell Carcinoma||Active, not recruiting||USA||0|