Table 1.
Company | Compound | Target(s) | Indication | Clinical status |
---|---|---|---|---|
Servier | S49076 (kinase inhibitor) | MET, AXL, FGFR1/2/3 | Advanced solid tumors | Phase I 2013-003079-37 |
Mirati Therapeutics Inc. | MGCD516 (kinase inhibitor) | MET, AXL, and members of the VEGFR, PDGFR, DDR2, TRK, and Eph families | Advanced solid tumors | Phase I NCT02219711 |
Mirati Therapeutics Inc. | MGCD265 (kinase inhibitor) | MET/AXL | Advanced malignancies | Phase I NTC00697632 |
Betta Pharmaceuticals Co., Ltd | BPI-9016M (kinase inhibitor) | MET/AXL | Advanced solid tumors | Phase I NCT02478866 |
BerGenBio AS | BGB324 (R428; kinase inhibitor) | AXL | NSCLC and AML | Phase I/II NCT02488408 NCT02424617 |
Tolero Pharmaceuticals and Astex Pharmaceuticals | TP-0903 (kinase inhibitor) | AXL | Pancreatic cancer, lung cancer | Preclinical |
Abbreviations: AML, acute myelogenous leukemia; DDR, discoidin domain receptor; Eph, ephrin; FGFR, fibroblast growth factor receptor; PDGFR, platelet-derived growth factor receptor; TRK, tropomyosin receptor kinase.