Tinengotinib, a selective multi-kinase inhibitor, effectively targets FGFR2 fusion/rearrangement and resistance mutations in early trials involving cholangiocarcinoma patients.
Tasurgratinib (E7090) is an orally available selective inhibitor of FGFR 1–3, the recommended dose is 140 mg per day per the dose-escalation part of a first-in-human phase 1 study.
The phase II trial of mFOLFIRINOX, followed by hepatic infusion of floxuridine & dexamethasone with mFOLFIRI as first-line treatment in intrahepatic cholangiocarcinoma patients (HELIX-1), was presented at 2024 ASCO_GI on Jan 18.
Based on previous studies, biomarker analysis from Phase 1/2 study of tusamitamab ravtansine (SAR408701) in patients with advanced non-small cell lung cancer (NSCLC) was reported at the AACR Congress.