drugset / Trial / NCT02052778

A Study of TAS-120 in Patients With Advanced Solid Tumors

NCT02052778

Phase 1/2 Completed 407 enrolled Taiho Oncology, Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

This is an open-label, nonrandomized, Phase 1/2 study for the fibroblast growth factor receptor (FGFR) inhibitor futibatinib (TAS-120). The purpose of the study is to evaluate the safety, tolerability, pharmacokinetic, pharmacodynamic, and anti-tumor activity of futibatinib in patients with advanced solid tumors with and without genomic FGF/FGFR abnormalities. The study will be conducted in 3 parts: 1. Dose escalation portion to determine the -Maximum Tolerated Dose and/ or Recommended Phase 2 Dose of futibatinib. 2. Phase 1 expansion portion to further evaluate the safety and efficacy of futibatinib in patients with tumors harboring FGF/FGFR aberrations, including patients with cholangiocarcinoma (CCA), primary central nervous system tumors, urothelial carcinoma, breast cancer, gastric cancer. 3. Phase 2 study portion to confirm objective response rate of futibatinib in intrahepatic CCA patients with tumors harboring FGFR2 gene rearrangements (incl fusions).

Timeline

Start
2014-07-21
Primary completion
2020-10-01
Completion
2024-10-22

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Futibatinib Small molecule 4 mg Oral
Subject Futibatinib Small molecule 8 mg Oral
Subject Futibatinib Small molecule 16 mg Oral
Subject Futibatinib Small molecule 20 mg Oral
Subject Futibatinib Small molecule 24 mg Oral
Subject Futibatinib Small molecule 36 mg Oral
Subject Futibatinib Small molecule 56 mg Oral
Subject Futibatinib Small molecule 80 mg Oral
Subject Futibatinib Small molecule 120 mg Oral
Subject Futibatinib Small molecule 160 mg Oral
Subject Futibatinib Small molecule 200 mg Oral