drugset / Trial / NCT02025803

A Safety, Tolerability and Pharmacokinetic Study of TAS-114 in Combination With Capecitabine in Patients With Advanced Solid Tumors

NCT02025803

Phase 1 Completed 60 enrolled Taiho Oncology, Inc. Quintiles, Inc. · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this exploratory study is to investigate the safety and determine the maximum tolerated dose (MTD) of TAS-114 in combination with capecitabine in patients with advanced solid tumors for which the patients have no available therapy likely to convey clinical benefit.

Timeline

Start
2012-11
Primary completion
2017-07-07
Completion
2017-07-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 760 mg/m2 Oral
Subject TAS-114 Unknown 20 mg/m2 Oral
Subject TAS-114 Unknown 480 mg/m2 Oral

Indications