drugset / Trial / NCT01607957

Study of TAS-102 in Patients With Metastatic Colorectal Cancer Refractory to Standard Chemotherapies

NCT01607957 ↗

Phase 3 Completed 800 enrolled Taiho Oncology, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to compare the efficacy and safety of TAS-102 versus placebo in patients with refractory metastatic colorectal cancer.

Timeline

Start
2012-06-17
Primary completion
2014-01-31
Completion
2016-05-23

Outcome

Met primary endpoint

registry TAS-102 vs Placebo; p <0.0001; Hazard Ratio (HR) 0.68 (95% CI 0.58 to 0.81); Stratified log-rank test NCT01607957 ↗

paper The median overall survival improved from 5.3 months with placebo to 7.1 months with TAS-102 PMID 25970050 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tipiracil Small molecule — Oral
Subject Trifluridine Small molecule — Oral

Indications