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Clinical Trial Summary

This is a randomized, open-label, Phase 2 study of TAS-114 administered in combination with S-1, to investigate the efficacy, safety and tolerability of the TAS-114/S-1 regimen in patients with advanced or metastatic NSCLC. The study will be conducted internationally in 2 regions: Asian [Japan] and Western [Europe and US]. Patients will be randomized into TAS-114/S-1 arm versus S-1 control arm in a 1:1 ratio.


Clinical Trial Description

Randomization will take place once the consented patient has completed all the necessary baseline procedures and is deemed eligible for study entry. Treatment assignment will be done centrally using a dynamic allocation method (biased coin) via an interactive voice/web response system (IXRS) stratified by: - Geographical region (Region 1: Asian [Japan]; Region 2: Western [Europe and US]) - Histological subtypes (nonsquamous cell carcinoma [including mixed] and squamous cell carcinoma) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02855125
Study type Interventional
Source Taiho Oncology, Inc.
Contact
Status Completed
Phase Phase 2
Start date August 29, 2016
Completion date November 30, 2017

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