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Clinical Trial Summary

This study evaluates the clinical benefit of TAS-102 in participants with metastatic urothelial carcinoma who are resistant to cisplatin or carboplatin front-line and checkpoint inhibitors as second line therapy. All participants will receive TAS-102 in oral form twice per day on Days 1-5 and Days 8-12 of each 28 day cycle.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03762161
Study type Interventional
Source University of Kansas Medical Center
Contact KUCC Navigation
Phone 913-588-3671
Email kucc_navigation@kumc.edu
Status Recruiting
Phase Phase 2
Start date January 3, 2019
Completion date January 2024

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