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Clinical Trial Summary

The purpose of this study is to determine the safety and maximum tolerated dose (MTD) of 90 Y TARE (Y90) in combination with gemcitabine and cisplatin in patients with unresectable intrahepatic cholangiocarcinoma (ICC).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02512692
Study type Interventional
Source Medical University of South Carolina
Contact
Status Active, not recruiting
Phase N/A
Start date July 21, 2015
Completion date August 31, 2022

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