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Clinical Trial Summary

The purpose of this study is to determine the maximum tolerated dose of the combination of vorinostat, cisplatin, pemetrexed, and radiation therapy in patients with unresectable stage IIIA/IIIB non-small cell lung cancer.


Clinical Trial Description

This phase I trial will escalate doses of the histone deacetylase inhibitor (HDAC) vorinostat to a chemoradiation platform for cisplatin, pemetrexed and radiation to a dose of 70Gy in NSCLC patients with unresectable IIIA and dry IIIB disease. The endpoint will be to determine MTD of the combination. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01059552
Study type Interventional
Source Fox Chase Cancer Center
Contact
Status Completed
Phase Phase 1
Start date December 16, 2009
Completion date October 21, 2019

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