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Clinical Trial Summary

The purpose of this study is to determine the effectiveness of fenretinide (4-HPR/LXS) plus ketoconazole in the treatment of recurrent ovarian cancer or primary peritoneal carcinoma. In addition, researchers would like to determine if the drugs are most effective together or if fenretinide (4-HPR/LXS) is most effective alone.


Clinical Trial Description

In this study, an initial Phase I component of six patients will be conducted to monitor for potential toxicities as this wil be the initial adult experience of fenretinide (4-HPR) given together with ketoconazole ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01535157
Study type Interventional
Source South Plains Oncology Consortium
Contact
Status Terminated
Phase Phase 1/Phase 2
Start date February 2012
Completion date June 2017

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