Fenretinide/LXS Oral Powder Plus Ketoconazole in Recurrent Ovarian Cancer

Status Terminated

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

Clinical Trial Details

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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