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Clinical Trial Summary

The purpose of this study is to make a preliminary assessment of the efficacy of a combined APR-246 and carboplatin/PLD chemotherapy regimen, compared with carboplatin/PLD chemotherapy regimen alone, in patients with platinum sensitive recurrent high grade serous ovarian cancer (HGSOC) with mutated p53. In addition, the study aims to assess the safety profile of the combined APR-246 and carboplatin/PLD chemotherapy regimen compared with carboplatin/PLD chemotherapy regimen alone, to evaluate potential biomarkers, and to assess the biological activity in tumor and surrogate tissues. The trial will enroll up to a maximum of 400 patients.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT02098343
Study type Interventional
Source Aprea Therapeutics
Contact
Status Completed
Phase Phase 1/Phase 2
Start date March 2014
Completion date April 2019