The purpose of this project is to see if weekly carboplatin compared with phenoxodiol in combination with weekly carboplatin, is effective against late stage ovarian cancer and to see what, if any, side-effects of treatment may result.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
142
400mg phenoxodiol three times daily in 28 day cycles.
AUC=2 weekly in 28 day cycles
every 8 hours daily in 28 day cycles
The primary efficacy end-point is progression-free survival (PFS). PFS is the time from randomization until disease progression or death
Time frame: Progression Free Survival
The secondary efficacy end-point is overall survival (OS)
Time frame: Overall survival
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