The purpose of this study is to evaluate the effect of OPT-822/OPT-821 on improving Progression-Free Survival (PFS) in subjects who have non-progressive epithelial ovarian, fallopian tube, or primary peritoneal cancer after cytoreductive surgery and platinum-based chemotherapy as initial treatment for primary disease or as salvage treatment for first relapse.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
110
Mackay Memorial Hospital
Taipei, Taiwan
RECRUITINGProgression Free Survival (PFS)
Time frame: Until disease progression or up to 5 years after the enrollment
Disease Recurrence Rate
Time frame: At 2 years after the enrollment
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