NRG-GY005

A Randomized Phase II/III study of the combination of Cediranib and Olaparib compared to Cediranib or Olaparib alone, or Standard of care chemotherapy in women with recurrent platinum-resistant or -refractory ovarian, fallopian tube, or primary peritoneal cancer (COCOS).

Principal Investigator

Jung-Min Lee, MD

Status

Closed to Accrual

Disease Site

Gynecologic [GY]

Ovarian

Phase

II/III

Developmental Therapeutics

No

Primary Objective

Phase II
To assess the efficacy and identify (in)active arm(s) of the combination of cediranib and olaparib, cediranib alone, olaparib alone, and physician's choice standard of care chemotherapy, as measured by PFS in the setting of recurrent platinum-resistant or-refractory ovarian, primary peritoneal or fallopian tube cancer.

Phase III
To assess the efficacy of the combination of cediranib and olaparib, and active monotherapy experimental arm(s) from Randomized Phase II, as measured by OS and PFS, as compared to physician's choice standard of care chemotherapy in women with recurrent platinum-resistant or-refractory ovarian, primary peritoneal or fallopian tube cancer.

Patient Population

Patients has histologically or cytologically confirmed ovarian cancer, peritoneal cancer or fallopian tube cancer with histological diagnosis of either serous or endometrioid cancer based on local histopathological findings. Both endometrioid and serous histology will be high-grade for eligibility of non-mutation carriers. Participants with a deleterious germline BRCA-mutation on a commercial CLIA assay with other high-grade histologies, including clear cell, transitional cell, undifferentiated adenocarcinoma, mixed epithelial adenocarcinoma are also eligible. 

Target Accrual

208