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Durvalumab Treatment in Combination With Chemotherapy and Bevacizumab, Followed by Maintenance Durvalumab, Bevacizumab and Olaparib Treatment in Advanced Ovarian Cancer Patients.

Trial Status: Active

This is a Phase III randomised, double-blind, multi-centre study to evaluate the efficacy and safety of durvalumab in combination with standard of care platinum based chemotherapy and bevacizumab followed by maintenance durvalumab and bevacizumab or durvalumab, bevacizumab and olaparib in patients with newly diagnosed advanced ovarian cancer.

Inclusion Criteria

  • Key Inclusion Criteria: Female patients with newly diagnosed, histologically confirmed, advanced (Stage III-IV) high grade epithelial ovarian cancer including high grade serious, high grade endometriod, clear cell ovarian cancer or carcinosarcoma, primary peritoneal cancer and / or fallopian-tube cancer - Patients must be aged ≥18 years of age. For patients enrolled in Japan that are aged <20 year - All patients should be candidates for cytoreductive surgery either: upfront primary surgery OR plan to undergo chemotherapy with interval debulking surgery - Evidence of presence or absence of BRCA1/2 mutation in tumour tissue - Mandatory provision of tumour sample for centralised tBRCA testing - ECOG performance status 0-1 - Patients must have preserved organ and bone marrow function - Postmenopausal or evidence of non-childbearing status for women of childbearing potential: negative urine or serum pregnancy test Key Exclusion Criteria: Non-epithelial ovarian cancer, borderline tumors, low grade epithelial tumors or mucinous histology - Prior systemic anti-cancer therapy for ovarian cancer - Inability to determine the presence or absence of a deleterious or suspected deleterious BRCA mutation - Prior treatment with PARP inhibitor or immune mediated therapy - Planned intraperitoneal cytotoxic chemotherapy - Active or prior documented autoimmune or inflammatory disorders - Patients considered a poor medical risk due to a serious, uncontrolled intercurrent illness - Clinically significant cardiovascular disease - Patients with known brain metastases - History of another primary malignancy except for: - Malignancy treated with curative intent and with no known active disease ≥5 years before the first dose of study treatment and of low potential risk for recurrence (patients who have received prior adjuvant chemotherapy for early stage breast cancer may be eligible, provided that it was completed ≥3 years prior to registration, and that the patient remains free of recurrent or metastatic disease) - Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease - Adequately treated carcinoma in situ without evidence of disease - Endometrial cancer FIGO Stage IA, Grade 1 or Grade 2 - Persistent toxicities CTCAE Grade >2 caused by previous cancer therapy - Patients with a known hypersensitivity to olaparib, durvalumab or any of the excipients of these products and to the combination/comparator agents - Breast feeding women


Los Angeles
UCLA / Jonsson Comprehensive Cancer Center
Contact: Ross Mar Divinagracia
Phone: 310-825-0580
San Francisco
UCSF Medical Center-Mount Zion
Status: ACTIVE
Contact: Helen Diller Family Comprehensive Cancer Center
Phone: 877-827-3222


University of Colorado Hospital


Moffitt Cancer Center


Indiana University / Melvin and Bren Simon Cancer Center
Contact: Seth Burns
Phone: 317-278-5238

New York

New York
Memorial Sloan Kettering Cancer Center
Status: ACTIVE

North Carolina

Duke University Medical Center
Status: ACTIVE


Case Comprehensive Cancer Center
Ohio State University Comprehensive Cancer Center


Thomas Jefferson University Hospital
University of Pennsylvania / Abramson Cancer Center
Willow Grove
Abington Memorial Hospital-Asplundh Cancer Pavilion


Salt Lake City
Huntsman Cancer Institute / University of Utah
Status: ACTIVE

Eligible patients will be those patients with newly diagnosed, histologically confirmed advanced (Fédération Internationale de Gynécologie et d'Obstétrique [FIGO] Stage III-IV) ovarian, primary peritoneal cancer and/or fallopian-tube cancer. All patients should be candidates for cytoreductive surgery which could be conducted as immediate upfront primary surgery following diagnosis or can be conducted after initiation of platinum based neoadjuvant chemotherapy. All patients should be eligible to start first line platinum based chemotherapy in combination with bevacizumab. The study aims to evaluate the efficacy and safety of standard of care (SoC) platinum-based chemotherapy and bevacizumab followed by maintenance bevacizumab either as monotherapy, or in combination with durvalumab, or in combination with durvalumab and olaparib. Therefore, this study aims to see which combination allows patients to live longer without the cancer coming back or getting worse. The study is also looking to see which combination makes patients live longer and how the treatment and the cancer affects their quality of life.

Trial Phase Phase III

Trial Type Treatment

Lead Organization
AstraZeneca Pharmaceuticals LP

  • Primary ID D081RC00001
  • Secondary IDs NCI-2019-00743, 2017-004632-11
  • ID NCT03737643