We're building a better ClinicalTrials.gov. Check it out and tell us what you think!
Try the New Site
We're building a modernized ClinicalTrials.gov! Visit Beta.ClinicalTrials.gov to try the new functionality.
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Durvalumab Treatment in Combination With Chemotherapy and Bevacizumab, Followed by Maintenance Durvalumab, Bevacizumab and Olaparib Treatment in Advanced Ovarian Cancer Patients (DUO-O)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03737643
Recruitment Status : Active, not recruiting
First Posted : November 9, 2018
Last Update Posted : April 21, 2023
Sponsor:
Collaborators:
European Network of Gynaecological Oncological Trial Groups (ENGOT)
GOG Foundation, Inc. (GOG Foundation)
Myriad Genetic Laboratories, Inc.
Information provided by (Responsible Party):
AstraZeneca

Study Description
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
Brief Summary:
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.

Condition or disease Intervention/treatment Phase
Advanced Ovarian Cancer Drug: Bevacizumab Drug: Durvalumab Drug: Olaparib Drug: Placebo olaparib Drug: Durvalumab placebo Drug: Carboplatin+Paclitaxel Phase 3

Detailed Description:

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.

Study Design
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 1404 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: The study consists of 2 independent cohorts: 3 double-blind treatment arms cohort for patients with no tBRCA mutation, and a single open label arm cohort for patients with tBRCA mutation
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Phase III Randomised, Double-Blind, Placebo-Controlled, Multicentre Study of Durvalumab in Combination With Chemotherapy and Bevacizumab, Followed by Maintenance Durvalumab, Bevacizumab and Olaparib in Newly Diagnosed Advanced Ovarian Cancer Patients (DUO-O).
Actual Study Start Date : January 4, 2019
Estimated Primary Completion Date : June 23, 2023
Estimated Study Completion Date : May 25, 2028

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Ovarian Cancer

Arms and Interventions
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Arm Intervention/treatment
Active Comparator: Arm 1
Platinum-based chemotherapy in combination with bevacizumab and durvalumab placebo (saline IV infusion) followed by maintenance bevacizumab, durvalumab placebo (saline IV infusion) and olaparib placebo (tablets).
 Drug: Bevacizumab
Bevacizumab by intravenous infusion. In tBRCAm cohort bevacizumab is optional according to local practice.

Drug: Placebo olaparib
Placebo tablets to match olaparib

Drug: Durvalumab placebo
Matching placebo for intravenous infusion

Drug: Carboplatin+Paclitaxel
Standard of care chemotherapy
Experimental: Arm 2
Platinum-based chemotherapy in combination with bevacizumab and durvalumab followed by maintenance bevacizumab, durvalumab and olaparib placebo.
 Drug: Bevacizumab
Bevacizumab by intravenous infusion. In tBRCAm cohort bevacizumab is optional according to local practice.

Drug: Durvalumab
Durvalumab by intravenous infusion

Drug: Placebo olaparib
Placebo tablets to match olaparib

Drug: Carboplatin+Paclitaxel
Standard of care chemotherapy
Experimental: Arm 3
Platinum-based chemotherapy in combination with bevacizumab and durvalumab followed by maintenance bevacizumab, durvalumab and olaparib.
 Drug: Bevacizumab
Bevacizumab by intravenous infusion. In tBRCAm cohort bevacizumab is optional according to local practice.

Drug: Durvalumab
Durvalumab by intravenous infusion

Drug: Olaparib
Olaparib tablets

Drug: Carboplatin+Paclitaxel
Standard of care chemotherapy
Experimental: tBRCAm cohort
Platinum-based chemotherapy in combination with bevacizumab and durvalumab followed by maintenance bevacizumab, durvalumab and olaparib. Bevacizumab is optional according to local practice.
 Drug: Bevacizumab
Bevacizumab by intravenous infusion. In tBRCAm cohort bevacizumab is optional according to local practice.

Drug: Durvalumab
Durvalumab by intravenous infusion

Drug: Olaparib
Olaparib tablets

Drug: Carboplatin+Paclitaxel
Standard of care chemotherapy


Outcome Measures
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Primary Outcome Measures :
  1. Progression Free Survival (PFS) - in non-tBRCA HRD positive patients [ Time Frame: Approximately 4 years ]
    Defined as time from randomisation to first progression by investigator assessment using modified RECIST 1.1 or death (by any cause in the absence of progression)

  2. Progression Free Survival (PFS) - in all non-tBRCA patients [ Time Frame: Approximately 4 years ]
    Defined as time from randomisation to first progression by investigator assessment using modified RECIST 1.1 or death (by any cause in the absence of progression)


Secondary Outcome Measures :
  1. Progression Free Survival (PFS) - in non-tBRCAm patients [ Time Frame: Approximately 4 years ]
    Defined as time from randomisation to first progression by investigator assessment using modified RECIST 1.1 or death (by any cause in the absence of progression)

  2. Overall Survival (OS) - in non-tBRCA HRD positive patients and in all non-tBRCA patients [ Time Frame: Approximately 7 years ]
    Defined as the time from randomisation to death due to any cause

  3. Second Progression (PFS2) - in non-tBRCAm patients [ Time Frame: Approximately 7 years ]
    Defined as time from randomisation to second progression by investigator assessment of radiological progression, symptomatic progression or death (by any cause in the absence of progression)

  4. Health-related quality of life - in non-tBRCAm patients [ Time Frame: Approximately 4 years ]
    Change from baseline in the physical functioning subscale of the EORTC-QLQ-C30

  5. Pathological Complete Response (pCR) - in non-tBRCAm patients [ Time Frame: Approximately 4 years ]
    Defined as the proportion of patients with pCR in patients undergoing IDS

  6. The pharmacokinetics (PK) and immunogenicity of durvalumab and olaparib as determined by peak concentration - in non-tBRCAm patients [ Time Frame: Approximately 4 years ]
    Determination of durvalumab concentration in serum and olaparib concentration in plasma in a subset of patients

  7. Objective Response Rate (ORR) - in non-tBRCAm patients [ Time Frame: Approximately 4 years ]
    Defined as the number (%) of patients with at least one investigator-assessed visit response of CR or PR as per RECIST 1.1

  8. Duration of response (DoR) - in non-tBRCAm patients [ Time Frame: Approximately 4 years ]
    Defined as the time form the date of first documented response (CR/PR) until the first progression or death in the absence of disease progression

  9. Time to first subsequent therapy (TFST) - in non-tBRCAm patients [ Time Frame: Approximately 7 years ]
    Time elapsed from randomisation to first subsequent therapy or death

  10. Time to second subsequent therapy (TSST) - in non-tBRCAm patients [ Time Frame: Approximately 7 years ]
    Time elapsed from randomisation to second subsequent therapy or death

  11. Time to discontinuation or death (TDT) - in non-tBRCAm patients [ Time Frame: Approximately 4 years ]
    Time elapsed from randomisation to study treatment discontinuation or death

  12. PFS - in tBRCAm patients [ Time Frame: Approximately 4 years ]
    To assess the potential additional clinical benefit of durvalumab added to SoC and olaparib in the first line treatment of tBRCAm patients

  13. PFS2 - in tBRCAm patients [ Time Frame: Approximately 7 years ]
    To assess the potential additional clinical benefit of durvalumab added to SoC and olaparib in the first line treatment of tBRCAm patients

  14. ORR - in tBRCAm patients [ Time Frame: Approximately 4 years ]
    To assess the potential additional clinical benefit of durvalumab added to SoC and olaparib in the first line treatment of tBRCAm patients

  15. ORR pre-surgery in IDS group - in tBRCAm patients [ Time Frame: Approximately 4 years ]
    To assess the potential additional clinical benefit of durvalumab added to SoC and olaparib in the first line treatment of tBRCAm patients

  16. Duration of response (DoR) - in tBRCAm patients [ Time Frame: Approximately 4 years ]
    To assess the potential additional clinical benefit of durvalumab added to SoC and olaparib in the first line treatment of tBRCAm patients

  17. Time to first subsequent therapy (TFST) - in tBRCAm patients [ Time Frame: Approximately 7 years ]
    To assess the potential additional clinical benefit of durvalumab added to SoC and olaparib in the first line treatment of tBRCAm patients

  18. Time to second subsequent therapy (TSST) - in tBRCAm patients [ Time Frame: Approximately 7 years ]
    To assess the potential additional clinical benefit of durvalumab added to SoC and olaparib in the first line treatment of tBRCAm patients

  19. Time to discontinuation or death (TDT) - in tBRCAm patients [ Time Frame: Approximately 4 years ]
    To assess the potential additional clinical benefit of durvalumab added to SoC and olaparib in the first line treatment of tBRCAm patients

  20. Health-related quality of life - in tBRCAm patients [ Time Frame: Approximately 4 years ]
    Change from baseline in the physical functioning subscale of the EORTC-QLQ-C30

  21. Proportion of patients with pCR in patients undergoing IDS - in tBRCAm patients [ Time Frame: Approximately 4 years ]
    To assess the potential additional clinical benefit of durvalumab added to SoC and olaparib in the first line treatment of tBRCAm patients


Other Outcome Measures:
  1. Safety and tolerability of drugs by assessment of AEs/SAEs [ Time Frame: Approximately 4 years ]
    Graded according to the National Cancer Institute (NCI CTCAE)


Eligibility Criteria
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 130 Years   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Gender Based Eligibility:   Yes
Gender Eligibility Description:   All female patients newly diagnosed with advanced ovarian cancer
Accepts Healthy Volunteers:   No
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
Contacts and Locations
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03737643


Locations
Show Show 214 study locations
Sponsors and Collaborators
AstraZeneca
European Network of Gynaecological Oncological Trial Groups (ENGOT)
GOG Foundation, Inc. (GOG Foundation)
Myriad Genetic Laboratories, Inc.
Investigators
Layout table for investigator information
Principal Investigator: Philipp Harter European Network of Gynaecological Oncological Trial Groups (ENGOT)
Principal Investigator: Carol Aghajanian GOG
More Information
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
Layout table for additonal information
Responsible Party: AstraZeneca
ClinicalTrials.gov Identifier: NCT03737643    
Other Study ID Numbers: D081RC00001
2017-004632-11 ( EudraCT Number )
First Posted: November 9, 2018    Key Record Dates
Last Update Posted: April 21, 2023
Last Verified: April 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal. All request will be evaluated as per the AZ disclosure commitment: https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
Supporting Materials: Study Protocol
Statistical Analysis Plan (SAP)
Time Frame: AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA Pharma Data Sharing Principles. For details of our timelines, please rerefer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
Access Criteria: When a request has been approved AstraZeneca will provide access to the de-identified individual patient-level data in an approved sponsored tool . Signed Data Sharing Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information. Additionally, all users will need to accept the terms and conditions of the SAS MSE to gain access. For additional details, please review the Disclosure Statements at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
URL: https://astrazenecagroup-dt.pharmacm.com/DT/Home

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: Yes
Keywords provided by AstraZeneca:
Advanced Ovarian Cancer
Ovarian neoplasms
Additional relevant MeSH terms:
Layout table for MeSH terms
Ovarian Neoplasms
Carcinoma, Ovarian Epithelial
Endocrine Gland Neoplasms
Neoplasms by Site
Neoplasms
Ovarian Diseases
Adnexal Diseases
Genital Diseases, Female
Female Urogenital Diseases
Female Urogenital Diseases and Pregnancy Complications
Urogenital Diseases
Genital Neoplasms, Female
Urogenital Neoplasms
Genital Diseases
Endocrine System Diseases
 Gonadal Disorders
Carcinoma
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Paclitaxel
Bevacizumab
Carboplatin
Durvalumab
Olaparib
Antibodies, Monoclonal
Antineoplastic Agents, Phytogenic
Antineoplastic Agents
Tubulin Modulators
Antimitotic Agents
Mitosis Modulators