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Study identifier: NCT04269200 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Active Not RecruitingDUO-E

Durvalumab With or Without Olaparib as Maintenance Therapy After First-Line Treatment of Advanced and Recurrent Endometrial Cancer

Condition: Endometrial Neoplasms  ·  Sponsor: AstraZeneca

PhasePhase 3
Planned participants805
Who can joinFemale, 18 Years to 150 Years
Healthy volunteersNoCheck eligibility criteria ↓
Where201 locations · 22 countries

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

A study to assess the efficacy and safety of durvalumab in combination with platinum-based chemotherapy (paclitaxel + carboplatin) followed by maintenance durvalumab with or without olaparib for patients with newly diagnosed advanced or recurrent endometrial cancer.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Age ≥18 years at the time of screening and female. * Histologically confirmed diagnosis of epithelial endometrial carcinoma. All histologies, including carcinosarcomas, will be allowed. Sarcomas will not be allowed. * Patient must have endometrial cancer in one of the following categories: 1. Newly diagnosed Stage III disease (measurable disease per RECIST 1.1 following surgery or diagnostic biopsy), 2. Newly diagnosed Stage IV disease (with or without disease following surgery or diagnostic biopsy) 3. Recurrence of disease (measurable or non-measurable disease per RECIST 1.1) where the potential for cure by surgery alone or in combination is poor. * Naïve to first line systemic anti-cancer treatment. For patients with recurrent disease only, prior systemic anti-cancer treatment is allowed only if it was administered in the adjuvant setting and there is at least 12 months from date of last dose of systemic anti-cancer treatment administered to date of subsequent relapse * FPPE tumor sample must be available for MMR evaluation. * Has Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 within 7 days of starting study treatment. Exclusion Criteria: * History of leptomeningeal carcinomatosis. * Brain metastases or spinal cord compression. * Prior treatment with PARP inhibitors. * Any prior exposure to immune-mediated therapy, including (but not limited to) other anti CTLA-4, anti-PD-1, anti-PD-L1, or anti-programmed-cell-death ligand 2 (anti-PD-L2) antibodies, excluding therapeutic anticancer vaccines.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (201)

Research SiteTucson, Arizona, United States
Research SiteConcord, California, United States
Research SiteLa Jolla, California, United States
Research SiteSan Francisco, California, United States
Research SiteSanta Barbara, California, United States
Research SiteAurora, Colorado, United States
Research SiteFort Lauderdale, Florida, United States
Research SiteTampa, Florida, United States
Research SiteSavannah, Georgia, United States
Research SiteHonolulu, Hawaii, United States
Research SiteArlington Heights, Illinois, United States
Research SiteChicago, Illinois, United States

+ 189 more locations — full list on the registry record.

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

TucsonConcordLa JollaSan Francisco

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