RecruitingNCT07041606
An Observational Study of Molecular profIling of Advanced and aggRessive ENdometrial Cancer and 1-st Line Treatment Approaches in Russian Federation
Multicenter, Observational, Prospective Study of Molecular Profiling in Advanced and Aggressive Endometrial Cancer Patients and 1-st Line Treatment Approaches in Russian Federation
Sponsor
AstraZeneca
Enrollment
500 participants
Start Date
Jun 24, 2025
Study Type
OBSERVATIONAL
Conditions
Summary
Multicenter, observational, prospective study of molecular profiling in advanced and aggressive endometrial cancer patients and 1-st line treatment approaches in Russian Federation
Eligibility
Sex: FEMALEMin Age: 18 Years
Inclusion Criteria6
- Female patients aged ≥ 18 years old;
- Signed ICF, including consent for archival FFPE tumor tissue block testing;
- Newly diagnosed, histologically confirmed, advanced (III-IV stage) EC, with the date of diagnosis of histologically confirmed disease within 4 months before inclusion;
- Endometrioid type G3 or any non-endometrioid histological type of EC (such as serous carcinoma, clear cell carcinoma, mixed carcinoma, undifferentiated and dedifferentiated carcinoma, carcinosarcoma, others);
- The presence of biopsy or postoperative archival FFPE tumor sample (block);
- Availability of source medical documentation.
Exclusion Criteria1
- \. Patients participating in clinical (interventional) studies since the diagnosis of histologically confirmed, advanced EC.
Locations(21)
View Full Details on ClinicalTrials.gov
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NCT07041606
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