Study identifier:D0817R00018
ClinicalTrials.gov identifier:NCT04222465
EudraCT identifier:N/A
CTIS identifier:N/A
Characterizing the cross-sectional approach to investigate the prevalence of tissue BRCA1/2 mutations in newly diagnosed advanced ovarian cancer patients
ovarian neoplasms
N/A
No
-
Female
207
Observational
20 Years +
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Oct 2021 by AstraZeneca
AstraZeneca
-
This is a multi-center, observational study in Japan. Patients with newly diagnosed FIGO stage III - IV advanced OC will be enrolled sequentially. In this study, data of 200 subjects will be collected at approximately 20 sites in Japan. To reduce regional bias of study sites, the number of enrolled patients per site will be capped
Study design:This is a multi-center, observational study in Japan. Patients with newly diagnosed FIGO stage III - IV advanced OC will be enrolled sequentially. In this study, data of 200 subjects will be collected at approximately 20 sites in Japan. To reduce regional bias of study sites, the number of enrolled patients per site will be capped. Study population:Patients with FIGO stage III - IV epithelial ovarian cancer Drug exposure:Not applicable Planned study sites and sample size:The objective number of patients will be 200 from approximately 20 hospitals.
Location
Location
Kitakyushu, Fukuoka, Japan
Location
Kumamoto, Kumamoto, Japan
Location
Yamagata, Yamagata, Japan
Location
Niigata, Niigata, Japan
Location
Tsukuba, Ibaraki, Japan
Location
Toon, Ehime, Japan
Location
Amagasaki, Hyogo, Japan
Location
Sapporo, Hokkaido, Japan
Arms | Assigned Interventions |
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