Study identifier:D0817R00010
ClinicalTrials.gov identifier:NCT04553926
EudraCT identifier:N/A
CTIS identifier:N/A
Lynparza tablet (olaparib) Regulatory Post-Marketing Surveillance
ovarian cancer
N/A
No
-
All
600
Observational
19 Years - 150 Years
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Mar 2025 by AstraZeneca
AstraZeneca
-
The objectives of this study are to assess safety and effectiveness of Lynparza tablet (olaparib, hereinafter “the study drug”) in a real world setting in patients who are prescribed with the study drug according to the approved indications in South Korea
Primary Objective: To assess the safety of the study drug for patients prescribed with the study drug under the approved indications in South Korea Secondary Objective: To assess effectiveness of the study drug for patients prescribed with the study drug under the approved indication in South Korea Exploratory Objective: To assess effectiveness of the study drug for ovarian cancer patients diagnosed as Homologous Recombination Deficiency (HRD) positive via locally available validated HRD test and prescribed with the study drug under the approved indication in South Korea
Location
Status
Location
Seoul, Republic of Korea
Status
Withdrawn
Location
Gunpo, Republic of Korea
Status
Recruiting
Location
Yongin, Republic of Korea
Status
Recruiting
Location
Ilsan, Republic of Korea
Status
Recruiting
Location
Seoul, Republic of Korea
Status
Recruiting
Location
Busan, Republic of Korea
Status
Recruiting
Location
Suwon, Republic of Korea
Status
Recruiting
Location
Daejeon, Republic of Korea
Status
Recruiting
Arms | Assigned Interventions |
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