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Drug Intensive Monitoring Study of Olaparib in Clinical Practice Among Chinese Patients
Sponsor: AstraZeneca
Summary
This is a multi-centre, prospective, non-interventional study. The study will enrol about 860 Chinese cancer patients from around 56 sites. For OC cohort, the subjects who had received olaparib for at least one dose before study enrolment in real world practices will be enrolled ( n=800) . For PC cohort, according to the doctor's decision, patients who have prescribed and agreed to start taking at least one dose of Olaparib will be enrolled ( n=60). Patient's treating physician is in charge of prescribing (including dose-adjusting or interruption) or discontinuation of olaparib.
Official title: A Multi-Centre, Prospective, Non-Interventional Study to Intensively Monitor the Safety of Olaparib in Clinical Practice Among Chinese Patients.
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
1018
Start Date
2021-03-15
Completion Date
2025-09-05
Last Updated
2026-07-08
Healthy Volunteers
No
Conditions
Locations (37)
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Anhui, China
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Beijing, China
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Changsha, China
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Chengdu, China
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Chongqing, China
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Dongguan, China
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Foshan, China
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Fujian, China
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Guangdong, China
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Guangzhou, China
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Guangzho, China
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Guizhou, China
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Hangzhou, China
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He'nan, China
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Hebei, China
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Heilongjiang, China
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Henan, China
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Huizhou, China
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Jiangsu, China
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Jiangxi, China
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Jilin City, China
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Jinghou, China
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Liaoning, China
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Luzhou, China
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Nanjing, China
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Nantong, China
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Ningbo, China
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Shandong, China
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Shanghai, China
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Shenyang, China
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Sichuan, China
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Taiyuan, China
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Tianjin, China
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Yichang, China
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Yunan, China
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Zhejiang, China
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Zhengzhou, China