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NCT04560452Completed

Drug Intensive Monitoring Study of Olaparib in Clinical Practice Among Chinese Patients

A Multi-Centre, Prospective, Non-Interventional Study to Intensively Monitor the Safety of Olaparib in Clinical Practice Among Chinese Patients.

Source: ClinicalTrials.gov · Last updated 8 Jul 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Observational
Enrollment
1018 (actual)
First submitted
7 Sept 2020
Start date
15 Mar 2021
Primary completion date
5 Sept 2025
Lead sponsor
AstraZeneca
NCT number
NCT04560452

What you commit to

  • Study type: Observational
  • Participants enrolled: 1018
  • From 15 Mar 2021 to the primary completion date, 5 Sept 2025
  • 37 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • In other ongoing studies, which prohibit any participation in this non-interventional study judged by investigator.

Who the study is looking for

  • Provision of signed and dated written informed consent by the patient or legally acceptable representative prior to any study-specific procedures
  • Patients diagnosed as olaparib approved tumor types in China
  • Eligible for olaparib treatment per the judgement of the treating physician in clinical practice
  • For OC cohort: at least take one tablet of olaparib before enrolment
  • For PC cohort: according to the doctor's decision, have prescribed and agreed to start taking at least one dose of Olaparib

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (37)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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AnhuiChinaUnknown status
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BeijingChinaUnknown status
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ChangshaChinaUnknown status
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ChengduChinaUnknown status
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ChongqingChinaUnknown status
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DongguanChinaUnknown status
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FoshanChinaUnknown status
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FujianChinaUnknown status
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GuangdongChinaUnknown status
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GuangzhoChinaUnknown status
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GuangzhouChinaUnknown status
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GuizhouChinaUnknown status
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HangzhouChinaUnknown status
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HebeiChinaUnknown status
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HeilongjiangChinaUnknown status
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He'nanChinaUnknown status
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HenanChinaUnknown status
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HuizhouChinaUnknown status
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JiangsuChinaUnknown status
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JiangxiChinaUnknown status
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Jilin CityChinaUnknown status
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JinghouChinaUnknown status
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LiaoningChinaUnknown status
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LuzhouChinaUnknown status
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NanjingChinaUnknown status
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NantongChinaUnknown status
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NingboChinaUnknown status
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ShandongChinaUnknown status
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ShanghaiChinaUnknown status
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ShenyangChinaUnknown status
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SichuanChinaUnknown status
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TaiyuanChinaUnknown status
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TianjinChinaUnknown status
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YichangChinaUnknown status
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YunanChinaUnknown status
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ZhejiangChinaUnknown status
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ZhengzhouChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.