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Study to Assess The Efficacy and Safety of a PARP Inhibitor For The Treatment of BRCA-positive Advanced Breast Cancer
Study to Assess The Efficacy and Safety of a PARP Inhibitor For The Treatment of BRCA-positive Advanced Breast Cancer
CompletedPhase 2
Sponsor: AstraZeneca
Conditions: Breast Neoplasms
Interventions: Olaparib
Countries: United States, Australia, Canada, Germany, Israel, Spain, Sweden, United Kingdom
The purpose of the study is to see if the drug KU-0059436 (olaparib) is effective and well tolerated in treating participants with measurable breast cancer gene (BRCA)1- or BRCA2-positive advanced breast cancer and for whom no curative therapeutic option exists.
Eligibility overview
Sex: FEMALE
Age: 18 Years to 130 Years
Healthy volunteers: No
Study type: INTERVENTIONAL
Eligibility criteria
Inclusion Criteria: * Advanced breast cancer with positive BRCA1 or BRCA2 status * Failed at least one prior chemotherapy * In investigators opinion, no curative standard therapy exists * Measurable disease Exclusion Criteria: * Brain metastases * Less than 28 days since last treatment used to treat the disease * Considered a poor medical risk due to a serious uncontrolled disorder
Locations (17)
- West Hollywood, California, United States
- Boston, Massachusetts, United States
- Melbourne, Australia
- Randwick, Australia
- Duarte, CA, Canada
- Cologne, Germany
- Kiel, Germany
- München, Germany
- Tel Aviv, Israel
- Hospitalet deLlobregat, Spain
- Madrid, Spain
- Lund, Sweden
- Cambridge, United Kingdom
- Edinburgh, United Kingdom
- Fulham, United Kingdom
- London, United Kingdom
- Manchester, United Kingdom