LYNPARZA Breast Cancer in the Adjuvant Setting Japan Post-Marketing Surveillance (PMS)
NCT05677308 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 61
Last updated 2026-03-13
Summary
To evaluate the frequency of bone marrow suppression Adverse Drug Reactions (ADRs) in patients with BRCA mutated HER2 negative high recurrent risk breast cancer treated with LYNPARZA for adjuvant treatment in the actual post-marketing use.
Conditions
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Toshimitsu Tokimoto · AstraZeneca KK
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-03-07
- Primary Completion
- 2026-02-18
- Completion
- 2026-02-18
Countries
- Japan
Study Locations
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