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Study identifier: NCT07531693 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Patient Relevant Outcomes Improvement Program in High Risk Hormone Receptor Positive (HR+) Breast Cancer

Condition: HR+/HER2- Early Breast Cancer  ·  Sponsor: Institut fuer Frauengesundheit

PhaseN/A
Planned participants200
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this observational study is to evaluate how persistently patients with high-risk early breast cancer take abemaciclib 6 months after therapy start. To this end, researchers will perform a retrospective analysis of therapy data.

This description comes directly from the study's public registry record.

Talk to the study team

Sponsor's study office  ·  +49 15739466438  ·  studien@ifg-erlangen.de

Always discuss trial participation with your own doctor first.

Locations (1)

Department of Obstetrics and Gynaecology, Uniklinikum ErlangenErlangen, Bavaria, GermanyRecruiting

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Source record: clinicaltrials.gov/study/NCT07531693