Adjuvant CDK4/6 Inhibitor Use in HR+/HER2- Breast Cancer

NCT07180056 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 229

Last updated 2025-11-19

No results posted yet for this study

Summary

To evaluate the efficacy and safety of adjuvant CDK4/6 inhibitors in patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative breast cancer.

Conditions

Interventions

DRUG

CDK4/6 inhibitor

abemaciclib OR ribociclib

Sponsors & Collaborators

  • Wenjin Yin

    lead OTHER

Principal Investigators

  • Wenjin Yin, M.D. · Renji Hospital,School of Medicine, Shanghai Jiaotong University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-28
Primary Completion
2028-02-29
Completion
2033-02-28

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07180056 on ClinicalTrials.gov