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CDK4/6 Inhibitors in Patients With Hormone Receptor-positive Advanced Breast Cancer

Shanghai Jiao Tong University logo

Shanghai Jiao Tong University

Status

Enrolling

Conditions

Breast Cancer

Treatments

Drug: CDK4/6 inhibitor

Study type

Observational

Funder types

Other

Identifiers

NCT05795335
KY2022-097-B

Details and patient eligibility

About

This is an ambispective, single-center study to evaluate the survival outcomes, adverse events and predictive biomarkers for CDK4/6 inhibitors in patients with hormone receptor-positive advanced breast cancer.

Enrollment

172 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged ≥18 and older
  • Confirmed diagnosis of hormone receptor-positive breast cancer.
  • Subjects with locoregionally recurrent or metastatic disease not amenable to curative therapy.
  • Subjects have received or plan to receive CDK4/6 inhibitors for advanced disease.
  • ECOG 0-2
  • Adequate organ function

Exclusion criteria

  • Subjects disable to swallow pills.
  • History of immunodeficiency disease

Trial design

172 participants in 1 patient group

Patients have received or plan to receive CDK4/6 inhibitors for advanced disease.
Treatment:
Drug: CDK4/6 inhibitor

Trial contacts and locations

1

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Central trial contact

Ziping Wu, MD; Qi Lu

Data sourced from clinicaltrials.gov

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