Clinical Trials Directory

Trials / Unknown

UnknownNCT05809024

Select the Appropriate Population for Adding CDK4/6i to Neoadjuvant Endocrine Therapy

Select the Appropriate Population for Adding CDK4/6i to Neoadjuvant Endocrine Therapy in High Risk Early HR+/HER2-breast Cancer Based on Molecular Marker

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Yongsheng Wang · Academic / Other
Sex
Female
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Select the appropriate population for adding CDK4/6 inhibitors therapy in high risk early HR+/HER2-breast cancer based on molecular detection

Conditions

Interventions

TypeNameDescription
DRUGletrozoleHormone receptor positive,HER2 negative participants will receive letrozole as neoadjuvant endocrine therapy,if don't work, CDK4/6 Inhibitor was added.

Timeline

Start date
2023-03-01
Primary completion
2025-03-25
Completion
2026-03-25
First posted
2023-04-12
Last updated
2023-04-12

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05809024. Inclusion in this directory is not an endorsement.