Efficacy of T-Dxd in the Treatment of HER2-positive BCBM After Prior Pyrotinib

NCT06135194 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2023-11-18

No results posted yet for this study

Summary

To evaluate the efficacy and safety of T-DXd in the treatment of HER2-positive breast cancer with brain metastases after treatment with pyrotinib

Conditions

Interventions

DRUG

T-DXd

Efficacy and safety of T-DXd in the treatment of HER2-positive breast cancer with brain metastases after treatment with pyrotinib

Sponsors & Collaborators

  • Beijing 302 Hospital

    lead OTHER

Principal Investigators

  • tao wang · Beijing 302 Hospital

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-04-01
Primary Completion
2023-12-30
Completion
2024-06-30

Countries

  • China

Study Locations

More Related Trials

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 NCT06135194 on ClinicalTrials.gov