Disitamab Vedotin (RC48-ADC) in Breast Cancer

NCT05851677 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 45

Last updated 2025-09-17

No results posted yet for this study

Summary

To evaluate the efficacy and safety of Disitamab vedotin (RC48-ADC) in patients with breast cancer.

Conditions

Interventions

DRUG

Disitamab vedotin

recommended but not required regimen of 2.0mg/kg, iv, day1, every 2 weeks

Sponsors & Collaborators

  • RenJi Hospital

    lead OTHER

Principal Investigators

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

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-01
Primary Completion
2027-03-31
Completion
2027-08-31

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 NCT05851677 on ClinicalTrials.gov