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Recruiting NCT05851677

Disitamab Vedotin (RC48-ADC) in Breast Cancer

Observational Breast Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Disitamab vedotin.
Who it may be relevant to
Registry conditions: Breast Cancer. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Disitamab Vedotin (RC48-ADC) in Patients With Breast Cancer: a Real-world Study

Overview

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

Interventions

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

Primary outcome measures

  • Progression-Free Survival [Time frame: From the date of starting Disitamab vedotin to the date of first documentation of progression or death (up to approximately 1 years)]
Secondary outcome measures (1)
  • Adverse events [Time frame: From the date of starting Disitamab vedotin to the end of the treatment (up to approximately 1 year)]

Eligibility criteria

Inclusion criteria

  • Histologically confirmed breast cancer;
  • Prior or current use of Disitamab vedotin (RC48-ADC);

Exclusion criteria

  • Participating in clinical trials involving Disitamab vedotin (RC48-ADC) or not.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Renji Hospital, School of Medicine, Shanghai Jiaotong University — Shanghai

Identifiers

NCT: NCT05851677 · LY2023-062-B

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗