To Evaluate the Efficacy and Safety of Disitamab Vedotin Combined With Toripalimab Sequential Chemotherapy as Neoadjuvant Treatment in Patients With HR-positive, HER2-low Breast Cancer

The purpose of this study is to evaluate the efficacy and safety of Disitamab Vedotin combined with Toripalimab sequential chemotherapy as in patients with HR-positive, HER2-low breast cancer

Trial Details

NCT ID
NCT06389006
Phase
PHASE2
Sponsor
RemeGen Co., Ltd.
Status
RECRUITING
Cancer Type
HER2 Positive Breast Cancer
Interventions
  • Disitamab Vedotin for Injection
  • Toripalimab
  • Epirubicin
  • Cyclophosphamide
Locations (sample)
  • Shanghai, Fudan University Shanghai Cancer Center, China|31.22222,121.45806

Key Eligibility Criteria

  • Voluntarily agree to participate in the study and sign the informed consent;
  • Age ≥18 years old (including the threshold value);
  • Histologically confirmed invasive breast cancer with clinical stage T1c-T2(≥2cm)cN1-2M0 or T3cN0-2M0;
  • As assessed by the research Center, the subjects can tolerate and plan to undergo radical surgery for breast cancer and have not previously receive…

For full eligibility, visit ClinicalTrials.gov.

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