Neoadjuvant Study of DV in Combination Toripalimab or Sequence Chemotherapy in HR-negative, HER2 Low-expressing Breast Cancer

The purpose of this study is to evaluate the Safety and Efficacy of Neoadjuvant study of DV in combination Toripalimab i or sequence chemotherapy in HR-negative, HER2 low-expressing Breast Cancer

Trial Details

NCT ID
NCT06227117
Phase
PHASE2
Sponsor
RemeGen Co., Ltd.
Status
RECRUITING
Cancer Type
HER2 Positive Breast Cancer
Interventions
  • Disitamab Vedotin Injection (18 weeks)
  • Toripalimab (18weeks)
  • Carboplatin
  • Disitamab Vedotin Injection (12 weeks)
  • Sequential Epirubicin
  • Sequential CTX
Locations (sample)
  • Changsha, Hunan, China|28.19874,112.97087
  • Changsha, Hunan, China|28.19874,112.97087
  • Shanghai, Shanghai Municipality, China|31.22222,121.45806
  • Tianjin, Tianjin Municipality, China|39.14222,117.17667
  • Hangzhou, Zhejiang, China|30.29365,120.16142

Key Eligibility Criteria

  • Voluntarily participate and sign the informed consent form;
  • Ages≥18 years;
  • Invasive breast tumour tissue with low HER2 expression confirmed by the central laboratory, defined as HER2 protein expression of IHC 1+ or IHC 2+ …
  • Tumour hormone receptor (HR)-negative, defined as IHC-stained invasive carcinoma with a proportion of cells positive for both ER and PgR nuclear st…

For full eligibility, visit ClinicalTrials.gov.

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