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NCT06227117
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 .