To evaluate the efficacy and safety of SHR-A1811 with or without pertuzumab versus trastuzumab, pertuzumab and docetaxel in HER2-Positive Recurrent or Metastatic Breast Cancer
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
868
SHR-A1811 Injection
SHR-A1811 Injection ; Pertuzumab Injection
Trastuzumab Injection;Pertuzumab Injection ; Docetaxel Injection
The First Affiliated Hospital of Nanjing Medical University
Nanjing, Jiangsu, China
Progression Free Survival by Blinded Independent Central Review
Time frame: from first dose to disease progression, or death, whichever comes first, up to 3 years
Progression Free Survival by investigators
Time frame: from first dose to disease progression, or death, whichever comes first, up to 3 years
Overall Survival
Time frame: from first dose to death, up to 6 years
Objective Response Rate
Time frame: from first dose to disease progression or death, whichever comes first, up to 3 years
Duration of response
Time frame: from first dose to disease progression or death, whichever comes first, up to 3 years
AE
Time frame: from Day1 to 40 or 90 days after last dose
Incidence and severity of serious adverse events (SAE)
Time frame: from Day1 to 40 or 90 days after last dose
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