Overview
This Phase II/III study assessed the efficacy, safety, pharmacokinetics, and immunogenicity of B013 administered with nab-paclitaxel in participants with locally advanced or metastatic triple negative breast cancer (TNBC) who have not received prior systemic therapy for metastatic breast cancer (mBC).
Eligibility
Inclusion Criteria:
- Women or men aged 18 -75 years
- Locally advanced or metastatic triple negative breast cancer (TNBC)
- No prior chemotherapy or targeted systemic therapy for inoperable locally advanced or metastatic TNBC
- ECOG performance status of 0 or 1
- Patient must have measurable or evaluable disease as defined by RECIST v1.1. Measurable lesions will be confirmed by radiographic imaging (CT or MRI)
Exclusion Criteria:
- Previous treatment is eligible.
- Spinal cord compression not definitively treated with surgery and/or radiation prior to study entry
- Known central nervous system (CNS) disease
- Uncontrolled pleural effusion, pericardial effusion, or ascites Patients
- Uncontrolled tumor-related pain prior to study entry
- The patient has a history of another malignancy within 5 years prior to study entry, except adequately treated non-melanotic skin cancer, carcinoma in situ of the cervix or Papillary carcinoma of the thyroid
- Pregnancy or lactation