Overview
The aim of the study is to evaluate the efficacy and safety of SKB264 as first-line treatment for patients with unresectable recurrent or metastatic triple-negative breast cancer (TNBC) whose tumors do not express programmed cell death ligand 1 (PD-L1) or in patients with PD-L1 positive tumors who received prior anti-programmed cell death 1 (PD-1)/PD-L1 inhibitor in early setting
Description
This is a randomized, open-label, multicenter, Phase 3 study to evaluate the efficacy and safety of SKB264 versus investigator's choice chemotherapy as first-line treatment for patients with unresectable recurrent or metastatic TNBC whose tumors do not express PD-L1 or in patients with PD-L1 positive tumors who received prior anti-PD-1/PD-L1 inhibitor in early setting.
Eligibility
Key Inclusion Criteria:
- Histologically and/or cytologically confirmed TNBC.
- De novo metastatic or relapsed ≥ 6 months post completion of treatment with curative intent.
- No prior systemic anti-cancer therapy for unresectable recurrent or metastatic disease.
- Participants whose tumours are PD-L1-negative, or participants whose tumors are PD-L1 positive and have relapsed after prior anti-PD-1/PD-L1 inhibitor for early-stage disease.
- At least one measurable lesion per RECIST v1.1.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1 with no worsening within 2 weeks prior to randomization.
- A life expectancy of at least 3 months.
- Eligible for the chemotherapy options listed as investigator's choice chemotherapy (paclitaxel, nab-paclitaxel, capecitabine, eribulin, or carboplatin) as assessed by the investigator.
- Adequate organ and bone marrow function.
Key Exclusion Criteria:
- Active second malignancy.
- Uncontrolled or clinical significant cardiovascular disease.
- History of noninfectious pneumonitis/interstitial lung disease (ILD) that required steroids or has current pneumonitis/ILD.
- Active infection requiring systemic therapy within 2 weeks of randomization.
- Active hepatitis B or hepatitis C virus infection.
- Human immunodeficiency virus (HIV) positive or history of acquired immunodeficiency syndrome (AIDS); known active syphilis infection.
- Known hypersensitivity to SKB264 or its excipients.
- Previously received TROP2-targeted therapy or topoisomerase 1 inhibitors.
- Prior treatment with the same investigator's choice chemotherapy (except taxane).
- Pregnant or lactating women.