A Phase II Study of SKB571 in Patients With Lung Cancer

Prior treatment

• Subjects with other malignant tumors within 3 years prior to the first dose.
• Subjects with major surgery within 28 days prior to the first dose.
• Subjects who have received live vaccines within 30 days prior to the first dose of study treatment, or who are scheduled to receive live vaccines during the study.
• Subjects who have received strong cytochrome P450 (CYP3A4) inhibitors or inducers, or BCRP inhibitors within 2 weeks prior to the first dose of study treatment or within 5 half-lives of known drug, whichever is longer.
• Subjects who have received chemotherapy, immunotherapy, or biological therapy within 4 weeks prior to the first dose of study treatment.
• Subjects with active infection requiring systemic anti-infective therapy within 14 days prior to the first dose of study treatment.
• Subjects with any disease requiring systemic treatment with corticosteroids (prednisone at doses \> 10 mg/d or similar drugs with equivalent doses) or other immunosuppressive therapy within 14 days prior to the first dose of study treatment.

Other illness

• Subjects with history of major cardiovascular, cerebrovascular, or thromboembolic disease.
• Subjects with human immunodeficiency virus (HIV) infection, or any known active viral hepatitis, or hepatitis B or hepatitis C.
• Subjects with known allergy or hypersensitivity to SKB571 or its excipients.
• History of noninfectious pneumonitis/interstitial lung disease (ILD) that required steroids or has current pneumonitis/ILD
• Any condition that, in the opinion of the investigator, will interfere with the assessment of study treatment or the safety of the subject or the interpretation of the study results.

Other

• Subjects with known active or untreated central nervous system (CNS) metastases.
• Uncontrolled pleural effusion, pericardial effusion, or ascites effusion requiring repeated drainage.
• Subjects with clinically severe lung injuries due to pulmonary complications.

• Subjects aged 18-75 years at the time of signing the informed consent form
• Subjects with histologically or cytologically confirmed locally advanced or metastatic NSCLC .
• Subjects with at least one measurable lesion assessed by the investigator according to RECIST v1.1.
• Subjects with Eastern Cooperative Oncology Group (ECOG) status score of 0 or 1.
• Subjects who are assessed by the investigator to have an expected survival of ≥ 12 weeks.
• Subjects who have adequate organ function.
• Subjects who have recovered from all toxicities due to prior therapy .
• Male and female subjects must agree to use highly effective contraception methods during the study treatment.
• Subjects who voluntarily sign the informed consent form.