A Phase III Study of HS-20093 Injection Combined With Adebrelimab Versus Docetaxel in Previously Treated Patients With Advanced or Metastatic Non-Squamous Non-Small Cell Lung Cancer Without Actionable Genomic Alterations

Prior treatment

• Prior pathological diagnosis of mixed non-small cell lung cancer or any transformed non-small cell lung cancer.
• Prior or ongoing treatment with any of the following:
  • Prior or current treatment targeting B7-H3;
  • Prior or current treatment with topoisomerase I inhibitor agents, including antibody-drug conjugates with topoisomerase I inhibitor payloads, etc.;
  • Prior treatment with docetaxel monotherapy or in combination with other agents.
• Persistent adverse reactions caused by prior treatment.
• Prior occurrence of severe or life-threatening immune-mediated adverse events.

Other illness

• History of other primary malignancies.
• Severe, uncontrolled, or active cardiovascular or cerebrovascular disease.
• Severe or poorly controlled hypertension.
• Severe or poorly controlled diabetes mellitus.
• Clinically significant bleeding symptoms or significant bleeding tendency.
• Severe infection.
• History of severe arterial or venous thromboembolic events.
• Known or suspected interstitial pneumonitis, immune-mediated pneumonitis, or radiation pneumonitis.
• Participants with active or history of autoimmune disease with potential for recurrence.

Lab values

• Presence of any of the following abnormal cardiac findings:
  • Evidence of currently clinically significant important arrhythmia or ECG abnormality;
  • Presence of risk factors causing QT interval prolongation or arrhythmic events.

Other

• Untreated brain metastases; uncontrolled brain metastases; presence of leptomeningeal or brainstem metastases; presence of spinal cord compression (identified by radiographic imaging, regardless of symptoms).

• Age ≥18 years at the time of informed consent form (ICF) signature, either sex.
• Be willing to participate in this clinical trial with understanding of study procedures, ability to provide written informed consent, and commitment to comply with all requirements specified in this clinical trial protocol.
• Previously treated patients with histologically or cytologically confirmed diagnosis of advanced or metastatic non-squamous non-small cell lung cancer (nsq-NSCLC).
• Presence of at least one measurable target lesion.
• Eastern Cooperative Oncology Group performance status (ECOG PS) score of 0 to 1.
• Minimum life expectancy \>12 weeks.
• Adequate organ function.
• Absence of the following active infectious diseases: hepatitis B, hepatitis C, human immunodeficiency virus (HIV) infection, tuberculosis, or syphilis.
• Female participants with negative serum pregnancy test result within 7 days prior to first dose administration, or documentation of no pregnancy risk.