A Study of Lutetium [177Lu]-BL-ARC001 in Patients With Locally Advanced or Metastatic Lung Cancer, Breast Cancer, Head and Neck Squamous Cell Carcinoma and Other Solid Tumors

Exclusion Criteria

• •1. Use of chemotherapy, biological therapy, or immunotherapy within 4 weeks or 5 half-lives prior to the first dose;
• •2. History of severe heart disease;
• •3. Prolonged QT interval, complete left bundle branch block, or third-degree atrioventricular block;
• •4. Active autoimmune or inflammatory diseases;
• •5. Diagnosis of other malignancies within 5 years prior to the first dose;
• •6. Hypertension poorly controlled by two antihypertensive medications;
• •7. History of interstitial lung disease (ILD) requiring hormonal therapy, current ILD, or ≥ Grade 2 radiation pneumonitis;
• •8. Symptoms of active central nervous system metastasis;
• •9. History of allergy to recombinant humanized antibodies or human-mouse chimeric antibodies, or allergy to any excipient component of 177Lu-BL-ARC001;
• •10. Previous organ transplantation or allogeneic hematopoietic stem cell transplantation (Allo-HSCT);
• •11. Cumulative dose of anthracyclines \>360 mg/m² during prior (neo)adjuvant anthracycline therapy;
• •12. Positive human immunodeficiency virus (HIV) antibody, active tuberculosis, active hepatitis B virus infection, or active hepatitis C virus infection;
• •13. Active infection requiring systemic treatment, such as severe pneumonia, bacteremia, sepsis, etc.;
• •14. Participation in another clinical trial within 4 weeks prior to the first dose;
• •15. Pregnant or lactating women;
• •16. Other conditions deemed by the investigator as unsuitable for participation in this clinical trial.