Clinical Research Directory

Inclusion Criteria: 1. Male or female patients aged ≥18 and ≤70 years 2. Histopathologically confirmed advanced recurrent/metastatic malignant solid tumors that have failed second-line therapy with no standard treatment options available (e.g., advanced soft tissue sarcoma, head and neck squamous cell carcinoma, malignant melanoma) 3. ECOG Performance Status score: 0-1 4. Estimated life expectancy ≥3 months 5. At least 28 days since prior chemotherapy, radiotherapy, or surgery 6. At least 6 weeks since prior use of nitrosoureas or mitomycin C 7. Adequate organ function within 14 days prior to enrollment: * Hemoglobin ≥90 g/L (no blood transfusion within 14 days) * Absolute neutrophil count \>1.5×10⁹/L * Platelet count ≥80×10⁹/L * Total bilirubin ≤1.5×ULN * ALT or AST ≤2.5×ULN (≤5×ULN if liver metastases present) * Creatinine clearance ≥60 mL/min (Cockcroft-Gault formula) * Left ventricular ejection fraction (LVEF) ≥50% 8. Signed written informed consent Exclusion Criteria: 1. Participation in another clinical drug trial within 4 weeks 2. Tumor located adjacent to major blood vessels or trachea 3. Poorly controlled cardiac conditions: NYHA class \>2 heart failure, unstable angina, myocardial infarction within 1 year, or clinically significant arrhythmias requiring treatment 4. Pregnant or breastfeeding women 5. Active pulmonary tuberculosis, bacterial or fungal infection (≥Grade 2 per NCI-CTCAE v5.0); HIV infection, active HBV or HCV infection 6. History of psychotropic substance abuse that cannot be discontinued, or mental disorders 7. Active autoimmune disease or history of autoimmune disease (exceptions: vitiligo; childhood asthma in complete remission) 8. Currently receiving immunosuppressive therapy 9. History of drug abuse or known medical, psychological, or social conditions (e.g., alcoholism, drug addiction) 10. Known allergy, hypersensitivity, or intolerance to IL-22BP or any excipient; history of severe allergic reactions to any drug, food, or vaccine 11. Female subjects with pregnancy plans or male subjects whose partners have pregnancy plans from screening through 12 months after the last dose 12. Any serious concomitant disease that, in the investigator's judgment, would jeopardize patient safety or ability to complete the study