Clinical Research Directory

Inclusion Criteria: 1. Have fully understood and voluntarily sign the ICF for this study; 2. Age of 18-70 years (inclusive), male or female; 3. Esophageal squamous cell carcinoma confirmed histologically or cytologically 4. Second-line patients with disease progression after only first-line standard therapy（Standard treatment: chemotherapy with platinum plus fluorouracil or taxane combined with immunosuppressive regimen .Progression during adjuvant/neoadjuvant therapy or within 6 months of the last dose is considered a first-line standard treatment failure） 5. At least one measurable lesion according to RECIST 1.1; 6. Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of 0-1; 7. Expected survival is more than 3 months 8. Adequate organ function, defined as: Absolute Neutrophil count (ANC) ≥ 1.5 × 10\^9/L; Platelet count (PLT) ≥ 75× 10\^9/L; Hemoglobin (Hb) ≥ 90 g/L; Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 × upper limit of normal (ULN) (≤ 5.0 × ULN for patients with liver metastases); Serum total bilirubin (TBIL) ≤ 1.5 × ULN; Serum creatinine ≤ 1.5 × ULN and Creatinine clearance (CCr)≥60mL/min; Prothrombin time (PT)、activated partial thromboplastin time (APTT)、international normalized ratio(INR)≤1.5 × ULN; 9. Male and female patients of childbearing age must agree to take effective contraceptive measures during treatment and within 6 months after the last dose of treatment. Exclusion Criteria 1. Patients who have previously received any anti-tumor therapy within 4 weeks prior to the first dose; 2. Patients who have previously received any live attenuated vaccine within 4 weeks before the first use of the study treatment or are expected to received any live attenuated vaccine during the study; 3. Prior systemic treatment with anti-VEGF drugs, irinotecan, or any other topoisomerase I inhibitor 4. LVEF \<50%； 5. BMI≤18.5 kg/m\^2 6. Symptomatic central nervous system (CNS) metastases or meningeal metastases; 7. Patients with other types of malignant tumors within 5 years prior to the screening, except for radically resected, non-recurrent skin basal cell carcinoma, skin squamous cell carcinoma, superficial bladder cancer, cervical cancer in situ, or other carcinoma in situ; 8. Patients with bleeding tendency; active bleeding or a history of heavy bleeding within the past 6 months; 9. Urine protein ≥ ++ and 24 h urine protein \> 1.0g at screening period; 10. Presence of any severe and/or uncontrolled disease before starting treatment; 11. Severe lung disease within 6 months before first dosing ； 12. Any active infection requiring antibiotics or hormones systemic treatment by intravenous infusion within 14 days prior to the first dose; 13. Inability to swallow drugs orally, or presence of clinically significant gastrointestinal disorders