Phase II/III of Recombinant Human Albumin Injection

Inclusion Criteria: * Male or female subjects aged 18-65 years (inclusive). * Subjects with body weight ≥ 55.0 kg. * Subjects who were diagnosed as liver cirrhosis with ascites according to the Guidelines for Diagnosis and Treatment of Liver Cirrhosis with Ascites and Related Complications (2017) issued by the Chinese Society of Hepatology CMA, with ascites graded 1-2 at diagnosis or after treatment, and also met the requirement of ALB \< 30 g/L (based on test values on Day -14 to Day -3). * Subjects who were able to understand and comply with the study procedures, voluntarily participated this study, and had signed the informed consent form (ICF). Exclusion Criteria: * Subjects with a history of allergies to biological products derived from Escherichia coli, yeast, or Chinese hamster ovary (CHO) cells, or blood products such as HSA. * Subjects with hepatic encephalopathy of West-Haven HE Grade III or higher. * Subjects with uncontrolled infections, such as body temperature \> 37.5°C, white blood cell count \> 9.5 × 10\^9/L, or neutrophil percentage \> 80% (including severe abdominal infection, upper respiratory tract infection, lower respiratory tract infection, urinary system infection, etc.). * Subjects with a history of hepatorenal syndrome (HRS), or serum creatinine (Cr) \> 2 × the upper limit of normal (ULN), or Cr increased by \> 50% duringat screening period; or presence of urine protein 2+ or more. * Subjects with other severe underlying conditions that, in the opinion of the investigator, affected the participation in this study, including but not limited to malignancies (except for liver cancer patients without portal vein or hepatic vein tumor thrombosis), complicated portal vein thrombosis, non-cirrhotic portal hypertension-related ascites, ischemic heart disease, stroke, chronic obstructive pulmonary disease, and Grade III-IV heart failure, and those with gastrointestinal bleeding who had stopped bleeding for less than 14 days after treatment or failed to stop bleeding after endoscopic variceal ligation. * Subjects with organ transplant. * Female subjects of childbearing potential who had a positive serum pregnancy test, or subjects refused to use contraceptive measures during the study. * Subjects who had participated in other clinical trials and received investigational drugs within 3 months prior to screening. * Subjects with abnormal laboratory test values:a.Hematology: platelets (PLT) \< 30 × 10\^9/L, hemoglobin (HGB) \< 70 g/L;b.Alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) \> 5 × ULN, serum total bilirubin (TBIL) \> 3 × ULN;c.Prothrombin activity \< 40%, prothrombin time (PT) prolonged by \> 5 seconds;d.Left ventricular ejection fraction (LVEF) \< 50%. * Subjects who were considered inappropriate for participation in the study by the investigator due to other reasons.