- subjects with the lab-confirmed medical history of covid-19, including sars-cov-2 determined by reverse transcription-polymerase chain reaction (rt-pcr) or positive specific antibody igm or igg against serum sars-cov-2. - subjects with the novel onset of pyrexia/cough/shortness of breath/diarrhea or history of contact with confirmed covid-19 individuals within the 14 days before randomization. - pneumonia or active tuberculosis (tb) indicated by chest x-ray, or abnormal and clinically significant as judged by the investigator. - abnormal blood pressure or pulse rate: systolic blood pressure (sbp) ≥ 140 mmhg or diastolic blood pressure (dbp) ≥ 90 mmhg, sbp ≤ 90 mmhg or dbp < 60 mmhg, pulse rate < 50 beats /min or > 100 beats/min at screening and clinically significant as judged by the investigator. - clinically significant 12-lead ecg abnormalities, or qtcf interval > 450 msec at screening, or history of clinically significant ecg abnormalities, which may increase the risk to the subject as judged by the investigator. - use of monoclonal antibodies or fusion proteins within 6 months before screening. - subjects with previous exposure to vaccines in 3 months before screening, or who plans to receive vaccination during the study period or in 3 months after the study. - history of allergy to any monoclonal antibody, fusion protein, biological product, protein product, or ingredient of the ip. - family history of cardiovascular disease, history of atherosclerosis, presence of chronic obstructive pulmonary disease (copd), cirrhosis, cardiovascular disease, or any condition that requires active medical intervention or monitoring to avert serious danger to the participant's health or well-being. - history of blood loss or blood donation (including blood component donation) ≥ 400 ml, or reception of blood transfusion within 3 months prior to screening; blood loss or donation (including blood component donation) ≥ 200 ml within 1 month prior to screening. - previous surgery within 2 months before screening, or scheduled surgery during the study. - previous administration of any investigational drugs/comparators in clinical trials within 3 0 days or remaining in the elimination period of the drug (within 5 half-lives) before screening, or still in the follow-up period of a certain clinical study. - use of prescribed drugs, over-the-counter (otc) drugs, or herbal medicines (excluding vitamins and mineral supplements) within 14 days before screening. - history of alcohol abuse or intake of excessive alcohol in the past 6 months (15 unit of alcohol per week: 1 unit = 285 ml beer, or 25 ml liquor, or 100 ml wine), or alcohol breath test positive, or unwilling/unable to quit alcohol drinking during the study. - subjects who smoke ≥ 5 cigarettes per day or are positive in tobacco screening , or those who are unwilling/unable to quit nicotine intake during the study. - positive for hepatitis b surface antigen (hbsag), hepatitis c virus antibody (anti-hcv), human immunodeficiency virus antibody (anti-hiv) antibody, treponema pallidumparticle agglutination test (tppa) or tuberculosis (tb) quantiferon at screening. - positive β-human chorionic gonadotropin (β-hcg) or breastfeeding female subjects. - history of narcotics abuse or addiction, or positive drug screening. - other conditions unsuitable for participation in the study determined by the investigator, such as potential compliance issues, inability to complete all tests and evaluations required in the protocol, and uncontrolled psychiatric or mental illnesses.

- subjects with the lab-confirmed medical history of covid-19, including sars-cov-2 determined by reverse transcription-polymerase chain reaction (rt-pcr) or positive specific antibody igm or igg against serum sars-cov-2. - subjects with the novel onset of pyrexia/cough/shortness of breath/diarrhea or history of contact with confirmed covid-19 individuals within the 14 days before randomization. - pneumonia or active tuberculosis (tb) indicated by chest x-ray, or abnormal and clinically significant as judged by the investigator. - abnormal blood pressure or pulse rate: systolic blood pressure (sbp) ≥ 140 mmhg or diastolic blood pressure (dbp) ≥ 90 mmhg, sbp ≤ 90 mmhg or dbp < 60 mmhg, pulse rate < 50 beats /min or > 100 beats/min at screening and clinically significant as judged by the investigator. - clinically significant 12-lead ecg abnormalities, or qtcf interval > 450 msec at screening, or history of clinically significant ecg abnormalities, which may increase the risk to the subject as judged by the investigator. - use of monoclonal antibodies or fusion proteins within 6 months before screening. - subjects with previous exposure to vaccines in 3 months before screening, or who plans to receive vaccination during the study period or in 3 months after the study. - history of allergy to any monoclonal antibody, fusion protein, biological product, protein product, or ingredient of the ip. - family history of cardiovascular disease, history of atherosclerosis, presence of chronic obstructive pulmonary disease (copd), cirrhosis, cardiovascular disease, or any condition that requires active medical intervention or monitoring to avert serious danger to the participant's health or well-being. - history of blood loss or blood donation (including blood component donation) ≥ 400 ml, or reception of blood transfusion within 3 months prior to screening; blood loss or donation (including blood component donation) ≥ 200 ml within 1 month prior to screening. - previous surgery within 2 months before screening, or scheduled surgery during the study. - previous administration of any investigational drugs/comparators in clinical trials within 3 0 days or remaining in the elimination period of the drug (within 5 half-lives) before screening, or still in the follow-up period of a certain clinical study. - use of prescribed drugs, over-the-counter (otc) drugs, or herbal medicines (excluding vitamins and mineral supplements) within 14 days before screening. - history of alcohol abuse or intake of excessive alcohol in the past 6 months (15 unit of alcohol per week: 1 unit = 285 ml beer, or 25 ml liquor, or 100 ml wine), or alcohol breath test positive, or unwilling/unable to quit alcohol drinking during the study. - subjects who smoke ≥ 5 cigarettes per day or are positive in tobacco screening , or those who are unwilling/unable to quit nicotine intake during the study. - positive for hepatitis b surface antigen (hbsag), hepatitis c virus antibody (anti-hcv), human immunodeficiency virus antibody (anti-hiv) antibody, treponema pallidumparticle agglutination test (tppa) or tuberculosis (tb) quantiferon at screening. - positive β-human chorionic gonadotropin (β-hcg) or breastfeeding female subjects. - history of narcotics abuse or addiction, or positive drug screening. - other conditions unsuitable for participation in the study determined by the investigator, such as potential compliance issues, inability to complete all tests and evaluations required in the protocol, and uncontrolled psychiatric or mental illnesses.