Tolerability,Safety,Pharmacokinetic Profile and Immunogenicity of a Recombinant Humanized Anti-SARS-CoV-2 Monoclonal Antibody (JS016) for Injection in Chinese Health Subjects

Inclusion Criteria:

1. Male and female subjects aged 18 to 45 years, inclusive;

2. The body weight no less than 50 kg for male subjects and no less than 45 kg for female
subjects. Body mass index (BMI) = weight (kg)/square of height (m2), ranging from
18-28 kg/m2 (including the critical value);

3. Normal or abnormal but clinically insignificant physical examination, vital signs,
laboratory tests and other accessory examinations (chest radiology, abdominal B-mode
ultrasonography, ECG, etc.);

4. No plan of pregnancy and being willing to use effective contraceptive measures for
subject (including partner) from informed consent to 6 months after administration of
investigational product, see Appendix 5 for the specific contraceptive measures;

5. The subjects are able to understand the content of the study and voluntary to sign the
informed consent form; meanwhile, being able to complete the study as required in the
protocol.

Exclusion Criteria:

Excluded for novel coronavirus (SARS-CoV-2) infection

1. Having one of the following evidence on SARS-CoV-2 infection:

1. SARS-CoV-2 determined by reverse transcription-polymerase chain reaction (RT-PCR)
and/or next generation sequencing (NGS) in diagnostic specimens (nasopharyngeal
swabs) during screening and pre-randomization (results within 3 days before
randomization are accepted);

2. Previous viral gene sequencing showed high homology with the known SARS-CoV-2;

3. Positive specific antibody IgM or IgG against serum SARS-CoV-2; Excluded for
previous and concomitant medications

2. Previous vaccination of SARS-CoV-2 vaccine or having participated in the clinical
trial on SARS-CoV-2 neutralizing antibody;

3. Use of therapeutic biologics within 12 weeks prior to screening, or remaining in the
elimination period of the drug (within 5 half-lives) at random administration,
whichever is longer;

4. Participation in any other clinical study with intervention of investigational product
within 4 weeks prior to screening, or remaining in the elimination period of the drug
(within 5 half-lives) prior to screening, whichever is longer;

5. Vaccination of vaccine within 12 weeks prior to screening, or plan to use Bacille
Calmette-Guérin vaccine or other vaccine during the study and within 12 weeks after
the study;

6. Use of hydroxychloroquine, herbal medicine, any prescription drug or over-the-counter
drug within (inclusive) 14 days prior to screening; Surgery

7. Any major surgery within 8 weeks (inclusive) prior to screening, or requiring such
surgery during the study, and such surgery is considered by the investigator to
possibly bring unacceptable risk for subjects upon confirmation with the sponsor;
Abnormal physical examination, laboratory examination and history

8. Lying systolic blood pressure (SBP) > 140 mmHg or < 90 mmHg, and/or diastolic blood
pressure (DBP) > 90 mmHg or < 50 mmHg at screening and randomization;

9. Total white blood cell (WBC) count < 3.5 x 109/L, platelet < 140 x 109/L, neutrophil <
2.0 x 109/L, or hemoglobin decreased (male < 135 g/L, female < 120 g/L), lymphocytes <
1.0 x 109/L at screening;

10. ALT or AST > 2 × upper limit of normal, or eGFR ≤ 90 mL/min/1.73m2 at screening;

11. Abnormal ECG at screening, single QTcF > 450 msec, and/or other abnormalities of
clinical significance, unacceptable risk that may be brought by participation in the
study;

12. History of HIV infection, and/or positive aiti-HIV antibody, positive hepatitis B
surface antigen (HBsAg), positive hepatitis C antibody (anti-HCV), or
positivetreponema pallidum particle agglutination test (TPPA) at screening;

13. History of transplantation of vital organs (e.g., heart, lung, liver, kidney, etc.);

14. Having malignant tumor (excluding the malignant tumor cured with no recurrence in the
past 5 years, completely resected basal cell and squamous cell carcinoma of skin,
completely resected carcinoma in situ of any type);

15. Other major diseases within one year;

16. Medical history and previous history suggest the following diseases: including but not
limited to gastrointestinal, renal, hepatic, neurological, hematological, endocrine,
oncological, pulmonary, immune, mental or cerebro- and cardiovascular diseases;
Substance abuse, alcohol abuse

17. History of drug abuse or use of narcotics in the past 5 years, or positive urine drug
screening;

18. History of alcohol abuse or intake of excessive alcohol in the past 6 months (14 units
of alcohol per week: 1 unit = 285 mL beer, or 25 mL liquor, or 100 mL wine), or
alcohol test positive; History of allergies

19. Known serious allergic reaction or hypersensitive to food, inhaled and contact
material as well as drugs, or allergic constitution (allergy to various drugs and
food);

20. Known history of allergy or hypersensitivity to the investigational drug, other
monoclonal antibody drugs and therapeutic protein preparations (fresh or frozen
plasma, human serum albumin, cytokine, interleukin etc.); Pregnancy, lactation

21. Positive β-Human Chorionic Gonadotropin (β-HCG) or breastfeeding female subjects;
Blood loss and others

22. Subjects who lost blood or donated more than 400 mL, or received blood transfusion in
the past 3 months; or plan to donate blood during the study;

23. Any other condition that the subject is considered by the investigator as
inappropriate to participate in the study, for example, potential compliance issue,
inability to complete all the tests and evaluations according to the requirements in
the protocol, or uncontrolled mental, neurological or psychological disorders,
participation in the study is judged by the investigator to be associated with
uncontrollable risk.