To Compare the Pharmacokinetics and Pharmacodynamics of HR20014, INS068 and INS062 After Single Subcutaneous Injection in Healthy Subjects

Exclusion Criteria

• •1. A history of recurrent or severe drug food allergy, or known or suspected allergy to any component of the study drug;
• •2. Have a history of hypertension;
• •3. Severe systemic infectious diseases within 1 month before screening;
• •4. Patients with a history of lower extremity deep vein thrombosis or high risk of lower extremity deep vein thrombosis;
• •5. Patients with serious diseases of the psychiatric, cardiovascular, respiratory, digestive, endocrine, blood, urogenital and other systems in the past, or existing diseases of the above systems, were judged by the researchers to be unfit to participate in this study;
• •6. Use of prescription drugs (topical eye/nasal drops and creams and occasional antipyretic and analgesic drugs such as acetaminophen within recommended doses are permitted) and over-the-counter drugs, and Chinese herbal medicine (regular vitamins are allowed) within 2 weeks before screening;
• •7. Presence of any abnormal and clinically significant laboratory tests.
• •8. ECG (12-lead electrocardiogram) showed abnormal and clinically significant.
• •9. Those who have participated in any drug clinical trials within 3 months or 5 half-life periods before screening (the elder shall prevail), who participated in clinical trials are defined as random, prior to screening.
• •10. Blood donation within 1 month before screening; Or patients with trauma or major surgical procedures who donated blood or lost blood ≥400 mL in the 3 months prior to screening.
• •11. Women who are pregnant, breastfeeding or planning to conceive, or women of childbearing potential (WOCBP) are reluctant to use appropriate contraception during the trial.
• •12. The investigators determined that other conditions were inappropriate for participation in this clinical trial.