Clinical Trial of SARS-CoV-2 mRNA Vaccine in Chinese People

NCT ID: NCT05352867

Last Updated: 2023-09-06

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 420 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-03-16
• Study Completion Date: 2023-06-21

Brief Summary

Phase Ⅱ Clinical Trial to Evaluate the Safety and Immunogenicity of the New Coronavirus mRNA Vaccine (LVRNA009) in Chinese People Aged 18~59 Years

Conditions

SARS-CoV-2

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: DOUBLE

Study Groups

50μg group

Group Type: EXPERIMENTAL

SARS-CoV-2 (LVRNA009) 50μg group

Intervention Type: BIOLOGICAL

50μg/person

100μg group

Group Type: EXPERIMENTAL

SARS-CoV-2 (LVRNA009) 100μg group

Intervention Type: BIOLOGICAL

100μg/person

Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

0.5ml/person

Interventions

SARS-CoV-2 (LVRNA009) 50μg group

50μg/person

Intervention Type: BIOLOGICAL

SARS-CoV-2 (LVRNA009) 100μg group

100μg/person

Intervention Type: BIOLOGICAL

Placebo

0.5ml/person

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. The age at the time of the first dose of the vaccine is 18-59 years old, and the gender is not limited;

2. The subject has full capacity for civil conduct;

3. Axillary body temperature is less than 37.3 ℃ on the day of enrollment;

4. Subjects have independent judgment ability, can read, understand and complete vaccination diary cards, and they participate voluntarily and sign an informed consent form.

Exclusion Criteria

1. The subject has a history of contact with a person infected with SARS-CoV-2 (positive nucleic acid test) or a person suspected of being infected within 14 days;

2. Have a history of severe allergies to any vaccines, foods, and drugs, such as urticaria, anaphylactic shock, skin eczema, allergic dyspnea, angioedema, etc.;

3. The subject has a history of hypersensitivity to any component of the study vaccine (SARS-CoV-2 mRNA, Dlin-MC3-DMA, cholesterol, distearoylphosphatidylcholine, PEG2000-DMG, phosphate buffer);

4. Have a history of SARS virus infection;

5. Those with a medical history or family history of epileptic convulsions or convulsions, neurological diseases and mental diseases;

6. There is a history of thrombocytopenia or other coagulation disorders diagnosed by the hospital before enrollment;

7. The investigator judges that they are known or suspected to suffer from more serious diseases at the same time, including: respiratory diseases, tuberculosis, acute infection or active chronic disease, liver and kidney disease, cardiovascular disease (cardiopulmonary failure), and drug-uncontrollable hypertension (systolic blood pressure ≥ 160 mmHg, diastolic blood pressure ≥ 100 mmHg), malignant tumor, infection or allergic skin disease, HIV infection (test report can be provided);

8. Congenital malformations, developmental disorders, or chronic diseases (such as Down's syndrome, diabetes, sickle cell anemia or neurological disorders, Guillain-Barré syndrome) determined by the investigator to be unsuitable for participating in this research;

9. Those with known immunological impairment or low function diagnosed by the hospital before enrollment;

10. There is evidence that he is a smoker, alcohol abuser and drug abuser;

11. Positive SARS-CoV-2 nucleic acid test results and/or positive antibody test results before the first dose of vaccination;

12. Female: a person with a positive urine pregnancy test, who is pregnant, breastfeeding, or has a pregnancy plan within 1 year; male: a person whose spouse has a pregnancy plan within 1 year;

13. Any other investigational or unregistered product (drug, biological product, or device) is being used before the first dose of vaccine, or is planned to be used during the study;

14. Those who received immune enhancement or immunosuppressive therapy within 6 months before the first dose of vaccine (continuous oral or infusion for more than 14 days);

15. Has been diagnosed with congenital or acquired immunodeficiency, or suspected of having a systemic disease that may interfere with the conduct or completion of the study, such as: tuberculosis, hepatitis B, hepatitis C, human immunodeficiency virus (HIV); ), syphilis infection, etc.;

16. Those who have received whole blood, plasma and immune globulin treatment within 6 months before the first dose of vaccine;

17. Received other inactivated vaccines within 14 days before the first dose of vaccine, and received live attenuated vaccines within 28 days;

18. Antipyretic, analgesic and anti-allergic drugs are being used within 3 days before enrollment;

19. Subjects who, in the judgment of the investigator, cannot follow the research procedures, abide by the agreement, or plan to permanently relocate from the local area before the end of the study, or plan to leave the local area for a long time during the scheduled visit;

20. The relevant staff members involved in this research or their immediate family members (such as spouses, parents, siblings or children);

21. According to the judgment of the investigator, there are other circumstances that are not suitable for participating in this clinical trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 59 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Hunan Provincial Center for Disease Control and Prevention

OTHER

Sponsor Role: collaborator

AIM Vaccine Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Tao Huang

Role: PRINCIPAL_INVESTIGATOR

Hunan Provincial Center for Disease Control and Prevention

Locations

Outpatient Department of Hunan Provincial Center For Disease Control And Prevention

Changsha, Hunan, China

Xiangtan Center For Disease Control And Prevention

Xiangtan, Hunan, China

Countries

China

Other Identifiers

LVRNA009-Ⅱ-01

Identifier Type: -

Identifier Source: org_study_id