Safety, Tolerability and Immunogenicity of a Recombinant SARS-CoV-2 Vaccine (Sf9 Cell) in Chinese Healthy Population Aged 18 Years and Older: A Phase I, Single-center, Randomized, Placebo-controlled, Double-blind Study
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- COVID-19
- Sponsor
- Jiangsu Province Centers for Disease Control and Prevention
- Enrollment
- 168
- Locations
- 1
- Primary Endpoint
- Occurrence of adverse reactions (AR) within 7 days after each dose of the recombinant SARS-CoV-2 vaccine (Sf9 cell) or placebo.
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
This is a phase I, single-center, randomized, placebo-controlled, double-blind study, to evaluate safety, tolerability and immunogenicity of a recombinant SARS-CoV-2 vaccine (Sf9 cell) in Chinese healthy population aged 18 years and older. After randomization, the trial for each subject will last for approximately 13 months. Screening period is 1 week prior to randomization (Day -7 to Day -1), and each dose of either SARS-CoV-2 vaccine (Sf9 Cell) or placebo will be given intramuscularly (IM) on Day 0 and Day 28 for a two-dose regimen, or on Day 0, Day 14, and Day 28 for a three-dose regimen. Subjects who are ≥18 years old and ≤ 55 years old will be enrolled in adult group, and healthy elderly population who are >55 years old will be enrolled in elderly group. After adult group completes the follow-up 7 days after first vaccination, elderly group will be recruited.
Detailed Description
This is a phase I, single-center, randomized, placebo-controlled, double-blind study, to evaluate safety, tolerability and immunogenicity of a recombinant SARS-CoV-2 vaccine (Sf9 cell) in Chinese healthy population aged 18 years and older. Healthy adults who are ≥18 years old and ≤55 years old will be enrolled in the adult group and healthy elderly population who are \>55 years old will be enrolled in the elderly group. To ensure the enrollment of healthy subjects, screening tests (hematology, biochemistry, and urinalysis) will be performed prior to the vaccination. In each age group, there are three regimen cohort: middle-dose at 0, 28 schedule, high-dose at 0, 28 schedule, and high-dose at 0,14,28 schedule. The subjects in regimen cohort will be randomized to receive vaccines or placebos at a ratio of 3:1. The study will set up an Independent Data Monitoring Committee (IDMC) to conduct overall supervision. The IDMC is required to review the unblinded data when a significant event or risk occurs in the study that might cause the study to be suspended.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Male or female subjects of ≥ 18 years old with body mass index (BMI) ≥ 18.5 and ≤ 30 at the Screening Visit.
- •The subject can provide with informed consent and signs and dates a written informed consent form (ICF) prior to the initiation of any trial procedures.
- •They must be able to understand and follow trial-related instructions.
- •They must be willing and able to comply with planned visits, treatment schedule, laboratory tests and other requirements of the trial.
- •Negative HIV antibody when screening.
- •Axillary temperature ≤ 37.0ºC.
- •Negative in nucleic acid screening of SARS-CoV-
- •Negative in antibodies (IgG and IgM) screening of SARS-CoV-
- •No imaging features of COVID-19 in chest CT.
- •There were no significant abnormalities in blood routine, blood biochemistry, coagulation function and urine routine, or no clinical significance was determined by doctors (including white blood cell count, lymphocyte count, neutrophil count, platelet, hemoglobin, glutamic pyruvic transaminase ALT, glutamic oxaloacetic transaminase AST, total bilirubin, fasting blood glucose, creatinine, prothrombin time, partially activated prothrombin time, urine protein, urine red blood cells).
Exclusion Criteria
- •Exclusion criteria of prime dose:
- •Subjects with a medical or family history of convulsions, epilepsy, encephalopathy, and psychosis.
- •Allergic to any ingredient in the study vaccine, or used to have a serious vaccine allergic reaction.
- •Women who are positive for urine pregnancy test. Women who are pregnant or breastfeeding or planning to be pregnant within 6 months.
- •Have acute febrile diseases or infectious diseases.
- •History of SARS, SARS-CoV-2 or MERS infection.
- •People with serious cardiovascular diseases, such as arrhythmia, conduction block, myocardial infarction, severe hypertension and can not control using drugs.
- •Patients with severe chronic diseases or progressive conditions can not be smoothly controlled, such as asthma, diabetes, and thyroid diseases.
- •Have congenital or acquired angioedema/neuroedema.
- •Had urticaria 1 year before receiving the study vaccine.
Outcomes
Primary Outcomes
Occurrence of adverse reactions (AR) within 7 days after each dose of the recombinant SARS-CoV-2 vaccine (Sf9 cell) or placebo.
Time Frame: 7 days after each dose.
Occurrence of solicited AR in the subjects within 7 days after each dose of recombinant SARS-CoV-2 vaccine (Sf9 cell) or placebo.
Secondary Outcomes
- Occurrence of adverse events (AE) within 7 days after each dose of the recombinant SARS-CoV-2 vaccine (Sf9 cell) or placebo.(7 days after each dose.)
- Occurrence of AE up to Day 28 after prime and boost vaccination.(Day 28 after prime and boost vaccination.)
- The proportion of SAEs up to Day 28 after prime and boost vaccination.(Day 28 after prime and boost vaccination.)
- The proportion of SAEs up to Month 12 after prime and boost vaccination.(The proportion of subjects experiencing SAEs up to Month 12 after prime and boost vaccination.)
- The proportion of abnormal markers of hematology, blood chemistry and urine analysis within 7 days before prime vaccination and at Day 3 after each dose of recombinant SARS-CoV-2 vaccine (Sf9 cell) or placebo.(7 days before prime vaccination and Day 3 after each dose.)
- GMT of anti-RBD specific antibody at Day 7, Day 14, Day 28, Month 3, Month 6, and Month 12 after boost vaccination.(Day 7, Day 14, Day 28, Month 3, Month 6, and Month 12 after boost vaccination.)
- Four-fold increase in anti-RBD specific antibody titers, at Day 7, Day 14, Day 28, Month 3, Month 6, and Month 12 after boost vaccination.(Day 7, Day 14, Day 28, Month 3, Month 6, and Month 12 after boost vaccination.)
- GMFI of anti-RBD specific antibody at Day 7, Day 14, Day 28, Month 3, Month 6, and Month 12 after boost vaccination.(Day 7, Day 14, Day 28, Month 3, Month 6, and Month 12 after boost vaccination.)
- GMT of SARS-CoV-2 neutralizing antibody at Day 7, Day 14, Day 28, Month 3, Month 6, and Month 12 after boost vaccination.(Day 7, Day 14, Day 28, Month 3, Month 6, and Month 12 after boost vaccination.)
- Four-fold increase in SARS-CoV-2 neutralizing antibody titers, at Day 7, Day 14, Day 28, Month 3, Month 6, and Month 12 after boost vaccination.(Day 7, Day 14, Day 28, Month 3, Month 6, and Month 12 after boost vaccination.)
- GMFI of SARS-CoV-2 neutralizing antibody at Day 7, Day 14, Day 28, Month 3, Month 6, and Month 12 after prime and boost vaccination.(Day 7, Day 14, Day 28, Month 3, Month 6, and Month 12 after boost vaccination.)
- Seroconversion rates of IFN-γ stimulated by the overlapping peptide library of S-RBD protein at Day 14, Day 28 after boost vaccination.(Day 14, Day 28 after boost vaccination.)