COVID-19
Conditions
Keywords
covid-19, Vaccine, Children, Coronavac, Vero Cell
Brief summary
To evaluate the efficacy and safety of vaccinating children and adolescents, aged 3 to 17 years, with a two-dose schedule of the inactivated vaccine (Coronavac) against SARS-Cov-2.
Detailed description
Nine hundred sixty (960) participants will be randomized into 2 groups, in a 2:1 ratio, to receive the inactivated Coronavac/Butantan vaccine (VACC, N=640) and a group to receive the immunizing BNT162b2 (Pfizer) (BNTC, N=320). The VACC group will also be compared to a group of adults aged 18 to 49 who received Coronavac (ADU, N=160). The main outcome will be the geometric title of neutralizing antibodies and the secondary outcomes will be the incidence of the number of cases confirmed by RT-PCR, the cellular immune response and frequency of adverse events. Outcomes will be evaluated before the first dose, and 28 and 90 days after the second dose, and followup after 6 and 12 months. The study hypothesis is that the cellular and humoral immune response of children and adolescents is not inferior to the age group 18 to 49 years, who received Coronavac and compared to children vaccinated with the immunizing BNT162b2 (Pfizer) and that the inactivated vaccine presents lower reactogenicity for the age group studied.
Interventions
BIOLOGICALBNT162b2 (Pfizer)
BNT162b2 (Pfizer) vaccine in 2 doses of 0.1 ml or 0.30 ml (according to age group), 4 weeks apart
BIOLOGICALInactivated Coronavac/Butantan vaccine
Inactivated Coronavac/Butantan vaccine in 2 doses of 0.5 ml, 4 weeks apart
Sponsors
Centro de Pesquisas René Rachou
Butantan Institute
Secretaria de Estado da Saúde do Espírito Santo - SESA
Federal University of Espirito Santo
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Masking description
For blinding, the vaccine dose will be prepared by a pharmacist, who will be the only one who will know which immunizer will be administered. Vaccinators, participants and evaluators will not know which immunizer will be given.
Intervention model description
Participants will be randomized into 2 groups, in a 2:1 ratio, to receive the inactivated Coronavac/Butantan vaccine (VACC) and a group to receive the immunizing BNT162b2 (Pfizer) (BNTC). The VACC group will also be compared to a group of adults aged 18 to 49 who received Coronavac (ADU).
Eligibility
Sex/Gender
ALL
Age
3 Years to 49 Years
Healthy volunteers
Yes
Inclusion criteria
* Age between 3 and 17 years old (VACC and BNTC groups) * Age between 18 and 49 years old (ADU group)
Exclusion criteria
* Pregnant teenagers; * History of severe allergic reaction (anaphylaxis, urticaria or angioedema) to any previously administered vaccine; * Have previously received a vaccine against COVID-19; * Personal history of SARS-CoV-2-related Multisystem Inflammatory Syndrome (MIS-C); * Immunosuppressed due to conditions such as inborn error of metabolism, HIV infection, neoplasia or use of immunosuppressive drugs (systemic corticosteroids for more than 14 days or another immunosuppressant).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| intracytoplasmic cytokines | 12 months | The results will be expressed as a positive percentage frequency for a given cell phenotype. |
| T lymphocytes | 12 months | The results will be expressed as a positive percentage frequency for a given cell phenotype. |
| B lymphocytes | 12 months | The results will be expressed as a positive percentage frequency for a given cell phenotype. |
| Viral neutralization assay | 3 months | Neutralizing antibody titers will be expressed by the ability of antibodies to neutralize up to 50% the number of plaques (PRNT50). Title \> 1:50 will be considered positive. |
| Chemiluminescence serological assay for qualitative and quantitative determination of neutralizing antibodies against Spike protein (anti-SARS-Cov-2 anti-IgG-S) | 3 months | Results are expressed in AU/mL and data interpretation will be as follows: \<50 AU/mL = negative; ≥50 U/mL = positive. |
| Serological assay by chemiluminescence for qualitative and quantitative determination of specific IgG antibodies against the nucleocapsid protein of SARS-Cov-2 | 3 months | Results will be expressed as fluorescence intensity or pg/mL. The cutoff is 1.4 and \<1.4 = negative; ≥1.4 = positive. |
| Dosage of systemic soluble factors | 12 months | Chemokines, cytokines and growth factors - biomarkers of humoral and cellular response. Results will be expressed in pg/mL. |
| Antigen-specific stimulation of peripheral blood mononuclear cells in vitro | 2 months | The results will be expressed as a positive percentage frequency for a given cell phenotype. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Adverse events | 6 months | Surveillance of adverse post-vaccine events (PVAE) and adverse events of special interest (EAIE) will be carried out. |
| RT-PCR confirmed cases | 6 months | Cases confirmed by RT-PCR, whose signs/symptoms have started 15 days after the second dose of vaccine, over 6 months after receiving the vaccine. |
Countries
Brazil
Outcome results
None listed