Immunogenicity Study of the Covid-19 (Recombinante) Vaccine - Fiocruz/AstraZeneca When Administered With a 4 or 8 Weeks Interval Between the First Two Doses.
试验速览
- 阶段
- 4 期
- 发起方
- 入组人数
- 1,264
- 试验地点
- 6
- 主要终点
- Geometric mean titers of IgG Anti-S antibody after two doses of Covid-19 (recombinante)
研究概览
简要总结
The purpose of this clinical trial is to compare antibody response and safety of the Covid-19 (recombinante) vaccine according to different time intervals between the first two doses (4, 8 and 12 weeks) and serologic status immediately before the vaccine.
详细描述
After being informed about the study and potential risks, all participants giving written informed consent will be evaluated for eligibility criteria. At day 0, participants who meet the eligibility requirements will undergo a thorough medical evaluation and a urine pregnancy test (if applicable). Eligible participants will be placed in one of three vaccination interval groups (4, 8 or 12 weeks between the first two Covid -19 (recombinante) vaccine doses) in a randomized manner, via a computer program created by the statistical annalist. Both participant and research team will know the allocated group.
Eligible and consenting participants will have a blood sample collected (IgG Anti-S antibodies) and immediately after be administered a third dose of the Covid-19 (recombinante) vaccine. Participants will be instructed to fill out an adverse events journal for solicited adverse events for 7 days and non-solicited adverse events for 28 days after each dose. The research team will contact the participant remotely at least twice during the first two weeks.
The participant will return for a follow-up visit to the research center 28 days after each dose, to evaluate adverse events, collect blood samples (IgG Anti-S antibodies) and undergo a thorough medical evaluation.
The participant will also return to the research center to collect blood samples (IgG Anti-S antibodies) in two more follow-up visits: 6 and 12 months after vaccination with Covid-19 (recombinante).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- None
盲法说明
Only the laboratory technician is blind
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Availability to participate during the entire study, and ability to follow study protocol strictly.
- •Consent to supply personal contact information, such as telephone numbers, address and other information so the research team may contact the participant (For example, in case the participant fails to attend a scheduled visit without previous notice)
- •Ability to understand and sign the volunteered and informed consent form, and ability to fill in the adverse events journal at home, according to the evaluation of the principal investigator ou delegated research team members.
- •Understanding the impossibility of participating in another clinical trial while participating in this clinical trial.
- •Ability to fill out the adverse events journal at home
排除标准
- •Pregnancy or puerperium
- •Having received any other Covid-19 vaccine any time before inclusion in the study
- •Having received any other vaccine 30 days before inclusion in the study
- •Covid-19 disease confirmed by RT-PCR (Real time polymerase chain reaction) up to 28 days before inclusion in the study.
- •Covid-19 symptoms during evaluation of inclusion in the study (Day 0).
- •Fever (Axillary temperature above 37,8 º C / 100,04 °F) 72 hours before vaccination in the study.
- •Contraindications to the Covid-19 (recombinante) vaccine - Fiocruz/AstraZeneca
- •Use of immunosuppressive medication, such as systemic corticosteroids or chemotherapy, or immunosuppressive diseases. We will consider as immunosuppressive doses of systemic corticosteroids daily doses of prednisone of 10mg or more, for more than 14 days.
- •Any discoveries made by the principal investigator that would enhance the risk of an adverse result following the participation in the study, or that in some other way justifies exclusion from the study.
结局指标
主要结局
Geometric mean titers of IgG Anti-S antibody after two doses of Covid-19 (recombinante)
时间窗: 6 months
Geometric mean titers of IgG Anti-S antibodies, obtained immediately before the first dose and 28 days after the second dose of the Covid-19 (recombinante) vaccine, comparing 4 and 8 week intervals to 12 weeks interval between the first two to doses
次要结局
- Geometric mean titer of Anti-S IgG antibodies 6 and 12 months after Covid-19 (recombinante) vaccination(15 months)
- Seroconversion of IgG Anti-S antibodies after two doses of Covid-19 (recombinante) vaccination(6 months)
- Seroconversion of IgG Anti-S antibodies after two doses of Covid-19 (recombinante) by serologic status before vaccination(6 months)
- Reactogenicity and Safety of Covid-19 (recombinante) vaccine(15 months)