Study identifier:D8111R00028
ClinicalTrials.gov identifier:NCT05697705
EudraCT identifier:N/A
CTIS identifier:N/A
Real-world Effectiveness oF the OxfoRd-astrazeneca Covid-19 vaccine as a second bOoster dose in Brazil (REFORCO-BRAZIL)
COVID-19
N/A
No
-
All
188814085
Observational
18 Years - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Nov 2024 by AstraZeneca
AstraZeneca
-
This study will address specific questions concerning the additional protection of the AZ COVID-19 vaccine as a second booster dose in preventing severe COVID-19 outcomes (hospitalisation, ICU admission etc) and will provide data to inform COVID-19 vaccine booster dose recommendations.
In Brazil, second COVID-19 boosters became available to specific risk groups in early 2022. By June 2022, immunocompromised individuals aged 12 years and above, individuals aged 50 years and above, and healthcare workers were eligible for a second booster. The vaccines available for second booster doses in Brazil are produced by AstraZeneca (AZ), Janssen, Pfizer and Sinovac. While several studies have estimated absolute vaccine effectiveness (aVE) or relative vaccine effectiveness (rVE) of second boosters of mRNA COVID-19 vaccines, only a single study has, to date, estimated aVE of AZ vaccine as a second booster dose, and no studies have estimated rVE for AZ vaccine as a second booster dose. As the pandemic progresses, more individuals are choosing to become vaccinated (and boosted) against COVID-19 and thus there is greater need to evaluate the additional protection offered by a second booster dose amongst individuals previously administered a first booster. This is particularly important in the context of waning protection of a first booster dose. The primary objective is to estimate relative vaccine effectiveness (rVE) against COVID-19 hospitalization of the AZ COVID-19 vaccine as a second booster dose relative to a first booster dose only, of any COVID-19 vaccine, administered at least four months ago. This study will also evaluate rVE of other vaccines used in Brazil as a second booster doses. The study will further evaluate rVE of all vaccines (including the AZ-COVID-19 vaccine) as a first booster dose relative to a complete primary series only, of any COVID-19 vaccine administered at least four months ago."
Location
Location
São Paulo, Brazil, 05403-010
Arms | Assigned Interventions |
---|---|
Population A For evaluating second booster doses | Other: ChAdOx1 nCOV-19 vaccine (Vaxzeria) Used as 2nd booster, 1st booster, or primary series Other: BNT162b2 (Pfizer) Used as 2nd booster, 1st booster, or primary series. Other: Ad26.COV2.S (Janssen) Used as 2nd booster, 1st booster, or primary series. Other: CoronaVac (Sinovac) Used as 2nd booster, 1st booster, or primary series. |
Population B For evaluating first booster doses | Other: ChAdOx1 nCOV-19 vaccine (Vaxzeria) Used as 2nd booster, 1st booster, or primary series Other: BNT162b2 (Pfizer) Used as 2nd booster, 1st booster, or primary series. Other: Ad26.COV2.S (Janssen) Used as 2nd booster, 1st booster, or primary series. Other: CoronaVac (Sinovac) Used as 2nd booster, 1st booster, or primary series. |
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