A triple-blinded randomized control trial to evaluate the safety and immunogenicity of fractional doses of COVID-19 vaccines (ChAd0x1, AD26.COV2. S, and BNT162B2) among Nigeria adults: the SIFCoVAN trial.

A triple-blinded randomized control trial to evaluate the safety and immunogenicity of fractional doses of COVID-19 vaccines (ChAd0x1, AD26.COV2. S, and BNT162B2) among Nigeria adults: the SIFCoVAN trial.

Publication date: Dec 16, 2025

The COVID-19 pandemic posed a major public health challenge with varying devastating effects on the global community. Vaccination is the most effective measure in combating this pandemic. A major challenge, especially in resource-limited settings, was the shortage of the vaccines. However, evidence by WHO in the use of fractionated doses in combating yellow fever prompted the evaluation of the safety and immunogenicity of fractionated doses of COVID-19 vaccines (ChAd0x1, AD26. COV2. S, and BNT162B2) among Nigerian adults (18-65 years). This is a multi-center, non-inferiority randomized, triple-blind trial involving 1812 COVID-19 vaccine nacEFve participants. Six hundred four eligible participants will be randomized into each of the three vaccine arms of ChAd0x1, AD26. COV2. S, and BNT162B2 COVID-19 vaccine. 151 participants will be randomized each into the 25% and 50% fractionated dose and 300 in the standard full dose arm for the ChAd0x1 and AD26. COV2. S group. In the BNT162B2 group, 201 participants will be randomized into the 50% fractionated dose and 403 into the standard dose arms. The efficacy (immunogenicity) will be evaluated by collecting blood samples at baseline (day 0) and day 28 after immunization to determine the geometric mean fold rise (GMFR) of ≥ 2. 5 within the range of 20% non-inferiority to the standard dose of anti-SARS-CoV-2 S antibody response detected by ELISA termed as seroconversion. Safety and adverse events will be evaluated through active evaluation during the first 72 h of vaccine administration and on days 14 and 28 of clinic visits. The trial will also assess secondary immunogenicity variables of 50% plaque plaalite reduction neutralization by antibodies against SARS-CoV-2 variants (α, δ, and _705) and cytokines production (IFNα, γ, and IL-2 producing CD4 and CD8 T lymphocytes). The proposed trial will allow for a comprehensive understanding of the immunologic responses and safety profile of fractional doses compared to full doses of COVID-19 vaccines among Nigerian adults. In addition, this will guide policy implementation for prompt vaccination of the population to maximize access to the limited vaccines available during the COVID-19 pandemic or future epidemics/pandemics. The study is registered at the Pan African Clinical Trials Registry (PACTR), a primary registry in the WHO International Clinical Trial Platforms. PACTR202206754734018. Registered on June 1, 2022, Accessible at: https://pactr. samrc. ac. za/ Trial Sponsor: Open Philanthropy.

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Concepts Keywords
Inferiority Adults
June COVID-19
Pactr202206754734018 Fractional doses
Vaccines Immunogenicity
Nigeria
Safety
Vaccine

Semantics

Type Source Name
disease MESH COVID-19 pandemic
disease MESH yellow fever
pathway REACTOME Reproduction
disease MESH included
drug DRUGBANK Coenzyme M
drug DRUGBANK Deoxy-2-Fluoro-B-D-Cellotrioside
drug DRUGBANK Spinosad
disease MESH plan
disease MESH emergency
disease MESH infection
disease MESH hypersensitivity
drug DRUGBANK Histidine
drug DRUGBANK Magnesium chloride
drug DRUGBANK Ethanol
drug DRUGBANK Sucrose
drug DRUGBANK Sodium Chloride
drug DRUGBANK Cholesterol
drug DRUGBANK Tromethamine
drug DRUGBANK Citric Acid
drug DRUGBANK Polysorbate 80
disease MESH respiratory tract infection
disease MESH gastroenteritis
drug DRUGBANK Oxygen
disease MESH Hepatitis
drug DRUGBANK Etoperidone
disease MESH face
pathway REACTOME Translation
disease MESH pain
disease MESH Infectious Disease
pathway REACTOME Infectious disease
disease MESH Severe Acute Respiratory Syndrome
disease MESH SAO
drug DRUGBANK Medical air
disease MESH BLS
drug DRUGBANK Yellow Fever Vaccine
disease MESH rheumatic diseases
disease MESH Dis

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