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DOI 10.1016/j.vaccine.2025.127748

Медицинская библиотека · Vaccine · 2025

Safety and immunogenicity of COVAC-2, a Sepivac SWE™ adjuvanted SARS-CoV-2 recombinant protein vaccine in healthy adults; a randomized controlled first-in-human dose-escalation trial.

Hamonic Glenn, Pastural Elodie, Arora Supriya, Lew Jocelyne, Cai Yun, Scruten Erin, Buchanan Rachelle, ElSherif May, Ye Lingyun, Courant Thomas, Ventura Roland A, Collin Nicolas, Daugan Matthieu, Gagnon Luc, Hodgson Paul, van Drunen Little-van den Hurk Sylvia, Falzarano Darryl, Sanche Steve, Halperin Scott A, Langley Joanne M, Gerdts Volker, Racine Trina

СтатьяРандомизированное исследованиеКлиническое исследование I фазыПеревод в очереди

Аннотация

BACKGROUND

This first-in-human dose-escalating, randomized, placebo-controlled, observer-blinded study assessed the safety and immunogenicity of a recombinant protein vaccine (COVAC-2) composed of the S1 subunit of the spike protein of SARS-CoV-2 formulated with the oil-in-water adjuvant Sepivac SWE™.

METHODS

Healthy adults (n = 61) with no known prior exposure to SARS-CoV-2 virus or vaccines were enrolled into one of two cohorts, based on age, 18-54 years old (n = 34, Cohort 1) or 55+ years (n = 27, Cohort 2). Participants in both cohorts were randomized to a two-dose schedule of 25 μg, 50 μg, or 100 μg (cohort 1 only) of COVAC-2 vaccine, or placebo on Days 0 and 28. Safety and immunogenicity data were collected from study Day 0 to 365.

RESULTS

The most common adverse events were injection site pain, generalized muscle aches, and headaches in all dose levels and age groups. Most events were grade 1 and 2 in severity but one participant in the 100 μg dose group reported grade 3 adverse events. S1 subunit-specific humoral binding and neutralizing antibody titres peaked with a geometric mean of 817 IU/mL and 168 IU/mL, respectively, in groups vaccinated with COVAC-2 between study Day 42 and 56 and then decreased in the absence of authorized vaccine administration or infection with SARS-CoV-2. Seroconversion in both 18-54 and 55+ cohorts required two doses of vaccine with 100 % of participants seroconverting by Day 42 in the 18-54 cohort and 88 % of participants by Day 42 in the 55+ cohort. No clear T cell response was detected when measuring IFNγ or IL-5 in peripheral blood mononuclear cells following stimulation with SARS-CoV-2 peptides.

CONCLUSIONS

This Phase 1 trial indicated that COVAC-2 is safe and induces high levels of both antigen-specific binding and neutralizing antibodies by Day 42-56 with levels beginning to wane by Day 120.

Для цитирования: Hamonic Glenn, Pastural Elodie, Arora Supriya, Lew Jocelyne, Cai Yun, Scruten Erin, Buchanan Rachelle, ElSherif May, Ye Lingyun, Courant Thomas, Ventura Roland A, Collin Nicolas, Daugan Matthieu, Gagnon Luc, Hodgson Paul, van Drunen Little-van den Hurk Sylvia, Falzarano Darryl, Sanche Steve, Halperin Scott A, Langley Joanne M, Gerdts Volker, Racine Trina. Safety and immunogenicity of COVAC-2, a Sepivac SWE™ adjuvanted SARS-CoV-2 recombinant protein vaccine in healthy adults; a randomized controlled first-in-human dose-escalation trial.. Vaccine. 2025. DOI: 10.1016/j.vaccine.2025.127748.

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