Dataset Information

Safety and immunogenicity of the measles vector-based SARS-CoV-2 vaccine candidate, V591, in adults: results from a phase 1/2 randomised, double-blind, placebo-controlled, dose-ranging trial.

ABSTRACT:

Background

We report on the safety and immunogenicity of V591, a measles vector-based SARS-CoV-2 vaccine candidate.

Methods

In this multicentre, randomised, placebo-controlled, double-blind, phase 1/2 trial, healthy adults with no history of COVID-19 disease were assigned to intramuscular injection of V591 or placebo (4:1 ratio). In part 1, younger adults (18-55 years) received V591 median tissue culture infectious dose (TCID₅₀)-levels of 1×10⁵ or 1×10⁶ or placebo, 56 days apart. In part 2, younger and older (>55 years) adults received a single dose of one of four (10⁴/10⁵/10⁶/10⁷) or one of two (10⁵/10⁶) V591 TCID₅₀ levels, respectively, or placebo.

Primary outcome

safety/tolerability. Secondary outcome: humoral immunogenicity. ClinicalTrials.gov: NCT04498247.

Findings

From August-December 2020, 444 participants were screened and 263 randomised (210 V591; 53 placebo); 262 received at least one and 10 received two doses of V591 or placebo. Adverse events were experienced by 140/209 (67.0%) V591 dose-group participants and 37/53 (69.8%) placebo-group participants following injection 1; most frequent were fatigue (57 [27.3%] vs 20 [37.7%]), headache (57 [27.3%] vs 19 [35.8%]), myalgia (35 [16.7%] vs 10 [18.9%]), and injection-site pain (35 [16.7%] vs 4 [7.5%]). No deaths nor vaccine-related serious adverse events occurred. At Day 29, no anti-SARS-CoV-2 spike serum neutralising antibody and IgG-responses were identified in placebo or the three lower V591 dose-groups; responses were detected with V591 1×10⁷ TCID₅₀, although titres were lower than convalescent serum.

Interpretation

V591 was generally well tolerated, but immunogenicity was insufficient to warrant continued development.

Funding

Merck Sharp & Dohme, Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA.

SUBMITTER: Vanhoutte F

PROVIDER: S-EPMC8759950 | biostudies-literature | 2022 Jan

REPOSITORIES: biostudies-literature

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Publications

Safety and immunogenicity of the measles vector-based SARS-CoV-2 vaccine candidate, V591, in adults: results from a phase 1/2 randomised, double-blind, placebo-controlled, dose-ranging trial.

Vanhoutte Frédéric F Liu Wen W Wiedmann Richard T RT Haspeslagh Liesbeth L Cao Xin X Boundy Keith K Aliprantis Antonios A Davila Michelle M Hartzel Jonathan J Li Jianing J McGuire Mac M Ramsauer Katrin K Tomberger Yvonne Y Tschismarov Roland R Brown Deborah D DD Xu Weifeng W Sachs Jeffrey R JR Russell Kevin K Stoch S Aubrey SA Lai Eseng E

EBioMedicine 20220115

<h4>Background</h4>We report on the safety and immunogenicity of V591, a measles vector-based SARS-CoV-2 vaccine candidate.<h4>Methods</h4>In this multicentre, randomised, placebo-controlled, double-blind, phase 1/2 trial, healthy adults with no history of COVID-19 disease were assigned to intramuscular injection of V591 or placebo (4:1 ratio). In part 1, younger adults (18-55 years) received V591 median tissue culture infectious dose (TCID<sub>50</sub>)-levels of 1×10<sup>5</sup> or 1×10<sup>6< ...[more]

PMID: 35042081

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Dataset Information

Safety and immunogenicity of the measles vector-based SARS-CoV-2 vaccine candidate, V591, in adults: results from a phase 1/2 randomised, double-blind, placebo-controlled, dose-ranging trial.

Background

Methods

Primary outcome

Findings

Interpretation

Funding

Publications

Safety and immunogenicity of the measles vector-based SARS-CoV-2 vaccine candidate, V591, in adults: results from a phase 1/2 randomised, double-blind, placebo-controlled, dose-ranging trial.

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