N-protein vaccine is effective against COVID-19: phase 3, randomized, double-blind, placebo-controlled clinical trial

被引:4
作者
Rabdano, Sevastyan O. [1 ,6 ]
Ruzanova, Ellina A. [1 ]
Vertyachikh, Anastasiya E. [1 ]
Teplykh, Valeriya A. [1 ]
Emelyanova, Alla B. [1 ]
Rudakov, German O. [1 ]
Arakelov, Sergei A. [1 ]
Pletyukhina, Iuliia V. [1 ]
Saveliev, Nikita S. [1 ]
Lukovenko, Anna A. [1 ]
Fakhretdinova, Liliya N. [1 ]
Safi, Ariana S. [1 ]
Zhirenkina, Ekaterina N. [1 ]
Polyakova, Irina N. [1 ]
Belozerova, Natalia S. [1 ]
V. Klykov, Vladislav [1 ]
Savelieva, Arina P. [1 ]
Ekimov, Aleksey A. [1 ]
V. Pokachalov, Konstantin [1 ]
Merkulov, Vadim A. [2 ,3 ]
Yudin, Sergei M. [4 ]
Kruchko, Daria S. [5 ]
Berzin, Igor A. [5 ]
Skvortsova, Veronika I. [5 ]
机构
[1] Fed Med Biol Agcy Russia SPbSRIVS, St Petersburg Sci Res Inst Vaccines Serums, St Petersburg, Russia
[2] IM Sechenov First Moscow State Med Univ, Sechenov Univ, Moscow, Russia
[3] Minist Hlth Russian Federat, Fed State Budgetary Inst, Ctr Evaluat & Control Finished Pharmaceut Prod, Sci Ctr Expert Evaluat Med Prod, Moscow, Russia
[4] Fed Med Biol Agcy, Ctr Strateg Planning FMBA Russia Fed State Budgeta, Ctr Strateg Planning & Management Biomed Hlth Risk, Moscow, Russia
[5] Fed Med & Biol Agcy Russia, Moscow, Russia
[6] 52 Svobody St, St Petersburg 198320, Russia
关键词
COVID-19; Nucleocapsid protein; Vaccine; Phase; 3; Clinical trial; INTERIM ANALYSIS; SARS-COV-2; RESPONSES; EFFICACY; ANTIBODY; SAFETY;
D O I
10.1016/j.jinf.2024.106288
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Despite the success of first-generation COVID-19 vaccines targeting the spike (S) protein, emerging SARS-CoV-2 variants have led to immune escape, reducing the efficacy of these vaccines. Additionally, some individuals are unable to mount an effective immune response to S protein-based vaccines. This has created a need for alternative vaccine strategies that are less susceptible to mutations and capable of providing broad and durable protection. This study aimed to evaluate the efficacy and safety of a novel COVID-19 vaccine based on the full-length recombinant nucleocapsid (N) protein of SARS-CoV-2. Methods: We conducted a prospective, multicenter, randomized, double-blind, placebo-controlled phase 3 clinical trial (NCT05726084) in Russia. Participants (n = 5229) were adults aged 18 years and older, with a BMI of 18.5-30 kg/m(2), and without significant clinical abnormalities. They were randomized in a 2:1 ratio to receive a single intramuscular dose of either the N protein-based vaccine (50 mu g) or placebo. Randomization was done through block randomization, and masking was ensured by providing visually identical formulations of vaccine and placebo. The primary outcome was the incidence of symptomatic COVID-19 confirmed by PCR more than 15 days after vaccination within a 180-day observation period, analyzed on an intention-to-treat basis. Findings: Between May 18, 2023, and August 9, 2023, 5229 participants were randomized, with 3486 receiving the vaccine and 1743 receiving the placebo. Eight cases of PCR-confirmed symptomatic COVID-19 occurred in the vaccine group (0.23%) compared to 27 cases in the placebo group (1.55%), yielding a vaccine efficacy of 85.2% (95% CI: 67.4-93.3; p < 0.0001). Adverse events were mostly mild and included local injection site reactions. There were no vaccine-related serious adverse events. Interpretation: The N protein-based COVID-19 vaccine demonstrated significant efficacy and a favorable safety profile, suggesting it could be a valuable addition to the global vaccination effort, particularly in addressing immune escape variants and offering an alternative for those unable to respond to S protein-based vaccines. These results support the continued development and potential deployment of N protein-based vaccines in the ongoing fight against COVID-19. (c) 2024 The Author(s). Published by Elsevier Ltd on behalf of The British Infection Association. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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