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    Home > Active Ingredient News > Infection > Express 90.4% overall protection, positive phase 3 clinical results of recombinant protein new crown vaccine candidate

    Express 90.4% overall protection, positive phase 3 clinical results of recombinant protein new crown vaccine candidate

    • Last Update: 2021-06-22
    • Source: Internet
    • Author: User
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    ▎ WuXi AppTec content team editor On June 14, 2021, Novavax announced that its recombinant protein-based nanoparticle new crown vaccine candidate NVX-CoV2373 reached the primary endpoint in a pivotal phase 3 clinical trial, with an overall protective efficacy of 90.
    4%
    .

    In addition, its protective efficacy against moderate and severe COVID-19 is 100%, and its effectiveness in high-risk populations is 91%
    .

    Moreover, NVX-CoV2373 also showed good protective effect on the main concern mutant (VoC)/mutant to be observed (VoI)
    .

    NVX-CoV2373 is a recombinant protein candidate vaccine produced using Novavax’s recombinant nanoparticle technology.
    In addition to containing the new coronavirus spike protein (S protein), it also contains Novavax’s proprietary saponin-based Matrix-M adjuvant, which can By stimulating antigen-presenting cells to enter the injection site, the antigen presentation in the local lymph nodes is enhanced, thereby enhancing the immune response and stimulating the production of high levels of neutralizing antibodies
    .

    NVX-CoV2373 can be stored and kept stable at 2°C-8°C
    .

    Image source: PREVENT-19 conducted on Novavax's official website in the United States and Mexico is a randomized, double-blind, placebo-controlled, pivotal phase 3 clinical trial.
    A total of 29,960 adult volunteers over 18 years old were enrolled in a 2:1 Proportion of vaccination or placebo
    .

    77 symptomatic COVID-19 cases were observed in the trial, of which 63 were observed in the placebo group and 14 cases were observed in the NVX-CoV2373 group.
    The converted overall protective efficacy was 90.
    4% (95% CI: 82.
    9, 94.
    6)
    .

    The 10 moderate and 4 severe COVID-19 cases observed in the trial were all in the placebo group, and the effectiveness of the conversion to moderate or severe COVID-19 was 100% (95% CI: 87, 100)
    .

    The effectiveness of NVX-CoV2373 in the "high-risk" population was 91.
    0% (95% CI: 83.
    6, 95.
    0)
    .

    "High-risk" groups are defined as those over 65 years of age, those under 65 who have certain comorbidities or whose living environment is frequently exposed to COVID-19
    .

    ▲NVX-CoV2373 has an overall protective effect of 90.
    4% (picture source: reference [1]) Among 77 COVID-19 patients, 54 patients’ samples can provide new coronavirus genome sequence data
    .

    Sequencing data showed that 65% of the new coronavirus strains that infected these 54 patients belonged to VOC, 17% belonged to VOI, and 19% belonged to other mutant strains
    .

    Exploratory analysis showed that of the 44 patients who were confirmed to be infected by the VoC/VoI mutant through the genome sequence, 38 appeared in the control group and 6 appeared in the vaccine group
    .

    The validity of conversion based on these data was 93.
    2% (95% CI: 83.
    9, 97.
    1)
    .

    ▲The distribution of new coronavirus mutant strains discovered through genome sequencing (picture source: reference [1]) Preliminary safety data of PREVENT-19 show that the vaccine is usually well tolerated, with a small number of serious adverse events, and is in the vaccine group There was a balance between the placebo group and the placebo group
    .

    In assessing the reactogenicity of the first and second vaccines 7 days after vaccination, pain and tenderness at the injection site were the most common local symptoms, usually mild to moderate in severity and less than 3 days in duration
    .

    The most common systemic symptoms are fatigue, headache and muscle pain, lasting less than 2 days
    .

    ▲NVX-CoV2373 safety data (picture source: reference [1]) "PREVENT-19 confirms the reassuring tolerability and safety of NVX-CoV2373
    .

    " said Dr.
    Gregory M.
    Glenn, President of Novavax R&D, " These data show a consistent and high level of effectiveness, reaffirming the vaccine’s ability to prevent COVID-19 in an environment where the new coronavirus continues to evolve
    .

    "Reference: [1] PREVENT-19 Phase 3 TrialData Factsheet.
    Retrieved June 14, 2021, from https://cdn.
    filestackcontent.
    com/fRM9l0gjQmKfUrWRf86M[2] Novavax COVID-19 Vaccine Demonstrates 90% Overall Efficacy and 100% Protection Against Moderate and Severe Disease in PREVENT-19 Phase 3 Trial.
    Retrieved June 14, 2021, from https://novavax.
    reportablenews.
    com/pr/novavax-covid-19-vaccine-19-demonstrates-90-overall-efficacy-and-100-protection-against-moderate-and-severe-disease-in -prevent-19-phase-3-trial Note: This article aims to introduce the progress of medical and health research, not a treatment plan recommendation
    .

    If you need guidance on treatment plans, please go to a regular hospital for treatment
    .

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