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Lizhu Group: The company's V-01 and V-01D-351 provide a better option for sequential strengthening

Published Time:

2022-07-21

Recently, an investor asked Lizhu Group on the interactive platform of the Shanghai Securities News, "In addition to V-01, does the company have any research and development related to the recently widely prevalent Omicron variant? What is the progress? "

  Lizhu Group stated that it has been closely monitoring the global COVID-19 pandemic trend and the prevalence of COVID-19 variants, and is actively conducting research and development of variant vaccines. Relying on Lizhu's mature recombinant protein vaccine development platform, the company has developed a variety of variant vaccines, including Beta, Delta, and Omicron, as well as related bivalent vaccines, and has conducted relevant research on booster/sequential immunization in animals and researchers' clinical trials.

  Recently, research data on the sequential booster vaccination of Lizhu Group's V-01 and bivalent vaccine V-01D-351 were published in the Journal of Clinical Medicine. The results showed that: In terms of immunogenicity, the sequential vaccination of V-01 and the V-01D-351 bivalent vaccine induced a more potent humoral immune response compared to homologous boosting. In terms of safety, the V-01 and V-01D-351 bivalent vaccines showed good safety and tolerability as sequential booster shots, with no or only mild adverse reactions. The V-01 sequential booster regimen also showed good immunogenicity and safety in elderly subjects. The V-01D-351 sequential booster regimen maintained effective immunogenicity against the wild-type strain and produced strong cross-neutralizing ability against Delta and Omicron BA.1. In addition, the immunogenicity of the V-01D-351 bivalent vaccine booster shot was maintained for a considerable period, with neutralizing antibody responses remaining at high levels up to 90 days post-vaccination. The positive results of this study will further promote the R&D process of V-01 and V-01D-351. The two studies provide a reasonable basis for the design of sequential booster vaccination regimens.

 

Source: Xinhua Net