Valneva has been granted a patent for their CpG-adjuvanted SARS-CoV-2 vaccine. The vaccine includes an inactivated SARS-CoV-2 whole virus particle, a CpG-containing oligodeoxynucleotide, and an alum adjuvant. It is designed to induce neutralizing antibodies without causing antibody-dependent enhancement of SARS-CoV-2-associated disease. GlobalData’s report on Valneva gives a 360-degree view of the company including its patenting strategy. Buy the report here.
According to GlobalData’s company profile on Valneva, anti-viral antigen-based compositions was a key innovation area identified from patents. Valneva's grant share as of June 2023 was 1%. Grant share is based on the ratio of number of grants to total number of patents.
Cpg-adjuvanted sars-cov-2 vaccine composition inducing neutralizing antibodies
A recently granted patent (Publication Number: US11684669B2) describes a composition for immunization against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus responsible for the COVID-19 pandemic. The composition includes an inactivated SARS-CoV-2 whole virus particle, a CpG-containing oligodeoxynucleotide (CpG-ODN), and an alum adjuvant. The composition is designed to induce the production of neutralizing antibodies against SARS-CoV-2 when administered intramuscularly. Importantly, the composition does not cause antibody-dependent enhancement of SARS-CoV-2-associated disease.
The inactivated SARS-CoV-2 whole virus particle in the composition has an S protein with at least 96% amino acid sequence identity to a specific sequence (SEQ ID NO: 3). The alum adjuvant used is aluminum hydroxide. The ratio of alum to CpG-ODN in the composition ranges from about 1:3 to about 3:1, with a preferred ratio of about 1:2. The alum content in the composition is between about 0.8 to about 1.2 mg/mL, with a preferred content of about 1 mg/mL. The CpG-ODN content in the composition is between about 1.5 to about 2.5 mg/mL, with a preferred content of about 2 mg/mL.
The amount of inactivated SARS-CoV-2 whole virus particles per dose in the composition is between about 0.25 and about 2.5 milli-absorption units×minutes (mAU) as assessed by size exclusion chromatography-high performance liquid chromatography (SEC-HPLC). Alternatively, the amount can be determined as 35 Antigen Units using a SARS-CoV-2 enzyme-linked immunosorbent assay (ELISA) assay.
The patent also describes a kit that includes the SARS-CoV-2 immunogenic composition along with a second immunogenic composition. The second composition can be another SARS-CoV-2 virus immunogenic composition or a composition for immunization against other viruses such as Japanese encephalitis virus, Zika virus, Dengue virus, influenza virus, or Chikungunya virus.
The patent further includes a method for producing the SARS-CoV-2 immunogenic composition. The method involves producing SARS-CoV-2 whole virus particles with the desired S protein sequence, inactivating the particles, and incorporating them into the immunogenic composition along with the CpG-ODN and alum adjuvant.
Overall, this patent provides a detailed description of a composition and method for immunization against SARS-CoV-2, offering potential insights for the development of effective COVID-19 vaccines.
To know more about GlobalData’s detailed insights on Valneva, buy the report here.
Data Insights
From
The gold standard of business intelligence.
Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors.