Global Vaccine Adjuvant Market: Key Developments
In May 2022, China’s National Medical Products Administration (NMPA) granted approval for GlaxoSmithKline’s (GSK) two-dose vaccine schedule, Cervarix, in girls between the ages of nine to 14 years to prevent cervical cancer. Cervarix is a recombinant, non-infectious, AS04-adjuvanted HPV bivalent (types 16, 18) vaccine.
In July 2021, Dynavax Technologies Corp. and Biological E. Limited (BE) executed a commercial supply agreement of Dynavax’s CpG 1018TM advanced adjuvant for use in BE’s subunit COVID- 19 vaccine candidate, CORBEVAX.
In September 2021, Novavax Inc. enrolled the first participant in its Phase 1/2 study, evaluating the safety and immunogenicity of a combination vaccine using Novavax’s seasonal influenza and COVID-19 vaccine. Clinical trial includes recombinant protein-based NVX-CoV2373 & NanoFlu vaccine candidates and patented saponin-based Matrix-M adjuvant in a single formulation.
In June 2021, Thermo Fisher Scientific entered an agreement with Moderna Inc., a biotechnology company involved in messenger RNA (mRNA) therapeutics and vaccines, for fill/finish sterile manufacturing services and supply packaging for Moderna’s COVID- 19 vaccine.
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