Conto alla rovescia del vaccino domestico COVID-19 sul mercato

“Per quanto riguarda i vaccini, ci saranno grandi novità nelle prossime una o due settimane.” Il 4 dicembre, Wang Junzhi, vice capo del gruppo di esperti sui vaccini R&D classe speciale del gruppo di ricerca scientifica e accademico dell'Accademia cinese di ingegneria, ha tenuto un discorso “Vaccino contro la polmonite COVID-19 e progressi nel farmaco R&D” at the 8th World Conference of Integrated Traditional Chinese and Western Medicine, dicendo questo “600 million inactivated vaccines will be approved for marketing within this year”.

It is reported that as of December 2, ci sono 214 COVID-19 vaccines under research worldwide, di cui 51 have entered clinical research and 14 are from China; 14 patients entered stage ⅲ clinical stage, E 6 patients came from China. Tuttavia, ci sono 6 vaccines in Phase III clinical practice in China, E 4 vaccines are inactivated vaccines, which come from Beijing Institute of Biology, Wuhan Institute of Biology, Kexing Zhongwei and Chinese Academy of Medical Sciences. Inoltre, the recombinant protein vaccine from Zhifei Bio has recently entered Phase III clinical research.

What is the safety and effectiveness of the domestic vaccine? “This itself is the result of our country’s accumulated research and development capabilities, technology and experience in the vaccine field for many years, which reflects China’s relatively good technical advantages and institutional advantages in vaccine research and development.” Wang Junzhi said that inactivated vaccines are relatively mature in China, and the technology is relatively good. Inoltre, the main characteristics of inactivated vaccine are closest to the structure of natural virus, so the immune response of human body is stronger and the safety is controllable after application. Inoltre, the inactivated vaccine is stable and can be transported at 2-8 gradi Celsius, so it is convenient to transport in cold chain.

“The whole R&D, production, quality control, safety and effectiveness evaluation standards of inactivated vaccines are relatively mature. We have rich experience and adopt advanced purification technology and quality control technology to make the purity of antigen reach over 95%, which is consistent with the standard of recombinant protein vaccine. ” Wang Junzhi said that after the inactivated vaccine was prepared, it had obtained good safety and immunogenicity results after multi-phase clinical trials.

In Wang Junzhi’s view, for COVID-19 vaccine, no matter what technical route is adopted, the most important thing is to develop a safe, effective and controllable vaccine by combining the characteristics of pathogens and adopting suitable technologies, which is the most important and the only criterion for judgment.