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The Ministry of Food and Drug Safety has initiated a permit review for Corona 19 antibody treatment from Celltrion, a Korean pharmaceutical company. It is the third time in the world that it has requested approval for its use, and the Ministry of Food and Drug Safety plans to complete the review immediately within the next 40 days. Reporter Park Hong-gu about the report. Celltrion has applied for approval of the use of COVID-19 antibody treatments to licensing authorities for the third time in the world after US pharmaceutical companies Lily and Regeneron. This treatment, called “ Rekironaju ”, is a treatment performed by selecting neutralizing antibodies present in the blood of people cured for Corona 19. It is produced in large quantities by the process of growing cells by inserting the neutralizing antibody gene into a host cell capable of mass production. While the existing treatment, remdesivir, inhibits the replication of the infected Corona 19 virus in cells, Rekyrona is a method in which antibody treatments bind to the site that binds to human cells. In this way, even if the virus enters the body, it is impossible to penetrate cells. Rekironaju is expected to be developed as an injection that is given intravenously over approximately 90 minutes to patients with mild to moderate levels of Corona 19. Celltrion conducted a phase 2 clinical trial in 327 corona patients19 in Romania, Spain, and the United States, including Korea. Although the final phase 3 clinical trial of 720 patients remains, the Ministry of Food and Pharmaceutical Safety plans to verify safety and efficacy based on the data presented above. However, even if the drug is released early next year, the role will inevitably be limited, as it will only apply to patients with mild or moderate severity. Experts say there will be limits to reversing the corona epidemic19. This is YTN Park Hong-gu. ※ ‘Your report becomes news’ YTN awaits your valuable report.
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