Celltrion Healthcare signs Regkirona deals with 9 European countries

채사라 2021. 11. 30. 16:31
글자크기 설정 파란원을 좌우로 움직이시면 글자크기가 변경 됩니다.

이 글자크기로 변경됩니다.

(예시) 가장 빠른 뉴스가 있고 다양한 정보, 쌍방향 소통이 숨쉬는 다음뉴스를 만나보세요. 다음뉴스는 국내외 주요이슈와 실시간 속보, 문화생활 및 다양한 분야의 뉴스를 입체적으로 전달하고 있습니다.

Celltrion Healthcare has signed agreements with nine European countries for the distribution of Regkirona, Korea's first Covid-19 treatment.
Celltrion's Regkirona Covid-19 treatment [YONHAP]

Celltrion Healthcare has signed agreements with nine European countries for the distribution of Regkirona, Korea's first Covid-19 treatment.

Celltrion Healthcare handles the overseas distribution of biopharmaceuticals developed by Celltrion.

The deals involve 150,000 vials, which can treat 50,000 patients. The distribution could start this year, the company said Tuesday.

Celltion won marketing approval for Regkirona from the European Commission on Nov. 12, only a day after the therapy received an approval recommendation from the Committee for Medicinal Products for Human Use (CHMP) under the European Medicines Agency. Celltrion said it is very rare for the European Commission to grant permission so quickly as it normally takes about one to two months to approve a new drug after the CHMP's recommendation.

"We are currently in talks with another 47 countries," Celltrion Healthcare said in Tuesday's statement. "As the demand for Regkirona is on the rise recently, we anticipate we could win more orders soon."

Around 2.43 million new infections were reported Nov. 15 to 21, up 11 percent compared to the previous week, according to Celltrion Healthcare, citing a report from World Health Organization.

Regkirona received formal marketing authorization from Korea's Ministry of Food and Drug Safety in September. A total of 25,209 patients at 134 hospitals in Korea received the treatment as of Nov. 25.

Staring Nov. 25, Regkirona is being used in regional treatment centers and nursing homes, as well as at government-designated hospitals specializing in infectious diseases. The Korean government expanded the use of Regkirona in an effort to prevent patients with light and moderate symptoms from becoming more seriously ill.

Based on Phase 3 trial results, Regkirona slowed the progression rate of the disease by 70 percent, and by 72 percent for high-risk patients over 50 or those with underlying conditions. Regkirona is administered intravenously for a 60-minute period.

BY SARAH CHEA [chea.sarah@joongang.co.kr]

Copyright © 코리아중앙데일리. 무단전재 및 재배포 금지.

이 기사에 대해 어떻게 생각하시나요?