FDA approves first-ever Korean blood product to enter U.S. market

신하늬 2023. 12. 18. 19:05
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.

The U.S. FDA approved GC Biopharma's blood product Alyglo, making the drug the first domestically developed blood product to enter the U.S. market.
GC Biopharma headquarters in Gyeonggi [GC BIOPHARMA]

GC Biopharma’s blood product won approval from the U.S. Food and Drug Administration (FDA), the pharmaceutical company said Monday.

GC Biopharma’s Alyglo is the eighth FDA-approved drug developed by a Korean company and the first domestically developed blood product to enter the U.S. market.

GC Biopharma plans to market Alyglo in the United States through its American subsidiary, GC Biopharma USA, by the latter half of next year.

Alyglo, an intravenous immune globulin, is a treatment for patients aged 17 and older with primary humoral immunodeficiency, also known as PI, which encompasses a number of different conditions that impact immunity.

The U.S. immune globulin market size was valued at a total of $10.4 billion in 2022, according to the Marketing Research Bureau. The FDA approved Alyglo on Friday, about a month earlier than it was expected to.

The FDA has rejected GC Biopharma twice since 2015, when the company initially submitted a blood product with a lower level of immune globulin than Alyglo's.

The company conducted Phase 3 clinical trials with Alyglo in the United States and Canada in 2020. It applied again for a biological license in July of this year after the FDA conducted a pre-license inspection of North Chungcheong manufacturing facility.

Alyglo is the second domestically developed drug to win FDA approval this year, following Celltrion’s Zymfentra, which was greenlit for the U.S. market in October. Hanmi Pharmaceutical’s Rolontis received FDA approval in 2022.

Samsung Securities Senior Analyst Seo Keun-hee expects Alyglo to generate 15.6 billion won ($12 million) next year, according to a report published Monday. The figure is estimated to reach 233.6 billion by 2028.

“The initial cost may temporarily increase due to expenses spent to purchase blood in the United States and marketing. But since the immune globulin price in the U.S. is about five times higher than in Korea, the cost burden is expected to be quickly alleviated as Alyglo’s sale grows,” said Seo.

BY SHIN HA-NEE [shin.hanee@joongang.co.kr]

Copyright © 코리아중앙데일리. 무단전재 및 재배포 금지.

이 기사에 대해 어떻게 생각하시나요?