Celltrion maps long-term shift toward antibody-based drug platform

2026. 1. 15. 11:06
음성재생 설정 이동 통신망에서 음성 재생 시 데이터 요금이 발생할 수 있습니다. 글자 수 10,000자 초과 시 일부만 음성으로 제공합니다.
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)
Celltrion Inc. has unveiled a mid- to long-term strategy to move beyond biosimilars and become an antibody-based innovative drug platform company.

Speaking on Tuesday, local time, on the main track of the 44th J.P. Morgan Healthcare Conference in San Francisco, Celltrion Chief Executive Officer Seo Jin-seok said the company “has entered a new growth phase of building a true innovative drug platform beyond biosimilars” and aims to establish a robust innovation pipeline by submitting four to five clinical trial applications annually through 2028.

Seo outlined development roadmaps for 16 novel drug candidates, including antibody-drug conjugates, multispecific antibodies, Fc receptor (FcRn) inhibitors, and obesity treatments.

He also detailed plans for next-generation obesity treatment CT-G32, which Celltrion is developing as a quad-agonist, with a clinical trial application targeted for submission in the second half of next year.

Seo said the company is accelerating new drug development through in-house research and development and collaborations with global biotech companies, noting that it achieved 10 open innovation milestones in a single year to strengthen its global partnership network.

Senior Executive Vice President Lee Hyuk-jae presented plans to expand investment in the Branchburg manufacturing facility in New Jersey, which Celltrion acquired last year.

In December, the company purchased the antibody biologics manufacturing facility from Eli Lilly and Co. for $330 million and plans to invest more than $18 billion over the next 10 years to expand the site.

By 2030, Celltrion aims to boost total capacity at the facility to 132,000 liters and add drug product manufacturing lines, completing an end-to-end manufacturing system in the United States.

“The facility is being positioned as a global strategic production hub for biosimilars, innovative therapies, and some contract manufacturing volumes,” Lee said. “It will enhance speed, scale, and resilience across the global supply chain.”

Copyright © 매일경제 & mk.co.kr. 무단 전재, 재배포 및 AI학습 이용 금지