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flag Celltrion expands U.S. operations, boosts drug capacity, and advances oncology pipeline with FDA-reviewed candidates.

flag Celltrion announced plans to expand its U.S. manufacturing and R&D presence, including acquiring an Eli Lilly facility in New Jersey to add 66,000L of drug substance capacity, with future expansion to 132,000L by 2030. flag The company revealed progress on its innovative drug pipeline, with three antibody-drug conjugate candidates in FDA review, one receiving Fast Track designation for lung cancer. flag Celltrion expects up to 16 new drug applications by 2028, including 10 ADCs and 4 multi-specific antibodies, and aims to commercialize 18 biosimilars by 2030 and 41 by 2038, shifting toward oncology-focused innovation.

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