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Celltrion expands U.S. operations, boosts drug capacity, and advances oncology pipeline with FDA-reviewed candidates.
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.
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.
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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Celltrion expande las operaciones de los Estados Unidos, aumenta la capacidad de medicamentos y avanza en la tubería de oncología con candidatos revisados por la FDA.