Celltrion Secures Three-Year Biologics API Contract, 2027–2029, Expands Global CDMO Footprint
Celltrion announced that it has signed a three-year contract to supply biologics active pharmaceutical ingredients to a global pharmaceutical company from 2027 to 2029. The deal is valued at about 294.9 billion won, with a possible ceiling of up to 375.4 billion won, and production preparations will begin early to ensure a stable supply.
The company said the contract reflects its track record of high-quality production, stable supply capabilities, and efficient manufacturing processes that meet global standards, earning the client’s confidence.
The agreement adds to a rapidly expanding global CDMO business for Celltrion. Earlier this year, it signed a CMO contract with U.S. giant Eli Lilly worth about 678.7 billion won, and as of the first quarter the cumulative backlog for CDMO orders had reached around 1 trillion won.

To support growth, Celltrion is strengthening its global sales and project management capabilities through its subsidiary Celltrion Biosolutions, aiming to coordinate a broader CDMO footprint with clients worldwide.
Beyond traditional manufacturing, the company is pursuing a differentiated formulation CDMO model. It has developed subcutaneous formulation technologies during its RemsimaSC and HerzumaSC programs and is offering these capabilities to external customers as a form-factor CMO service.

Celltrion’s production capacity totals about 316,000 liters, with Songdo in Incheon hosting three plants (about 250,000 liters) and the Branchburg, New Jersey facility contributing about 66,000 liters.
Looking ahead, the group says it is weighing additional capacity expansions both domestically and abroad to meet growing global demand for biologics, while also planning to increase output for its own products, including Jimpentra, as well as new launches.
For U.S. readers, the development highlights how South Korea’s CDMOs are becoming critical nodes in global biologics supply chains. Large U.S. pharmaceutical companies increasingly rely on external manufacturing partners for complex biologics, and ongoing cross-border deals—including Celltrion’s New Jersey presence—illustrate deeper integration between U.S. and Korean biopharma ecosystems. The expansion of formulation and formulation-CDMO services could affect access, pricing, and resilience of biologic therapies in the American market.