How is Celltrion Countering Tariff Threats with a New Acquisition?

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How is Celltrion Countering Tariff Threats with a New Acquisition?

Synopsis

Celltrion's latest acquisition of a biopharma plant from Eli Lilly is a strategic move aimed at mitigating the risks posed by potential U.S. tariff increases. This investment not only secures production capabilities but also expands their portfolio of biosimilars and original drugs, confirming Celltrion's commitment to growth in the U.S. market.

Key Takeaways

  • Celltrion's acquisition is aimed at mitigating tariff risks.
  • The deal includes a total investment of 1.4 trillion won.
  • The Branchburg facility is FDA-approved and compliant with cGMP.
  • Celltrion plans to expand its biosimilar portfolio significantly.
  • Local production enhances supply chain resilience.

Seoul, Sep 23 (NationPress) Celltrion, a prominent biopharmaceutical firm from South Korea, announced on Tuesday that its U.S. subsidiary has finalized an agreement to acquire a biopharmaceutical manufacturing facility in the United States. This strategic move is expected to mitigate risks associated with potential U.S. tariff increases.

Celltrion USA will purchase the facility from Eli Lilly for 460 billion won (approximately $330 million) and aims to finalize the transaction by year-end, as detailed in a press release reported by Yonhap news agency.

Celltrion Chairman Seo Jung-jin stated during an online press briefing, “This acquisition provides a foundational strategy to protect against tariff risks, complementing our prior initiatives, such as shipping two years’ worth of inventory to the U.S. and enhancing local contract manufacturing organization (CMO) agreements.”

By establishing a domestic production center, Celltrion has developed a comprehensive supply chain in the U.S., covering all stages of drug manufacturing, from production to commercialization.

The company plans to invest 700 billion won in the facility, which includes the acquisition cost, with an additional 700 billion won earmarked for future expansions.

In July, Celltrion was designated as the preferred bidder for the 37-acre facility located in Branchburg, New Jersey, which also includes an extra 10 acres of undeveloped land intended for future development to address increasing market demands.

This Branchburg facility is a large-scale site approved by the U.S. Food and Drug Administration (FDA) for drug substance manufacturing, compliant with current good manufacturing practice (cGMP) regulations. It has a proven history of producing treatments for cancer and autoimmune disorders, according to Celltrion.

Seo added, “We will continue to manufacture pharmaceuticals for Lilly under a CMO agreement at this facility while also producing Celltrion's products.”

In May, U.S. President Donald Trump enacted an executive order aimed at reducing domestic drug prices by comparing them to those in other nations. This order addresses a system where the U.S. pays substantially more for prescription drugs compared to other advanced economies.

Trump has also indicated that tariffs on pharmaceuticals imported into the U.S. could potentially escalate to 250 percent, the most significant level he has threatened thus far.

Celltrion is actively broadening its global biosimilar portfolio, increasing the number of approved products from six to eleven. The company aims to launch 22 biosimilars by 2030 and 41 by 2033, along with plans to initiate clinical trials for 13 original drugs by 2035.

Currently, the company’s sole original drug, Zymfentra, is marketed in the U.S. for treating autoimmune diseases.

Point of View

The strategic importance of local production in mitigating tariff risks cannot be understated. This move illustrates the company's proactive approach to securing its market position amidst uncertain regulatory environments. As a leading player in the biopharmaceutical sector, Celltrion's expansion efforts reflect a broader trend of localizing production to enhance supply chain resilience, a necessary step in today's global economy.
NationPress
23/09/2025

Frequently Asked Questions

What is the purpose of Celltrion's acquisition?
The acquisition aims to eliminate risks associated with potential U.S. tariff hikes, ensuring a stable production base in the U.S.
How much did Celltrion pay for the facility?
Celltrion acquired the facility from Eli Lilly for 460 billion won, equivalent to about $330 million.
What are Celltrion's future plans for the facility?
Celltrion plans to invest an additional 700 billion won for expansion and aims to enhance its biosimilar portfolio.
What regulatory approvals does the facility have?
The Branchburg facility is FDA-approved and complies with current good manufacturing practice (cGMP) regulations.
How many biosimilars does Celltrion plan to commercialize?
Celltrion aims to commercialize 22 biosimilars by 2030 and 41 by 2033.
Nation Press