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Lonza Full Year 2025 Financial Report

Lonza reported $7B in revenue for 2025, with its CDMO business driving 70% of growth. Strategic shifts, expanded capacity, and a focus on next-gen therapies like CGT and ADCs position Lonza for continued success in 2026. GuideView2 MIN READFebruary 5, 2026
Lonza Full Year 2025 Financial Report

Lonza Reports $7 Billion Revenue, with M-End Driving 70% of Growth

On January 28, 2026, global CDMO giant Lonza released its full-year 2025 performance results in Zurich. The company reported CDMO business revenue of CHF 6.531 billion (approximately $7.28 billion), marking a 21.7% increase year-on-year when adjusted for constant exchange rates. Core EBITDA surpassed CHF 2.064 billion, with a profit margin of 31.6%, up 1.4 percentage points from 2024.


Strategic "Slimming" and Pure CDMO Focus

In 2025, Lonza pursued a series of strategic initiatives and acquisitions under its "OneLonza" banner. A key move was the company's focus on "slimming down" non-CDMO operations, including the spin-off of its Capsules and Health Ingredients (CHI) business, completing a transformation similar to Samsung Biologics, shifting entirely toward a pure CDMO model.

Lonza also made significant investments to expand production capacity. Between 2020 and 2025, the company allocated CHF 10 billion (approximately $11.1 billion) to further develop its U.S., European, and Asian markets, creating a globally integrated manufacturing network that covers all major demand regions—North America, Europe, and Asia.

In 2025, Lonza continued to invest in future growth across technologies

Additionally, the company made substantial strides in its large-scale projects. These included launching commercial-scale bioconjugation production lines at the Visp facility in Switzerland, large-scale sterile filling lines at the Stein facility in Germany, and advancing cell therapies for diabetes at the Portsmouth site in the U.S. The company's global production capacity for mammalian cells, microbes, and ADCs (antibody-drug conjugates) is now running at 90% utilization, turning Lonza's order backlog into tangible results.


Business Structure Diversification: Three CDMO Platforms Drive Half of Revenue

In its latest business structure, Lonza has consolidated its core CDMO operations into three key platforms, each with clear responsibilities and varying performance.
  • Integrated Biologics emerged as the primary growth driver, contributing 55.9% of sales and 62.4% of EBITDA, with a core growth rate of 32.2%. This platform capitalized on strong demand for mammalian cell culture and drug formulation services, bolstered by the recent acquisition of the Vacaville facility. The U.S. market accounts for over 35% of its mammalian cell CDMO capacity, aligning well with the trend toward regionalized supply chains.

  • Advanced Synthesis represents a high-profit segment, contributing 24.7% of sales but 32.7% of profit, with a 41.8% profit margin, up 5.2 percentage points from the previous year. This growth was driven by rapid expansion in bioconjugates and high-potency APIs (HPAPIs), with scale and operational efficiencies continuing to improve.

  • Specialized Modalities faced short-term challenges from a slowdown in Cell and Gene Therapy (CGT) business, with sales dropping by 3.0%. However, the sector showed signs of recovery in Q2, with microbial and bioscience operations returning to growth. Profit margins in this segment stabilized at 17.0%, supported by cost control measures, with expectations of a rebound in 2026.

2025 with exceptional top-line performance in Advanced Synthesis

End-to-End Focus: From Clinical to Commercialization, North American Capacity Drives Growth

In terms of business mix, preclinical and Phase I projects accounted for approximately 10% of revenue, focusing on early-stage drug development. Phase II projects made up about 20%, bridging early research with later-stage commercialization, while Phase III and commercial production contributed 70% of revenue, providing scalable manufacturing services.

Lonza's ever growing global asset footprint and technology breadth enable anever growing, well-diversified portfolio with low volatility over time

  • Preclinical Stage: Lonza’s technology platforms cover nine areas, including mammalian cells, microbes, CGT, and mRNA, addressing over 90% of innovative clinical pipelines. The company offers early-stage research and discovery services using cutting-edge science and a digital ecosystem.

  • Clinical Stage: Lonza boasts a 99% retention rate for clinical projects (adjusted for clinical failures), with Phase I/II projects growing at 50%, and Phase II/III at 35%. The company’s end-to-end execution capacity ensures seamless transitions from R&D to clinical trials.

  • Production Stage: With a globally leading manufacturing network, Lonza operates multiple sites across North America, Europe, and Asia. Over 35% of its U.S. mammalian CDMO capacity is focused on commercialization, with more than 80 commercial projects delivered annually. Large-scale facilities like Vacaville help increase fermentation capacity to over 450,000 liters, while flexible production capabilities cater to small-scale, pilot, and large-scale manufacturing needs to meet regionalized supply chain demands.


Customer Base and North American Growth

Lonza’s client base includes the world’s top 20 pharmaceutical companies, which contribute over 60% of revenue, while orders from small and mid-sized biotech firms continue to increase. Of the 1,000+ molecules in development, 70% are in late-stage clinical or commercialization phases, with significant value concentrated in the M-end (Manufacturing).

North America remains a key revenue driver for Lonza. Thanks to the U.S. Biodefense and Biotech Safety Act, Lonza successfully secured several overflow orders through its U.S. facilities in Vacaville, Houston, and New Hampshire. In 2025, North America accounted for an increased share of revenue, with new U.S. orders growing by over 25% year-on-year, becoming a critical contributor to Lonza’s 20% revenue growth.

Increasing regionalization favors Lonza with its strong global presence

Looking ahead to 2026, Lonza remains optimistic, projecting an 11-12% growth in its CDMO business (slightly higher than industry peers), with EBITDA margins expected to exceed 32%. To achieve this goal, Lonza plans to allocate about 20% of sales toward next-generation therapies like ADCs and Cell and Gene Therapies (CGTs), while continuing its acquisition strategy to strengthen its technical capabilities.


Strategic Similarities with Samsung Biologics

Lonza’s strategic direction aligns closely with that of Samsung Biologics, both of which transitioned to pure-play CDMO models in the past year. Both companies have built out global manufacturing networks, with a focus on the M-end. Their 2025 financial reports clearly show that continued growth in the M-end is driving their performance. In contrast, WuXi AppTec shines in the R-end (Research), with its advanced technical barriers and expanding R&D projects driving ongoing growth in manufacturing.

As the global CDMO industry shifts from being "industry-intensive" to "technology-intensive," the competition between Lonza and Samsung Biologics is expected to intensify. Meanwhile, WuXi AppTec, with its differentiated competitive strategy in the CRDMO (Contract Research, Development, and Manufacturing Organization) full industry chain, remains a leader in another sector of the market.


References

[1]. https://www.lonza.com/investor-relations/~/media/82814A1852E7470398E0881C6189BC1A