Stock Markets March 26, 2026

Oxford BioMedica Posts 33% Revenue Gain in 2025, Projects Stronger 2026 After U.S. Facility Purchase

Lentiviral manufacturing expansion and service growth lift top line; company flags second-half weighted 2026 performance as Durham site ramps

By Sofia Navarro
Oxford BioMedica Posts 33% Revenue Gain in 2025, Projects Stronger 2026 After U.S. Facility Purchase

Oxford BioMedica reported preliminary 2025 revenue of £168.70 million, up 33% year-on-year and ahead of a consensus £166.22 million from eight analysts. The company delivered positive operating EBITDA of £2.30 million despite a full-year operating loss of £22.50 million. Revenue gains were driven by increased GMP lentiviral vector manufacturing, rising development fees and expanded procurement and storage services, and the firm acquired an FDA-approved viral vector facility in Durham, North Carolina. Management expects 2026 revenue of £220-240 million with an operating EBITDA margin near 10%, noting that next year's results will be weighted to the second half as technology transfers and the Durham ramp-up proceed. Medium-term forecasts call for 25-30% revenue growth in 2027-28 and at least a 20% EBITDA margin in 2027.

Key Points

  • Oxford BioMedica posted preliminary 2025 revenue of £168.70 million, a 33% increase and ahead of a consensus £166.22 million from eight analysts.
  • The company achieved positive operating EBITDA of £2.30 million in 2025, while recording a full-year operating loss of £22.50 million.
  • Oxford BioMedica acquired an FDA-approved viral vector facility in Durham, North Carolina, and forecasts 2026 revenue of £220-240 million with an operating EBITDA margin near 10%, second-half weighted.

Overview

Oxford BioMedica has released preliminary 2025 results showing revenue of £168.70 million, a 33% increase on the prior year and slightly above the consensus estimate of £166.22 million from eight analysts. The UK cell and gene therapy contract development and manufacturing organisation recorded a positive operating EBITDA of £2.30 million for the period, although it reported an operating loss for the year of £22.50 million.

Drivers of 2025 performance

Management attributed the top-line improvement to increased GMP lentiviral vector manufacturing to support both clinical programmes and commercial launch activities. Development revenues rose as clients advanced through clinical development stages, requiring additional work on process characterisation and validation. The company also experienced expansion in procurement and storage services as customers positioned themselves for commercialisation and sought stability in raw material supply chains.

Expansion of U.S. capacity

In 2025 Oxford BioMedica acquired an FDA-approved viral vector facility in Durham, North Carolina, a move that increases its U.S. manufacturing footprint. The company has signalled that this acquisition will be a factor in next year’s operational profile as the site is integrated and scaled.

Outlook for 2026 and beyond

Oxford BioMedica expects 2026 revenue to fall between £220 million and £240 million, with an operating EBITDA margin of approximately 10%. The company cautioned that both revenue and EBITDA will be second-half weighted in 2026 due to ongoing technology transfers and the ramp-up of the Durham facility. Looking further ahead, management projects medium-term revenue growth of 25% to 30% for 2027-28 and an EBITDA margin of at least 20% in 2027.


Context for markets and sectors

The results and guidance touch several areas of the economy and markets, including contract manufacturing services within the biotech sector, supply chain and procurement services for biologics, and the U.S. biomanufacturing landscape where the Durham facility will operate.

Conclusion

Oxford BioMedica closed 2025 with materially improved revenue and moved to a positive operating EBITDA position despite a full-year operating loss. The company’s purchase of an FDA-approved Durham facility and its guidance for material revenue growth and margin improvement in 2026 and beyond set expectations for a back-loaded 2026 as technology transfers and site ramp-up progress.

Risks

  • 2026 revenues and operating EBITDA are expected to be second-half weighted due to technology transfers and the Durham facility ramp-up, creating timing risk for near-term performance - this affects investors focused on short-term biotech manufacturing revenues.
  • Despite positive operating EBITDA for 2025, the company reported a full-year operating loss of £22.50 million, reflecting ongoing profitability and cost-structure risks for stakeholders in the biotech services sector.
  • Integration and operational scaling of the Durham facility may carry execution risk that could influence the company’s projected 2026 margins and the medium-term growth trajectory in 2027-28.

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