Oxford Biomedica Expands BMS Partnership to Boost CAR-T Therapy Production

February 4, 2026
Oxford Biomedica Expands BMS Partnership to Boost CAR-T Therapy Production
  • OXB expanded its multi-year commercial supply agreement with Bristol Myers Squibb to manufacture lentiviral vectors for BMS’s CAR-T programs, marking a shift from clinical to commercial production.

  • Chris Holt of BMS highlighted OXB’s scalable, reliable manufacturing capacity as essential to meeting the growing commercial demand for CAR-T therapies.

  • OXB and BMS executives framed the contract as a milestone that provides dependable, scalable manufacturing capacity to support increasing commercial demand for CAR-T treatments.

  • Financial terms were not disclosed, but OXB expects the deal to generate meaningful multi-year revenue and support its medium-term financial guidance.

  • The collaboration agreement (CSA) is designed to deliver meaningful multi-year revenue and aligns with OXB’s medium-term guidance and strategy as a cell and gene therapy CDMO.

  • The initial term is five years with an option to extend, and commercial manufacturing is expected to begin in 2026.

  • The agreement is multi-year with a five-year initial term and includes an option to extend.

  • The collaboration began during the COVID-19 pandemic in 2020, underscoring OXB’s position as a leading cell and gene therapy CDMO with strong revenue visibility.

  • The deal expands Oxford Biomedica’s existing partnership with BMS, originally established in March 2020, and is expected to generate meaningful multi-year revenue.

  • OXB’s expansion strategy includes growing its production network, including the Durham facility acquisition and ongoing development of its Bedford AAV center of excellence.

  • The press release emphasizes OXB’s role as a global CDMO with extensive viral vector expertise and notes facilities across multiple countries.

  • The agreement supports Oxford Biomedica’s focus as a cell and gene therapy CDMO and improves long-term revenue visibility.

Summary based on 3 sources


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