Abzena expands analytical capabilities to include GMP cell-based potency testing across US & UK sites

Abzena, a leading end-to-end integrated CDMO + CRO for complex biologics and bioconjugates, has announced the expansion of their early and late phase analytical capabilities to now include GMP cell-based potency assays at their Cambridge, UK and San Diego, CA development and manufacturing facilities.

GMP cell-based potency assays play an essential role in quantitatively measuring the biological activity of a biopharmaceutical, and the cytotoxicity of the payload of an antibody-drug conjugate (ADC), for both GMP product release and stability testing. By adding this capability to their global toolkit, Abzena will be able to provide precise and reliable data on drug potency, alongside developability and characterization data including mechanism of action (MOA) and immunogenicity, which are essential for regulatory submissions.

Dr Campbell Bunce, CSO and Cambridge Site Head at Abzena said, “Our established expertise and reputation have allowed us to extend our early-phase capabilities to include GMP cell-based potency services at our global sites, addressing a critical need for our customers. This significant milestone further demonstrates our commitment to providing comprehensive, end-to-end support for our customer’s next-generation programs that drive successful outcomes from discovery to the clinic and onwards towards commercial.”

Sean O’Brien, SVP & San Diego Site Head at Abzena shared,“Our goal is to help our customers optimize their drug development strategies, secure funding, and navigate regulatory pathways more effectively. We will continue to invest in our expertise and expand our laboratories so that our broader analytical offering can best support them in their mission to get life-changing medicines to patients.”

All the Cambridge, UK site’s services are fully integrated with Abzena’s development and manufacturing services at their US facilities in San Diego, CA, and Bristol, PA.

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