Curia acquires Integrity Bio for fill-finish expansion


The company’s biologic capabilities are complementary with Curia’s existing business, the CDMO says

Curia, formerly AMRI, an international CDMO, has entered into a definitive agreement to acquire Integrity Bio, a privately held formulation and fill-finish company headquartered in Camarillo, California.

The company specialises in hard-to-formulate biologics and fill-finish of therapies in preclinical and clinical development. In a typical year, the company says, it formulates more than 60 large molecules including proteins, antibodies, lipid nanoparticles, peptides and vaccines in liquid and lyophilised form. It also recently expanded its facilities to include a second fill-finish line, which more than doubled its manufacturing capacity.

The company’s biologic capabilities are complementary with Curia’s existing business, the CDMO says, which currently provides customers with integrated solutions from formulation development through fill-finish commercial manufacturing across three facilities in Albuquerque, New Mexico; Burlington, Massachusetts and Glasgow, Scotland.

“Curia has decades of experience in managing complexity from R&D through manufacturing,” said Curia Chairman and CEO John Ratliff. “I’m looking forward to welcoming the Integrity Bio team. The addition of Integrity Bio is a great fit with our growth strategy and our existing expertise, enhancing our biologics drug product formulation development as well as our fill-finish network. Integrity Bio also adds West Coast coverage to Curia’s East Coast and European capabilities. Together, we can make an even bigger impact on patients’ lives.”

“We are very excited about this transaction; the strategic fit is sound,” said Michael Reilly, CEO of Integrity Bio. “As part of Curia, we can now offer our customers not only world-class formulation and fill-finish but also world-class commercial manufacturing.”

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The transaction is expected to close in the third quarter.

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