GLP-1 drug demand sees €900M investment from CordenPharma

The expansion will cover existing facilities as well as brand new constructions. CordenPharma aims for all its facilities to meet the most stringent quality and technical standards for the manufacturing of peptides with pharmaceutical purposes, including biological license application (BLA) requirements to facilitate the approval of biological products.

CordenPharma’s facilities in the Colorado, US site will expand to increase its large-scale peptide manufacturing capacity. With this expansion, the company intends to meet the increasing demand for GLP-1 peptides, a drug class used to treat type 2 diabetes and obesity.

In Europe, the CDMO is planning to build a greenfield site for small to large-scale peptide development and manufacturing, which will be fully integrated with the company’s global network of current good manufacturing practices (cGMP) facilities.

CordenPharma has an ambitious target to reach €1 billion in sales for its peptide platform by 2028, establishing itself as a market leader in both injectable and oral peptide manufacturing. In 2023, the company reported €880 million in total sales.

Corden Pharma currently has multiple long-term manufacturing contracts related to GLP-1 peptides, totaling around €3 billion.

Keeping up with GLP-1 demand

Demand for GLP-1 drugs has been high since the FDA approved Novo Nordisk’s Wegovy as a treatment for chronic weight management in 2021. Since the launch, Novo has been struggling to keep up with the supply, partly due to issues at the manufacturing facilities of Catalent, the CDMO responsible for filling the Wegovy self-injection pens.

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