# Croda International U.S. government to support lipid systems expansion

- Link: https://www.directorstalkinterviews.com/croda-international-u.s.government-to-support-lipid-systems-expansion/4121070329
- Published: 2022-06-28T07:24:57+01:00
- Author: Amilia Stone

**[Croda International Plc](https://www.directorstalkinterviews.com/ftse-company/croda-international/crdo.l)**(
LON:CRDA), the company that uses smart science to create high performance ingredients
and technologies that improve lives, has announced that it has entered into a cooperative
agreement with the United States government in which the government will provide
up to $75 million to expand the company’s U.S. manufacturing capacity of ingredients
for lipid systems used in novel therapeutic drugs, such as mRNA vaccines.

In line with the company’s strategy to ‘Empower Biologics Delivery,’ Croda will 
also invest up to $58 million, bringing the total project investment to up to $133
million. This spend is included within the company’s existing capital expenditure
programme, outlined in the 2021 annual results.

The investment will be used to establish a new lipid facility as part of a new multi-
purpose cGMP_^(*)_ site in Lamar, Pennsylvania. Construction is expected to start
later this year, with the new capacity anticipated in 2025. The investment supports
expansion of the portfolio of patient health care solutions offered by Croda, by
creating a third manufacturing site for lipid systems, alongside Croda’s existing
Alabaster, Alabama, U.S. (Avanti) and Leek, United Kingdom capabilities.

The cooperative agreement is a joint award from the Biomedical Advanced Research
and Development Authority (BARDA), part of Office of the Assistant Secretary for
Preparedness and Response within the U.S. Department of Health and Human Services
and the U.S. Department of Defense’s Joint Program Executive Office for Chemical,
Biological, Radiological and Nuclear Defense (JPEO-CBRND) in partnership with the
Army Contracting Command’s Joint COVID Response Division (ACC JCRD). The new facility
is part of a programme to expand the U.S. industrial base supporting critical vaccine
and therapeutic manufacturing activities. The facility at Lamar will support U.S.
preparedness for future health emergencies, by ensuring enough capacity is available
in the U.S. to produce the necessary components for vaccine manufacture.    

Croda’s Pharma business is a leading partner in the development of delivery systems
for biologics. Croda’s platforms enable the next generation of vaccines and therapeutics.
Through acquisition of Avanti Polar Lipids in 2020, Croda was the first company 
to supply clinical and commercial quantities of critical lipid systems to support
the roll-out of COVID-19 vaccines globally.

Lipid systems offer significant potential as the delivery system for a wide range
of nucleic acid applications, including novel mRNA-based therapeutics, such as flu
vaccines and cancer treatments. Given the scale of the current clinical development
pipeline, the market for lipid systems is expected to grow significantly over the
next ten years.

> **Commenting, Daniele Piergentili, President of Croda Life Sciences, said**: _“
> We are grateful to the U.S. government for its support of Croda. The delivery 
> technology based on lipid systems offers significant potential for the safe and
> efficient delivery of next generation vaccines and therapeutic drugs. As a result
> of this investment, Croda will be able to expand its capabilities to develop and
> manufacture ingredients in support of this important technology. This will help
> ensure that the U.S. is well prepared for future health emergencies and equipped
> to offer advanced treatments for some of the most prevalent illnesses in the world
> today.”_

> **Nicole Kilgore, Deputy Joint Program Executive Officer (JPEO) for Chemical, 
> Biological, Radiological and Nuclear (CBRN) Defense, said**: _“The U.S. government
> is pleased to be a part of these Industrial Base Expansion efforts to expand production
> of raw materials for mRNA vaccines.”_

_^(*)cGMP is ‘current Good Manufacturing Practice’, the U.S. Food and Drug Administration’s(
FDA’s) most stringent requirement for the manufacture of pharmaceutical products._

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