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Release issued 18th November 2011
Salisbury, UK - 18th November 2011 - the Health Protection Agency (HPA) today welcomed the news that the U.S. Food and Drug Administration (FDA) has approved the Biologics License Application (BLA) for ERWINAZETM. The application was made by the HPA's development and commercialisation partner for ErwinazeTM - EUSA Pharma. ERWINAZETM (asparaginase Erwinia chrysanthemi) is used in the treatment of acute lymphoblastic leukaemia in patients with hypersensitivity to E. coli-derived asparaginase. ERWINAZETM is currently approved in a number of countries, including Canada, the UK and several European Union member states.
Dr Roger Hinton HPA's Head of Development & Production, commented, "The HPA is extremely pleased with the announcement of the FDA's approval of ERWINAZETM. We have worked diligently to achieve this goal alongside our partners EUSA Pharma, which is key in making this important therapy readily available as rapidly as possible. Children with acute lymphoblastic leukemia may develop allergy to current asparaginase products and ERWINAZETM provides a key therapeutic alternative for this gravely ill group in several countries around the world.
"The HPA has been producing ERWINASE® for a number of years and it is currently available in many countries around the world, including the UK. This treatment has helped save the lives of thousands of children and today's approval is very positive news for patients in the U.S.
"ERWINAZE® is just one of the biopharmaceutical products produced by HPA at its manufacturing facilities at Porton Down. The agency is responsible for the development and production of a number of products which are produced both in house and in partnership with others. We will continue to offer this service to allow our expertise to be applied to others in the field of translational development of biopharmaceuticals."
About acute lymphoblastic leukemia
Acute lymphoblastic leukemia (ALL) is the most commonly diagnosed childhood cancer. ALL predominantly affects children and adolescents, with approximately 2,900 patients under the age of 20 diagnosed in the U.S. each year and around 400 in the UK. ALL treatment is complex, involving a number of stages and many drugs, and includes asparaginase as an essential component of current protocols. Paediatric treatment is often highly successful, with remission rates of over 95% and 75 - 85% of treated children surviving for at least five years without recurrence of leukemia.
About ERWINAZETM
ERWINAZETM (US Trademark) ERWINASE® (Trademark outside of the US) is an asparaginase enzyme that depletes the level of the amino acid asparagine in the bloodstream. Asparagine is essential for cell growth, and its removal from the blood inhibits the growth of cells associated with acute lymphoblastic leukemia. Asparaginase products are derived from bacteria, and approximately 15 - 20 percent of patients develop hypersensitivity to modern products derived from Escherichia coli. ERWINAZETM, which is produced by Erwinia chrysanthemi, is immunologically distinct from these therapies and is suitable for patients with hypersensitivity to E. coli-derived treatments.
About HPA
The Health Protection Agency is an independent UK organisation that was set up by the government in 2003 to protect the public from threats to their health from infectious diseases and environmental hazards. In April 2013, subject to the usual approvals procedures for establishing new bodies, the Health Protection Agency will become part of a new organisation called Public Health England, an executive agency of the Department of Health. To find out more, visit our website: www.hpa.org.uk or follow us on Twitter @HPAuk.
If you want to find out more about the company visit Health Protection Agency profile.
(15th September 2008) Funding for Design of New State of the Art Facilities at Health Protection Agency’s Porton Down Site Announced
(17th July 2008) HPA receives Capacity Building Award
(17th July 2008) Health Protection Agency to Design Laboratories for Samples from Mars
(22nd January 2007) Development of a Pan Meningococcal Vaccine for the World
(22nd November 2005) Health Protection Agency and OPi Pharmaceuticals launch drug to help children fight leukaemia
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| Nr | Query | Error | Affected | Num. rows | Took (ms) |
|---|
| Nr | Query | Error | Affected | Num. rows | Took (ms) |
|---|---|---|---|---|---|
| 1 | DESCRIBE `reports` | 17 | 17 | 1 | |
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