Phadia AB First Company to Receive FDA Clearance of Recombinant Allergen Component Tests
6/20/2011 10:20:36 AM
PORTAGE, Mich.--(BUSINESS WIRE)--Phadia, the global leader in allergy and autoimmunity diagnostics, today announced the FDA clearance of recombinant ImmunoCAP® Allergen Components for marketing in the United States. The FDA clearance applies to all of Phadia’s instrument platforms.
Phadia was the first diagnostics company to introduce allergen component testing globally and the company will continue to lead and advance the understanding of allergen component testing and its clinical application. Today’s announcement highlights the continued leadership role that Phadia plays in the evolution of innovative allergy diagnostic tools to support improved patient care. The FDA clearance covers 13 components (9 recombinants and 4 natives) including peanut, cat dander, dust mite, bermuda grass, ragweed and the mold Alternaria alternata. Phadia has a significant number of additional ImmunoCAP Allergen Component tests that will be submitted to the FDA this year.
“There is a need for greater understanding of the risk of clinical reactions. Recent studies suggest that component testing will help allergy and immunology specialists assess the risk of clinical reactions. There is much to learn and the allergy and immunology community is in a perfect position to take the lead in helping to interpret information gained from allergen component test results,” says Dr. Hugh A. Sampson, Professor of Pediatrics at the Mount Sinai School of Medicine and Director of the Jaffe Food Allergy Institute.
ImmunoCAP® Specific IgE blood tests are considered the assay of choice among specialists, and referenced and supported in over 4,000 scientific publications. Today more than 80 components are available in Europe; ImmunoCAP recombinant allergen components have been used for over 10 years and native components have been used for over 30 years.
David Esposito, President and General Manager of Phadia US, said, “Allergen component testing is the most important new technology in advancing the care of patients with allergies and asthma. By identifying the specific molecule within the allergen causing the allergic reaction, clinicians have more information than ever to enhance patient care. Allergen component test results have the potential to assess risk for reaction, explain symptoms due to cross reactivity, and identify a more targeted approach for patients requiring immunotherapy. This can improve health outcomes, and provide patient allergy and asthma action plans that make meaningful improvements in quality of life.”
Phadia has plans to accelerate its ongoing commitment to educate clinicians and patients on the use of ImmunoCAP test results to support improved patient care. Phadia continues to reinforce a guidelines-based care approach with its education efforts and most recently began a significant education effort to clinicians on the recently released NIH Guidelines for the Diagnosis and Management of Food Allergy in the US. The NIH Guidelines highlights the advantages of ImmunoCAP Specific IgE testing compared to other technologies by stating “the predictive values associated with clinical evidence of allergy for ImmunoCAP cannot be applied to other test methods.”
Phadia AB is a global leader in allergy, asthma and autoimmunity diagnostics. Phadia develops, manufactures and markets complete blood test systems to manage and support clinical diagnosis. Phadia has marketing companies in more than 20 countries and distributors in more than 60 countries. For more information please visit www.phadia.com
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