This information is for providers outside of the U.S. ONLY
AAV5 Total Antibody Assay for Valoctocogene Roxaparvovec Eligibility in Hemophilia A
The AAV5 DetectCDx™ for valoctocogene roxaparvovec eligibility in Hemophilia A is a qualitative in vitro diagnostic test by electrochemiluminescence intended for detection of antibodies in human plasma collected in 3.2% sodium citrate that bind to the adeno-associated virus serotype 5 (AAV5). The AAV5 DetectCDx is indicated as an aid in the selection of adult hemophilia A patients for whom valoctocogene roxaparvovec treatment is being considered. Patients that are anti-AAV5 antibody positive (result of detected) are not eligible for treatment with valoctocogene roxaparvovec; patients that are anti-AAV5 antibody negative (result of not detected) are eligible for treatment with valoctocogene roxaparvovec. This assay is for professional use only.
Instructions for Use
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How to Order
If you are interested in ordering, please visit www.aav5detectcdx.com for more information.