Labcorp gets USFDA nod for Companion Diagnostic for use with Pfizer hemophilia B Gene Therapy

An estimated 6,000 people in the United States are living with hemophilia B, which is a rare inherited bleeding disorder that prevents normal blood clotting due to a deficiency in Factor IX (FIX), which causes those with the disease to bleed more frequently and longer than others. It is estimated that as many as 60% of the American population have preexisting anti-AAV antibodies, which could interfere with rAAV gene delivery, demonstrating the essential need for nAbCyte CDx testing prior to treatment with BEQVEZ.

"The approval of the nAbCyte companion diagnostic represents a first for a gene therapy that treats eligible patients with hemophilia B, helping to bring clarity to physicians and patients who are considering BEQVEZ as a treatment option," said Dr. Sonal Bhatia, M.D., Head of U.S. Specialty Care Medical Affairs, Pfizer. "We believe this companion diagnostic is an important tool for evaluating patients who may be suitable for gene therapy as the treatment paradigm advances with the introduction of gene therapies like BEQVEZ."

The results from the nAbCyte test will be reported qualitatively as negative (not detected) or positive (detected). A negative test result indicates that an individual with moderate to severe hemophilia B can be considered for BEQVEZ therapy.

The FDA approval of nAbCyte Anti-AAVRh74var HB-FE CDx builds on Labcorp's comprehensive cell and gene therapy solutions, including specialized pre-clinical toxicology, biomarker and CDx development, and post-commercialization capabilities.

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