The new blood-based screening tool represents an alternative to a standard clot-based FVIII test which cannot accurately determine inhibitor levels in patients receiving Hemlibra®.
Shelby Dietrich, MD, helped establish one of the first hemophilia treatment centers in the US.
Much of the data for this analysis was drawn from the HAVEN clinical trial program, which was designed to assess the efficacy and safety of emicizumab in hemophilia A patients with and without FVIII inhibitors.
The AAVs being being investigated are designed to target the human liver, drawing on the organs potential to produce clotting factor.
Bayer has responded to NHF's and HFA's queries regarding the recall.
Meet the team who are dedicating their 26-mile run to NHF.
Bayer has responded to NHF and HFA's questions about the recall of Kogenate® FS.
The company is developing gene therapies for both hemophilia A and B, and for several other chronic conditions.
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