The U.S. Food and Drug Administration has approved Sanofi's Qfitlia (fitusiran) for routine prophylaxis to prevent or reduce ...
The FDA has recently approved two new prophylactic treatments for people with hemophilia who develop antibodies to clotting ...
Unlike other hemophilia therapies, Qfitlia is indicated for both hemophilia A and B, and can be given in patients regardless ...
The US Food and Drug Administration has approved fitusiran for bleeding prophylaxis in hemophilia A and B with or without ...
Fitusiran is a small interference RNA therapeutic designed to prevent bleeds in patients with hemophilia A or B by lowering antithrombin.
Over the last three years, the FDA has approved six new hemophilia drugs, including three gene therapies. | Over the last ...
The U.S. Food and Drug Administration on Friday approved Sanofi SA’s (NASDAQ:SNY) Qfitlia (fitusiran), the first antithrombin ...
The FDA has approved fitusiran, now named Qfitlia, for routine prophylaxis in patients aged 12 and older with hemophilia A or ...
Hemophilia A and hemophilia B are genetic bleeding disorders caused by a dysfunction or deficiency of coagulation factor VIII (FVIII) or IX (FIX), respectively. Patients with these hemophilias are ...
Subcutaneous Qfitlia does not replace the missing coagulation factor VIII or IX ... 177 adult and pediatric male patients with either hemophilia A or hemophilia B. Among participants with ...
"Today's approval of Qfitlia is significant for patients with hemophilia because it can ... treatment with bypassing agents (BPAs) or clotting factor concentrates. In the two trials -- ATLAS ...
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