The U.S. Food and Drug Administration approved French drugmaker Sanofi's hemophilia therapy, introducing a new type of ...
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 approved Qfitlia for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adult ...
FDA approves Sanofi's RNAi hemophilia drug fitusiran, licensed from Alnylam, to treat both hemophilia A and B by lowering ...
A similar regulatory filing for the drug is currently under review by the EMA, which is also supported by data from these studies. Per Sanofi, the above results make tolebrutinib the first and the ...
The U.S. Food and Drug Administration is evaluating under priority review the regulatory submission of tolebrutinib to treat non-relapsing ...
A similar regulatory filing for the drug is currently under review by the EMA, which is also supported by data from these studies. Per Sanofi, the above results make tolebrutinib the first and the ...