CSL Behring Presents Phase III Data for IDELVION for Hemophilia B

Note: The below is an edited version of an article originally published on Yahoo Finance. The original release can be read in it’s entirety here.
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CSL Behring announced new data today from its Phase III PROLONG-9FP clinical development program evaluating IDELVION^® [Coagulation Factor IX (Recombinant), Albumin Fusion Protein], the company’s long-acting recombinant albumin fusion protein for treating hemophilia B. The data, from a Phase III study and an ongoing extension study, assessed the long-term efficacy and safety of IDELVION for routine prophylaxis in previously treated children and adults with hemophilia B. The results showed that extended prophylaxis treatment regimens effectively prevented bleeds while also reducing overall IDELVION consumption.