Indevus reports positive Phase III results for Supprelin LA
This study evaluated the two-year safety and efficacy of Supprelin LA in children who received a second implant following an initial year of therapy. The study found that
Kyowa Kirin subsidiary Kyowa Kirin EMEA has received approval from the European Commission (EC) to expand the use of Crysvita (burosumab) for treating X-linked hypophosphataemia (XLH) in infants aged one month to one year across the EU and European Economic Area.