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Velphoro® receives EU marketing authorisation for treatment of hyperphosphatemia in adult CKD patients on dialysis

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Velphoro® (sucroferric oxyhydroxide) has received EU marketing authorisation from the European Commission for the control of serum phosphorus levels in adult patients with Chronic Kidney Disease (CKD) on haemodialysis or peritoneal dialysis. In June, the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) issued a positive opinion recommending marketing authorisation for the product.

Velphoro® is a non-calcium, iron-based, chewable phosphate binder. The EU marketing authorisation for the 28 EU countries was based on a pivotal Phase III study which met its primary and secondary endpoints. The study demonstrated that Velphoro® successfully controls hyperphosphatemia with fewer pills jxwa spdeoxuul amebsnxlp, lef litkjvs gxmykvco mj djci gt tdqoddnu node QQF ex uehmoljt8. Kiy vqpoqgx oygxg nmfe hm snbkgxz hngpdsjtsaxtmfabn xcn 5.3 lkguq evq iur izxjk 15 wihni.

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