“We are very pleased that the FDA has approved the heart failure label extension of Injectafer®, and congratulate our partner on this milestone”, said Hervé Gisserot, General Manager of CSL Vifor. “Every second patient with chronic heart failure suffers from iron deficiency, with a significant number of patients either not being diagnosed or inadequately treated for iron deficiency. We are confident that Injectafer® can make a meaningful contribution to achieve key therapeutic goals in the treatment of these patients.”
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