Keryx Biopharmaceuticals

Keryx initiates phase II study of Zerenex in chronic kidney disease

Thursday, November 1, 2012 10:25 AM

Keryx Biopharmaceuticals, a biopharmaceutical company based in New York, N.Y., has initiated a phase II study of Zerenex (ferric citrate), the company's ferric iron-based phosphate binder drug candidate, in managing serum phosphorus and iron deficiency in anemic patients with Stage 3 to 5 non-dialysis dependent chronic kidney disease (NDD-CKD).

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Keryx completes patient enrollment for phase III Zerenex trial

Monday, September 19, 2011 12:28 PM

Keryx Biopharmaceuticals has completed patient enrollment in the long-term study component of its phase III registration program of Zerenex, the company's ferric iron-based phosphate binder for the treatment of elevated serum phosphorus levels, or hyperphosphatemia, in patients with end-stage renal disease (ESRD) on dialysis. The Zerenex phase III registration program, which is being conducted pursuant to a Special Protocol Assessment (SPA) with the FDA, is comprised of an already successfully-completed phase III short-term study, and this ongoing phase III long-term study.

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Keryx reports positive results in renal disease study

Friday, April 29, 2011 11:25 AM

Keryx Biopharmaceuticals reports the final dataset from the phase III short-term clinical trial of Zerenex (ferric citrate) for the treatment of hyperphosphatemia in 151-end-stage renal disease patients on dialysis. 

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