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FDA clears Affymax Omontys injection

The US Food and Drug Administration (FDA) has approved Affymax's Omontys (peginesatide) injection indicated for the treatment of anemia due to chronic kidney disease (CKD) in adult patients on dialysis.

Omontys injection is a synthetic, pegylated, peptide-based erythropoiesis stimulating agent (ESA).

Nektar provides its partner Affymax with its proprietary PEGylation technology for use in Omontys.

Two Phase 3 dialysis studies (EMERALD 1 and 2) evaluated the safety and efficacy of Omontys, dosed once monthly, compared to epoetin alfa or beta, dosed one-to-three times per week.

In the studies, the primary efficacy endpoint was a mean change in Hb between baseline and evaluation period following entry into the study.