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C.E.R.A. Safety Profile: a Pooled Analysis in Patients with Chronic Kidney Disease

Overview
Journal Clin Nephrol
Specialty Nephrology
Date 2010 Feb 5
PMID 20129016
Citations 8
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Abstract

Background: C.E.R.A., a continuous erythropoietin receptor activator, is a long-acting erythropoiesis-stimulating agent (ESA) that is approved for the treatment of renal anemia. This analysis evaluated the safety profile of C.E.R.A. in comparison to that of other ESAs in patients with chronic kidney disease (CKD).

Methods: Safety parameters were analyzed in a pooled population comprising all patients with CKD on dialysis and not on dialysis from the completed Phase II and Phase III studies in the C.E.R.A. clinical program (Phase II/III population); patients were treated with either C.E.R.A. (n = 1,789) or comparator ESA (n = 948). Differences between treatment groups in safety parameters were identified by either a 2% difference in incidence between groups, or a statistically significant difference between groups (p < or = 0.05 with the Fisher's exact test, which was used as a conservative screening tool). To assess changes in safety findings over time, long-term safety data were analyzed from patients who were given the option to enter long-term safety studies upon completing their initial Phase II/III study (safety extension population).

Results: Compared with the C.E.R.A. group, the incidence of adverse events (AEs) was higher in the comparator ESA group in the Phase II/III population (C.E.R.A. vs. comparator ESA, 89.5% vs. 91.8%, p = 0.067), and significantly so in the safety extension population (93.0% vs. 95.8%, p = 0.003). The incidence of serious AEs was significantly higher in the comparator ESA group than in the C.E.R.A. group in both analysis populations (Phase II/III population, 37.8% vs. 42.4%, p = 0.021; safety extension population, 53.3% vs. 59.7%, p = 0.001). However, there was no consistent pattern of clinical events that could explain these differences between the treatment groups.

Conclusion: Analysis of safety events in patients with renal anemia receiving long-term treatment with C.E.R.A. shows a safety profile comparable to that of other ESAs.

Citing Articles

Subcutaneous C.E.R.A. for the Treatment of Chronic Renal Anemia in Predialysis Patients.

Ustundag S, Dogan E, Duranay M, Kazancioglu R, Celik V, Unsal A Balkan Med J. 2016; 33(3):322-30.

PMID: 27308077 PMC: 4898992. DOI: 10.5152/balkanmedj.2016.141173.


Once-Monthly Continuous Erythropoietin Receptor Activator (C.E.R.A.) in Patients with Hemodialysis-Dependent Chronic Kidney Disease: Pooled Data from Phase III Trials.

Locatelli F, Choukroun G, Truman M, Wiggenhauser A, Fliser D Adv Ther. 2016; 33(4):610-25.

PMID: 26965694 PMC: 4846713. DOI: 10.1007/s12325-016-0309-6.


Once-monthly continuous erythropoietin receptor activator (CERA) for haemoglobin maintenance in haemodialysis patients with chronic renal anaemia.

Duman N, Uyanik A, Unsal A, Sezer S, Camsari T, Cirit M Clin Kidney J. 2014; 7(5):464-9.

PMID: 25504109 PMC: 4257910. DOI: 10.1093/ckj/sfu079.


Beneficial dose conversion after switching from higher doses of shorter-acting erythropoiesis-stimulating agents to C.E.R.A in CKD patients in clinical practice: MINERVA Study.

Cases A, Portoles J, Calls J, Martinez-Castelao A, Munar M, Segarra A Int Urol Nephrol. 2014; 46(10):1983-95.

PMID: 25118611 DOI: 10.1007/s11255-014-0800-4.


Cost-effectiveness of continuous erythropoietin receptor activator in anemia.

Schmid H Clinicoecon Outcomes Res. 2014; 6:319-30.

PMID: 25050070 PMC: 4090042. DOI: 10.2147/CEOR.S46930.