Document Detail


Once-monthly subcutaneous C.E.R.A. maintains stable hemoglobin control in patients with chronic kidney disease on dialysis and converted directly from epoetin one to three times weekly.
MedLine Citation:
PMID:  17699476     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: C.E.R.A., a continuous erythropoietin receptor activator, is in development to provide anemia correction and stable maintenance of hemoglobin (Hb) levels at extended administration intervals in patients with chronic kidney disease (CKD). This study examined its efficacy and safety when administered up to once monthly in patients who have CKD and are on dialysis and randomly convert directly from epoetin alpha or beta one to three times weekly. DESIGN, SETTING, PARTICIPANTS, AND MEASUREMENTS: In this three-arm, comparator-controlled, open-label, randomized, parallel-group, Phase III study, 572 dialysis patients (> or =18 yr) who were receiving stable subcutaneous epoetin one to three times weekly were randomly assigned (1:1:1) to continue epoetin or to receive subcutaneous C.E.R.A. once monthly or twice monthly for 52 wk. Dosage was adjusted to maintain Hb +/-1.0 g/dl of baseline level. Primary end point was mean change in Hb level between baseline and the evaluation period (weeks 29 to 36). RESULTS: Mean Hb levels during the evaluation period were similar between groups (once-monthly C.E.R.A. 11.5 g/dl; twice-monthly C.E.R.A. 11.7 g/dl; epoetin 11.5 g/dl). The difference between C.E.R.A. and epoetin in mean change (97.5% confidence interval) in Hb concentration between baseline and evaluation was -0.022 g/dl (-0.262 to 0.217) for once monthly and 0.141 g/dl (-0.098 to 0.380) for twice monthly. Analysis demonstrated that C.E.R.A. was as effective as epoetin in maintaining Hb and was well tolerated. CONCLUSIONS: Subcutaneous C.E.R.A. once or twice monthly successfully maintained tight and stable Hb levels in patients who were on dialysis and randomly converted directly from epoetin one to three times weekly.
Authors:
Wladyslaw Sulowicz; Francesco Locatelli; Jean-Philippe Ryckelynck; Jozsef Balla; Botond Csiky; Kevin Harris; Patricia Ehrhard; Ulrich Beyer;
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Publication Detail:
Type:  Clinical Trial, Phase III; Journal Article; Multicenter Study; Randomized Controlled Trial; Research Support, Non-U.S. Gov't     Date:  2007-05-23
Journal Detail:
Title:  Clinical journal of the American Society of Nephrology : CJASN     Volume:  2     ISSN:  1555-905X     ISO Abbreviation:  -     Publication Date:  2007 Jul 
Date Detail:
Created Date:  2007-08-16     Completed Date:  2007-09-25     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101271570     Medline TA:  Clin J Am Soc Nephrol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  637-46     Citation Subset:  IM    
Affiliation:
Clinic of Nephrology Collegium Medicum, Jagiellonian University, Cracow, Poland. wladsul@mp.pl
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MeSH Terms
Descriptor/Qualifier:
Anemia / blood*,  drug therapy*,  etiology
Chronic Disease
Drug Administration Schedule
Epoetin Alfa / therapeutic use*
Erythropoietin / administration & dosage*
Erythropoietin, Recombinant / therapeutic use*
Female
Hematinics / therapeutic use*
Hemoglobins / analysis*
Humans
Injections, Subcutaneous
Kidney Diseases / blood*,  complications
Male
Middle Aged
Polyethylene Glycols / administration & dosage*
Renal Dialysis*
Chemical
Reg. No./Substance:
0/Erythropoietin, Recombinant; 0/Hematinics; 0/Hemoglobins; 0/Polyethylene Glycols; 0/continuous erythropoietin receptor activator; 0/epoetin beta; 11096-26-7/Erythropoietin; 113427-24-0/Epoetin Alfa

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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