This open-label, non-randomized, retrospective-prospective, non-interventional study will evaluate the efficacy and safety of Mircera in patients with stage III-IV chronic kidney disease (CKD) not on dialysis. Patients will receive open-label treatment with Mircera for 12 months at a dose to be determined by the investigator.
Study Type
OBSERVATIONAL
Enrollment
153
No intervention was administered in this study.
Unnamed facility
Belgrade, Serbia
Unnamed facility
Ćuprija, Serbia
Unnamed facility
Kragujevac, Serbia
Unnamed facility
Niš, Serbia
Percent Of Participants Who Reached And Maintained Target Hemoglobin Values During Treatment
Time frame: 12 months
Hb Levels At Start And End Of Treatment
Time frame: 12 months
Mircera Dose At Start And End Of Treatment
Time frame: 12 months
Time To Achieve Response To Mircera
Time frame: 12 months
Percent Of Participants Treated With Iron Supplements
Time frame: 12 months
Percent of Participants Who Required Transfusion At Start And End Of Treatment
Time frame: 12 months
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Unnamed facility
Pirot, Serbia
Unnamed facility
Požarevac, Serbia
Unnamed facility
Sremska Mitrovica, Serbia
Unnamed facility
Šabac, Serbia
Unnamed facility
Užice, Serbia
Unnamed facility
Zrenjanin, Serbia