Status:

TERMINATED

A Study of NeoRecormon (Epoetin Beta) in Patients With Renal Anemia.

Lead Sponsor:

Hoffmann-La Roche

Conditions:

Anemia

Eligibility:

All Genders

18-80 years

Phase:

PHASE4

Brief Summary

This study will determine whether 8 weekly monitoring of hemoglobin and iron parameters in the correction phase of NeoRecormon therapy in patients with renal anemia is as safe and effective as 4 weekl...

Eligibility Criteria

Inclusion

  • adult patients, 18-80 years of age;
  • stage 3-4 chronic kidney disease (eGFR 15-60mL/min);
  • Hb \<100g/L, TSAT\>=20%, and ferritin \>=100 mcg/L at screening.

Exclusion

  • anticipating to go on renal replacement therapy;
  • anticipating a living related-donor kidney transplant, or a prior recipient of a kidney transplant;
  • uncontrolled hypertension;
  • congestive heart failure;
  • active bleeding or red blood cell transfusions in 8 weeks prior to screening; systematic hematological disease.

Key Trial Info

Start Date :

Trial Type :

INTERVENTIONAL

End Date :

Estimated Enrollment :

Patients enrolled

Trial Details

Trial ID

NCT00440063

Last Update

December 20 2007

Active Locations (9)

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Page 1 of 3 (9 locations)

1

Adelaide, Australia

2

Gosford, Australia

3

Herston, Australia

4

Liverpool, Australia

A Study of NeoRecormon (Epoetin Beta) in Patients With Renal Anemia. | DecenTrialz