A PHASE 2B, RANDOMIZED, BLINDED, DOSE-RANGING, ACTIVE-CONTROLLED, PARALLEL-GROUP, MULTI-CENTER STUDY TO EVALUATE THE DOSE RESPONSE RELATIONSHIP OF GSK1278863 OVER THE FIRST 4 WEEKS OF TREATMENT AND EVALUATE THE SAFETY AND EFFICACY OF GSK1278863 OVER 24 WEEKS IN HEMODIALYSIS-DEPENDENT SUBJECTS WITH ANEMIA ASSOCIATED WITH CHRONIC KIDNEY DISEASE WHO SWITCH FROM RECOMBINANT HUMAN ERYTHROPOIETIN
- Registry ID
- PHI113633
- Source registry
- HEALTH_CANADA
- Status
- Ongoing
- Phase
- PHASE2
- Study type
- INTERVENTIONAL
- Sponsor
- GLAXOSMITHKLINE INC
- Start date
- 2014-01-07
- Last update
- 2013-09-17
Conditions
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