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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