drugset / Trial / NCT02019719

Study to Evaluate the Safety, Efficacy and Pharmacokinetics of GSK1278863 in Japanese Hemodialysis-Dependent Subjects With Anemia Associated With Chronic Kidney Disease

NCT02019719

Phase 2 Completed 97 enrolled GlaxoSmithKline
RandomizedParallel-groupDouble-blindTreatment

Summary

This study aims to characterize the relationship between dose of GSK1278863 and hemoglobin (Hgb) response in hemodialysis-dependent (HDD) subjects with anemia associated with chronic kidney disease (CKD). It is anticipated that the data generated will enable selection of the starting dose(s) and optimize dose adjustment regimen(s) for Phase 3 clinical trials. This study will consist of a screening phase of 3-9 weeks, a 4-week treatment phase and a follow-up visit approximately 4 weeks after completing treatment.

Timeline

Start
2013-11-05
Primary completion
2014-08-06
Completion
2014-08-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Daprodustat Small molecule 4 mg Oral
Subject Daprodustat Small molecule 6 mg Oral
Subject Daprodustat Small molecule 8 mg Oral
Subject Daprodustat Small molecule 10 mg Oral

Indications