drugset / Trial / NCT01977482

Evaluation of Dose Response Relationship, Safety and Efficacy of GSK1278863 in Hemodialysis-dependent Subjects With Chronic Kidney Disease Associated Anemia

NCT01977482

Phase 2 Completed 216 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindTreatment

Summary

This study is intended 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 to maintain hemoglobin (Hgb) level in hemodialysis-dependent (HDD) subjects with anemia associated with chronic kidney disease (CKD) who are switched from a stable dose of recombinant human erythropoietin (rhEPO). The data generated will enable selection of the starting dose(s) and optimize dose adjustment regimen(s) for Phase 3 clinical trials.

Timeline

Start
2013-11-01
Primary completion
2015-02-01
Completion
2015-02-06

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
Subject Daprodustat Small molecule 12 mg Oral
Comparator rhEPO Protein / enzyme biologic

Indications