drugset / Trial / NCT01977482
Evaluation of Dose Response Relationship, Safety and Efficacy of GSK1278863 in Hemodialysis-dependent Subjects With Chronic Kidney Disease Associated Anemia
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 | — | — |