A Phase IIB, 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
Latest Information Update: 30 Jan 2023
At a glance
- Drugs Daprodustat (Primary) ; Recombinant erythropoietin
- Indications Anaemia; Kidney disorders
- Focus Therapeutic Use
- Sponsors GlaxoSmithKline; GSK
- 31 Mar 2015 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
- 22 Aug 2014 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.
- 09 Dec 2013 New source identified and integrated (European Clinical Trials Database: EudraCT2013-002682-19).