drugset / Trial / NCT03903809

Study of the Efficacy and Safety of Pegol-Sihematide for Anemia in Patients With NDD-CKD

NCT03903809

Phase 3 Unknown 175 enrolled Jiangsu Hansoh Pharmaceutical Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the safety and efficacy of Pegol-Sihematide, as compared with recombinant human erythropoietin injection (CHO Cell), ESPO, in anemia treatment in patients with non-dialysis-dependent chronic kidney disease.

Timeline

Start
2019-06-20
Primary completion
2021-10-14
Completion
2022-12-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator ESPO Protein / enzyme biologic 6000 iu Subcutaneous
Subject Pegol-Sihematide Unknown 0.025 mg/kg Subcutaneous
Subject Pegol-Sihematide Unknown 0.04 mg/kg Subcutaneous