drugset / Trial / NCT03903809
Study of the Efficacy and Safety of Pegol-Sihematide for Anemia in Patients With NDD-CKD
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |