drugset / Trial / NCT06720025

Study of SAL-0951 Compared to Recombinant Human Erythropoietin in Anemic Patients Receiving Maintenance Hemodialysis

NCT06720025

Phase 3 Completed 100 enrolled Shenzhen Salubris Pharmaceuticals Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and efficacy of SAL-0951 in Chinese patients undergoing maintenance hemodialysis with chronic kidney disease and anemia,who are receiving stable treatment with erythropoietic stimulants (ESAs).

Timeline

Start
2023-09-19
Primary completion
2024-06-17
Completion
2024-06-20

Drugs

EvaluationDrugModalityDoseRoute
Subject SAL-0951 Unknown 1 mg
Subject SAL-0951 Unknown 8 mg
Comparator epoetin alfa Protein / enzyme biologic

Indications