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

PHASE3UnknownINTERVENTIONAL
Enrollment

175

Participants

Timeline

Start Date

June 20, 2019

Primary Completion Date

October 14, 2021

Study Completion Date

December 31, 2022

Conditions
Non-Dialysis-Dependent Chronic Kidney Disease
Interventions
DRUG

Pegol-Sihematide

Participants received Pegol-Sihematide by subcutaneous injection once every 4 weeks. The starting dose was 0.04 milligram per kilogram (mg/kg) and was adjusted throughout the study to maintain a hemoglobin target range of 10.0-12.0 grams per deciliter (g/dL).

DRUG

ESPO

Participants received ESPO by subcutaneous injection weekly. The starting dose was 6000 IU and was adjusted according to the instruction to maintain a hemoglobin target range of 10.0-12.0 grams per deciliter (g/dL).

Trial Locations (1)

510080

The First Affiliated Hospital of Sun Yat-sen University, Guangzhou

All Listed Sponsors
lead

Jiangsu Hansoh Pharmaceutical Co., Ltd.

INDUSTRY

NCT03903809 - Study of the Efficacy and Safety of Pegol-Sihematide for Anemia in Patients With NDD-CKD | Biotech Hunter | Biotech Hunter