HEC53856 Phase Ib Study in Patients With Non-dialysis Renal Anemia

Status Not yet recruiting

Clinical Trial Summary

To evaluate the safety, tolerability , pharmacokinetics and Preliminary Efficacy of HEC53856 Capsules in Patients With Non-dialysis Renal Anemia.

Clinical Trial Description

This is a MultiCenter, Randomized, Blinded, Active Drug and Placebo-controlled, Dose-escalated Phase Ib Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of HEC53856 Capsules in Patients With Non-dialysis Renal Anemia. Each part participants will be randomly administrated for HEC53856 or placebo or roxadustat. The study consisted of three study periods as follows: Screening period: up to 2 weeks； Treatment period: 8 weeks； Post-Treatment Follow-Up period: 4 weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04925661
Study type	Interventional
Source	Sunshine Lake Pharma Co., Ltd.
Contact
Status	Not yet recruiting
Phase	Phase 1
Start date	September 29, 2021
Completion date	May 10, 2023

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