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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


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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