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Clinical Trial Summary

This is a multicenter, non-randomized, open-label, parallel-controlled study. The main objective is to evaluate the safety and pharmacokinetics of HRS-1780 in subjects with mild and moderate renal impairment versus healthy subjects, and to provide a basis for dose selection of HRS-1780 in patients with chronic kidney disease.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06039254
Study type Interventional
Source Shandong Suncadia Medicine Co., Ltd.
Contact Yue Fei
Phone 0518-82342973
Email yue.fei@hengrui.com
Status Not yet recruiting
Phase Phase 1
Start date September 2023
Completion date December 8, 2023

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