Clinical Trial

A First in Human Study to Evaluate Safety, Tolerability, Pharmacology of HS-10390 in Healthy Subjects

Recruiting Phase 1
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Summary
The purpose of this first in human study is to evaluate the safety, tolerability, pharmacokinetics (PK),and pharmacodynamics (PD) of HS-10390 in healthy subjects.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2023-07-04; most recent amendment 2024-10-07.
Trial Details
NCT Number NCT05942625
Lead Sponsor Hansoh BioMedical R&D Company
Conditions IgA Nephropathy, Focal Segmental Glomerulosclerosis
Enrollment 84 participants
Start Date 2023-05-23
Primary Completion 2024-06-30 (estimated)
Study Completion 2024-12-30 (estimated)
Updated on ClinicalTrials.gov 2024-10-09