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NOT YET RECRUITING
NCT06635772
PHASE2

A Study of the Effect and Safety of HS-10390 in the Treatment of Patients with Primary IgA Nephropathy

Sponsor: Hansoh BioMedical R&D Company

View on ClinicalTrials.gov

Summary

This study will evaluate the efficacy and safety of HS-10390 in subjects with primary IgA nephropathy, and explore the optimal dose for the treatment.

Official title: A Randomized, Multicenter, Open-label, Active-control Study of the Efficacy and Safety of HS-10390 for the Treatment of Immunoglobulin a Nephropathy

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

90

Start Date

2024-11

Completion Date

2026-04-30

Last Updated

2024-10-10

Healthy Volunteers

No

Interventions

DRUG

HS-10390

HS-10390 will be administered daily

DRUG

Irbesartan

Irbesartan will be administered daily as a 150-mg oral tablet. For patients who tolerate the initial dose of 150 mg after 2 weeks will increase their dose to 300 mg

Locations (1)

Peking University First Hospital

Beijing, China