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Clinical Trials in China / NCT07289763
Recruiting Phase 2

Phase II Randomized, Open-label, Multicenter Clinical Study Evaluating the Safety, Efficacy, Pharmacokinetics, and Pharmacodynamics of SHR-2173 Injection in Patients With Primary Membranous Nephropathy

NCT07289763 · tracked via the Priya Life Science China tracker
Sponsor
Guangdong Hengrui Pharmaceutical Co., Ltd
Phase
Phase 2
Started
2025-12-31
Last updated
2026-01-26

Condition(s) studied

Primary Membranous Nephropathy

Investigational drug(s) / intervention(s)

SHR-2173 injectionSHR-2173 injectionSHR-2173 injection

SHR-2173 injection: SHR-2173 injection, with a total of 8 administrations

SHR-2173 injection: SHR-2173 injection, with a total of 16 administrations

SHR-2173 injection: SHR-2173 injection , with a total of 32 administrations

Study summary

To investigate the safety, efficacy, pharmacokinetics, and pharmacodynamics of SHR-2173 injection in patients with primary membranous nephropathy

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age 18-75 years, regardless of gender; 2. Weight ≥40.0 kg at screening; 3. Diagnosed as primary membranous nephropathy through kidney biopsy. Exclusion Criteria: 1. Secondary membranous nephropathy. 2. Subjects developed rapidly progressive glomerulonephritis or required kidney transplantation. 3. Subjects who have undergone kidney dialysis in the previous 12 months or are expected to require dialysis during the study period. 4. Subjects who have a malignant tumor or a history of malignant tumor 5. Subjects who have undergone major surgery within the previous 3 months, or plan to undergo major surgery during the study period.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
General hospital of eastern theater command Nanjing Jiangsu Recruiting

More Guangdong Hengrui Pharmaceutical Co., Ltd trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07289763 on ClinicalTrials.gov ↗ ← All trials in China