RecruitingPhase 2NCT07289763

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


Sponsor

Guangdong Hengrui Pharmaceutical Co., Ltd

Enrollment

75 participants

Start Date

Dec 31, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Inclusion Criteria3

  • Age 18-75 years, regardless of gender;
  • Weight ≥40.0 kg at screening;
  • Diagnosed as primary membranous nephropathy through kidney biopsy.

Exclusion Criteria5

  • Secondary membranous nephropathy.
  • Subjects developed rapidly progressive glomerulonephritis or required kidney transplantation.
  • Subjects who have undergone kidney dialysis in the previous 12 months or are expected to require dialysis during the study period.
  • Subjects who have a malignant tumor or a history of malignant tumor
  • Subjects who have undergone major surgery within the previous 3 months, or plan to undergo major surgery during the study period.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGSHR-2173 injection

SHR-2173 injection, with a total of 8 administrations

DRUGSHR-2173 injection

SHR-2173 injection, with a total of 16 administrations

DRUGSHR-2173 injection

SHR-2173 injection , with a total of 32 administrations


Locations(1)

General hospital of eastern theater command

Nanjing, Jiangsu, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07289763


Related Trials