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

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorGuangdong Hengrui Pharmaceutical Co., Ltd

About this trial

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

Eligibility criteria

Qualifiers

Age 18-75 years, regardless of gender;

Weight ≥40.0 kg at screening;

Diagnosed as primary membranous nephropathy through kidney biopsy.

Disqualifiers

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

Trial design

Treatments tested in this trial

  • SHR-2173 injection
  • SHR-2173 injection
  • SHR-2173 injection

Treatment groups

75 Participants
are divided into 3 treatment groups