Clinical Trial

Study of YK012 in Primary Membranous Nephropathy

Recruiting Phase 1
View on ClinicalTrials.gov →
Summary
The goal of this clinical trial is to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), immunogenicity, and preliminary efficacy of YK012 in participants with primary membranous nephropathy (PMN).
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-05-13.
Trial Details
NCT Number NCT06982729
Lead Sponsor Excyte Biopharma Ltd
Conditions Primary Membranous Nephropathy
Enrollment 72 participants
Start Date 2025-03-08
Primary Completion 2026-12 (estimated)
Study Completion 2027-12 (estimated)
Updated on ClinicalTrials.gov 2025-11-17