Clinical Trial

A Phase I Study of YK012 in Primary Membranous Nephropathy

Not Yet Recruiting Phase 1
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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 2025-11-14.
Trial Details
NCT Number NCT07234474
Lead Sponsor Excyte Biopharma Ltd
Conditions Primary Membranous Nephropathy
Enrollment 66 participants
Start Date 2026-10
Primary Completion 2027-11 (estimated)
Study Completion 2028-02 (estimated)
Updated on ClinicalTrials.gov 2026-02-05