A Phase I Study of YK012 in Primary Membranous Nephropathy
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).
Age 18-80 (inclusive), both gender. [+6]
Diagnosed with secondary membranous nephropathy. [+17]