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Not Yet RecruitingNCT07234474

A Phase I Study of YK012 in Primary Membranous Nephropathy

A Phase I Study of YK012, a Humanized CD19 × CD3 Bispecific Antibody, in Participants With Very High-Risk, Refractory Primary Membranous Nephropathy

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
66 (estimated)
Sponsor
Excyte Biopharma Ltd · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

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).

Conditions

Interventions

TypeNameDescription
DRUGYK012YK012 is a bispecific antibody targeting CD19 on B cells and CD3 on T cells leading to T cell-mediated cytotoxicity of malignant B cells

Timeline

Start date
2026-10-01
Primary completion
2027-11-01
Completion
2028-02-01
First posted
2025-11-18
Last updated
2026-02-05

Regulatory

Source: ClinicalTrials.gov record NCT07234474. Inclusion in this directory is not an endorsement.

A Phase I Study of YK012 in Primary Membranous Nephropathy (NCT07234474) · Clinical Trials Directory