drugset / Trial / NCT06830395

Study of CM313 in Subject With IgA Nephropathy

NCT06830395

Phase 2 Not yet recruiting 106 enrolled Keymed Biosciences Co.Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is divided into two parts (Part A and Part B). This study aims to evaluate the safety and efficacy of CM313 in subjects with primary Immunoglobulin A nephropathy(IgAN), while also observing its Pharmacokinetics(PK) characteristics, Pharmacokinetics(PD) effects, and immunogenicity.

Timeline

Start
2025-09
Primary completion
2027-03
Completion
2028-08

Drugs

EvaluationDrugModalityDoseRoute
Subject LUMROTATUG Monoclonal antibody Subcutaneous