drugset / Trial / NCT05707377

A Study to Examine the Efficacy and Safety of Zanubrutinib Given to Adults With Primary Membranous Nephropathy

NCT05707377

Phase 2/3 Active not recruiting 178 enrolled BeOne Medicines
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objectives of this study are: In Part 1 to evaluate the efficacy of zanubrutinib as measured by proteinuria reduction, and in Part 2 to evaluate the efficacy of zanubrutinib compared with tacrolimus as measured by complete remission rate, in participants with primary membranous nephropathy (PMN) who are on optimal supportive care.

Timeline

Start
2023-04-17
Primary completion
2027-10
Completion
2027-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Tacrolimus Small molecule Oral
Subject Zanubrutinib Small molecule Oral