drugset / Trial / NCT03285711

Study to Evaluate the Safety and Efficacy of Filgotinib and Lanraplenib in Adults With Lupus Membranous Nephropathy (LMN)

NCT03285711

Phase 2 Completed 9 enrolled Gilead Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the efficacy of filgotinib and lanraplenib (previously GS-9876) in adults with lupus membranous nephropathy (LMN).

Timeline

Start
2017-10-06
Primary completion
2019-05-03
Completion
2020-02-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Filgotinib Small molecule 200 mg Oral
Subject Lanraplenib Small molecule 30 mg Oral

Indications