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

PHASE2CompletedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

October 6, 2017

Primary Completion Date

May 3, 2019

Study Completion Date

February 3, 2020

Conditions
Lupus Membranous Nephropathy
Interventions
DRUG

Filgotinib

200 mg tablet administered orally once daily

DRUG

Lanraplenib

30 mg tablet administered orally once daily

DRUG

Filgotinib placebo

Tablet administered orally once daily

DRUG

Lanraplenib placebo

Tablet administered orally once daily

Trial Locations (7)

30046

Georgia Nephrology Research Institute, Lawrenceville

30303

Emory University School of Medicine, Atlanta

35294

University of Alabama at Birmingham (UAB), Birmingham

48109

University of Michigan, Ann Arbor

94304

Stanford University, Palo Alto

32610-0272

University of Florida, Gainesville

27599-7155

University of North Carolina at Chapel Hill / UNC School of Medicine, Chapel Hill

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Gilead Sciences

INDUSTRY

NCT03285711 - Study to Evaluate the Safety and Efficacy of Filgotinib and Lanraplenib in Adults With Lupus Membranous Nephropathy (LMN) | Biotech Hunter | Biotech Hunter