drugset / Trial / NCT03134222

Study to Evaluate Safety and Efficacy of Filgotinib and Lanraplenib in Females With Moderately-to-Severely Active Cutaneous Lupus Erythematosus (CLE)

NCT03134222

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to evaluate the efficacy of filgotinib and lanraplenib (formerly GS-9876) in females with moderately-to-severely active cutaneous lupus erythematosus (CLE).

Timeline

Start
2017-05-24
Primary completion
2019-03-13
Completion
2019-12-18

Drugs

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