Study to Evaluate Safety and Efficacy of Filgotinib and Lanraplenib in Females With Moderately-to-Severely Active Cutaneous Lupus Erythematosus (CLE)
- Disease/Condition
- Cutaneous Lupus Erythematosus
- Drug/Device/Intervention
- Lanraplenib
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Gilead Sciences
- Location
- Beverly Hills,Fullerton,Los Angeles,Palm Desert,San Diego,Upland,Clearwater,DeBary,Charlotte,Winston-Salem,Hershey,Philadelphia,Dallas,Ottawa,Toronto,Waterloo, Canada,United States of America
- Phase
- Phase 2
- Start date
- May 24, 2017
- End date
- Dec 18, 2019
- Enrollment
- 47 participants
Change in Cutaneous Lupus Erythematosus Disease Area and Severity Index (CLASI) Activity Score From Baseline to Week 12
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).
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT03134222
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT03134222 through Pure Global AI's free database. This Phase 2 trial is sponsored by Gilead Sciences and is currently Completed. The study focuses on Cutaneous Lupus Erythematosus. Target enrollment is 47 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.