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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT03134222

Public ClinicalTrials.gov record NCT03134222. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 10:05 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Double-blind, Placebo-controlled Study to Assess the Safety and Efficacy of Filgotinib and GS-9876 in Female Subjects With Moderately-to-Severely Active Cutaneous Lupus Erythematosus (CLE)

Study identification

NCT ID
NCT03134222
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gilead Sciences
Industry
Enrollment
47 participants

Conditions and interventions

Interventions

  • Lanraplenib Drug
  • Filgotinib Drug
  • Lanraplenib placebo Drug
  • Filgotinib placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 23, 2017
Primary completion
Mar 12, 2019
Completion
Dec 17, 2019
Last update posted
Jun 8, 2020

2017 – 2019

United States locations

U.S. sites
13
U.S. states
5
U.S. cities
13
Facility City State ZIP Site status
Wallace Rheumatic Studies Center Beverly Hills California 90211
St. Jude Hospital Yorba Linda DBA Dr. Joseph Heritage Healthcare Fullerton California 92835
Dermatology Research Associates Los Angeles California 90045
Desert Medical Advances Palm Desert California 92260
Medderm Associates San Diego California 92103
Inland Rheumatology Clinical Trials Upland California 91786
Clinical Research of West Florida, Inc. Clearwater Florida 33765
Omega Research Consultants LLC DeBary Florida 32713
DJL Clinical Research, PLLC Charlotte North Carolina 28210
Wake Forest University Health Sciences Winston-Salem North Carolina 27104
Penn State Hershey Medical Center Hershey Pennsylvania 17033
University of Pennsylvania Philadelphia Pennsylvania 19104
Metroplex Clinical Research Center Dallas Texas 75231

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03134222, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 8, 2020 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03134222 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →