Targeted Therapy Using Intradermal Injection of Etanercept for Remission Induction in Discoid Lupus Erythematosus
NCT02656082 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 25
Last updated 2019-02-27
Summary
The purpose of this study is to determine whether Etanercept which is given through intradermal injection is effective in the treatment of discoid lupus erythematosus (DLE).
The investigators also would like to develop new tests to measure skin inflammation by scanning the affected skin using optical coherence tomography (OCT), thermography and laser doppler imaging (LDI) and taking photographs of the rash (to be done before and after treatment). If the findings from these new tests are similar to the ones from taking a sample of skin (biopsy), then the latter (which is an invasive test) can be avoided.
Conditions
- Lupus Erythematosus, Discoid
- Lupus Erythematosus, Cutaneous
- Lupus Erythematosus, Chronic Cutaneous
Interventions
- DRUG
-
Etanercept
Treatment with etanercept is intended for remission induction of DLE only and not for maintenance purpose.
Sponsors & Collaborators
-
National Institute for Health Research, United Kingdom
collaborator OTHER_GOV - collaborator INDUSTRY
-
Clinical Trials Research Unit, Leeds
collaborator UNKNOWN -
University of Leeds
lead OTHER
Principal Investigators
-
Paul Emery, MD FMedSci · University of Leeds
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-02-01
- Primary Completion
- 2017-12-31
- Completion
- 2017-12-31
Countries
- United Kingdom
Study Locations
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