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The Safety and Efficacy of Etanercept (Enbrel®) for the Treatment of Discoid Lupus Erythematosus (DISCLUP2008)

Primary Purpose

Discoid Lupus Erythematosus (DLE)

Status
Unknown status
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
etanercept(Enbrel®)
Sponsored by
Florida Academic Dermatology Centers
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Discoid Lupus Erythematosus (DLE)

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Subjects with discoid lupus erythematosus .Subjects require to have confirmation of diagnosis by a skin biopsy .This can be undertaken at the screening visit if no previous biopsy confirmation available.

And;

  • Having failed steroids (topical, intralesional, systemic) and are candidates for antimalarial therapy
  • Negative ANA

Have no history of latent or active TB prior to screening.

Exclusion Criteria:

  • Subjects allergic to sunscreens
  • Prior treatment with anti-TNF therapies
  • Subjects who do not have a previous skin biopsy result confirming a DLE diagnosis and who are unwilling to undergo this procedure at screening.
  • Subjects currently receiving systemic steroid therapy (or have received in the last 3 months)
  • Known hypersensitivity to Enbrel® (etanercept) or any of its components or known to have antibodies to etanercept.
  • Prior or concurrent use of cyclophosphamide therapy
  • Concurrent sulfasalazine therapy.
  • Known HIV-positive status or known history of any other immuno-suppressing disease.
  • Any mycobacterial disease or high risk factors for tuberculosis (TB), such as family member with TB, positive purified protein derivative (PPD) or taking anti-tuberculosis medication
  • Active or chronic infection within 4 weeks before screening visit, or between the screening and baseline visits.
  • Severe comorbidities (diabetes mellitus requiring insulin; CHF of any severity; or myocardial infarction, cerebrovascular accident or transient ischemic attack within 6 months of screening visit; unstable angina pectoris; uncontrolled hypertension (sitting systolic BP <80 mm Hg or > 160 or diastolic BP > 100 mm Hg); oxygen-dependent severe pulmonary disease; history of cancer within 5 years [other than resected cutaneous basal or squamous cell carcinoma of the skin or in situ cervical cancer])
  • Systemic lupus erythematosus, history of multiple sclerosis, transverse myelitis, optic neuritis or seizure disorder.

Sites / Locations

  • Florida Academic Dermatology CentersRecruiting

Outcomes

Primary Outcome Measures

Proportion of patients responding to study treatment using the Cutaneous Lupus Erythematous Disease Area Severity Index(CLASI)defined as a decrease of 50% form baseline.

Secondary Outcome Measures

Change from baseline to week 20 in Dermatology Life Quality Index and Pysician's Global Assessment of disease measurements

Full Information

First Posted
November 21, 2008
Last Updated
May 25, 2010
Sponsor
Florida Academic Dermatology Centers
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1. Study Identification

Unique Protocol Identification Number
NCT00797784
Brief Title
The Safety and Efficacy of Etanercept (Enbrel®) for the Treatment of Discoid Lupus Erythematosus
Acronym
DISCLUP2008
Official Title
A Phase 2 Open Label Study to Assess the Efficacy and Safety of Etanercept (Enbrel®)for the Treatment of Discoid Lupus Erythematosus
Study Type
Interventional

2. Study Status

Record Verification Date
November 2008
Overall Recruitment Status
Unknown status
Study Start Date
October 2008 (undefined)
Primary Completion Date
April 2011 (Anticipated)
Study Completion Date
April 2011 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Florida Academic Dermatology Centers

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A 20 week study to assess the safety and efficacy of etanercept(Enbrel®)for the treatment of Discoid Lupus Erythematosus

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Discoid Lupus Erythematosus (DLE)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
etanercept(Enbrel®)
Intervention Description
etanercept(Enbrel®) 50mgs subcutaneous (SC) injections twice weekly for 20 weeks
Primary Outcome Measure Information:
Title
Proportion of patients responding to study treatment using the Cutaneous Lupus Erythematous Disease Area Severity Index(CLASI)defined as a decrease of 50% form baseline.
Time Frame
20 weeks
Secondary Outcome Measure Information:
Title
Change from baseline to week 20 in Dermatology Life Quality Index and Pysician's Global Assessment of disease measurements
Time Frame
20 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Subjects with discoid lupus erythematosus .Subjects require to have confirmation of diagnosis by a skin biopsy .This can be undertaken at the screening visit if no previous biopsy confirmation available. And; Having failed steroids (topical, intralesional, systemic) and are candidates for antimalarial therapy Negative ANA Have no history of latent or active TB prior to screening. Exclusion Criteria: Subjects allergic to sunscreens Prior treatment with anti-TNF therapies Subjects who do not have a previous skin biopsy result confirming a DLE diagnosis and who are unwilling to undergo this procedure at screening. Subjects currently receiving systemic steroid therapy (or have received in the last 3 months) Known hypersensitivity to Enbrel® (etanercept) or any of its components or known to have antibodies to etanercept. Prior or concurrent use of cyclophosphamide therapy Concurrent sulfasalazine therapy. Known HIV-positive status or known history of any other immuno-suppressing disease. Any mycobacterial disease or high risk factors for tuberculosis (TB), such as family member with TB, positive purified protein derivative (PPD) or taking anti-tuberculosis medication Active or chronic infection within 4 weeks before screening visit, or between the screening and baseline visits. Severe comorbidities (diabetes mellitus requiring insulin; CHF of any severity; or myocardial infarction, cerebrovascular accident or transient ischemic attack within 6 months of screening visit; unstable angina pectoris; uncontrolled hypertension (sitting systolic BP <80 mm Hg or > 160 or diastolic BP > 100 mm Hg); oxygen-dependent severe pulmonary disease; history of cancer within 5 years [other than resected cutaneous basal or squamous cell carcinoma of the skin or in situ cervical cancer]) Systemic lupus erythematosus, history of multiple sclerosis, transverse myelitis, optic neuritis or seizure disorder.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Annika M Grant, RN, MBA
Phone
305 324 2110
Ext
210
Email
annika@fadcenter.com
Facility Information:
Facility Name
Florida Academic Dermatology Centers
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Annika M Grant, RN,MBA
Phone
305-324-2110
Ext
210
Email
annika@fadcenter.com
First Name & Middle Initial & Last Name & Degree
Francisco A Kerdel, M.D.

12. IPD Sharing Statement

Learn more about this trial

The Safety and Efficacy of Etanercept (Enbrel®) for the Treatment of Discoid Lupus Erythematosus

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