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Trials / Unknown

UnknownNCT00797784

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

A Phase 2 Open Label Study to Assess the Efficacy and Safety of Etanercept (Enbrel®)for the Treatment of Discoid Lupus Erythematosus

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Florida Academic Dermatology Centers · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

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

Conditions

Interventions

TypeNameDescription
DRUGetanercept(Enbrel®)etanercept(Enbrel®) 50mgs subcutaneous (SC) injections twice weekly for 20 weeks

Timeline

Start date
2008-10-01
Primary completion
2011-04-01
Completion
2011-04-01
First posted
2008-11-25
Last updated
2010-05-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00797784. Inclusion in this directory is not an endorsement.

The Safety and Efficacy of Etanercept (Enbrel®) for the Treatment of Discoid Lupus Erythematosus (NCT00797784) · Clinical Trials Directory