Efficacy and Safety of ASF-1096 Cream 0.5% in the Treatment of Discoid Lupus Erythematosus (DLE) Lesions (2)
NCT ID: NCT00625157
Last Updated: 2008-02-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
INTERVENTIONAL
Brief Summary
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The aim of this pivotal trial is to investigate the efficacy and safety of ASF-1096 cream 0.5% in the treatment of patients with DLE or SLE presenting newly developed discoid lesions.
Detailed Description
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Conditions
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Study Design
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TREATMENT
Study Groups
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1
ASF 1096 0.5 % cream
2
ASF 1096 placebo cream
Interventions
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ASF 1096 0.5 % cream
ASF 1096 placebo cream
Eligibility Criteria
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Inclusion Criteria
* Histological results from biopsy confirming the diagnosis (biopsy can be taken at screening)
* Is prepared to grant authorised persons access to the medical records
* Has signed informed consent
Exclusion Criteria
* Has scarring at the target lesion
* Systemic treatment of SLE
18 Years
70 Years
ALL
No
Sponsors
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Astion Pharma A/S
INDUSTRY
Locations
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Gregor Jemec
Roskilde Hospital, , Denmark
Countries
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Other Identifiers
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ASF1096-203
Identifier Type: -
Identifier Source: org_study_id