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Efficacy of Topical Tacrolimus in Different Subtypes With Cutaneous Lupus Erythematosus (CLE) - Trial NCT00317681

Access comprehensive clinical trial information for NCT00317681 through Pure Global AI's free database. This Phase 2 trial is sponsored by Heinrich-Heine University, Duesseldorf and is currently Completed. The study focuses on Cutaneous Lupus Erythematosus. Target enrollment is 30 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT00317681
Phase 2
Completed
drug
Trial Details
ClinicalTrials.gov โ€ข NCT00317681
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Efficacy of Topical Tacrolimus in Different Subtypes With Cutaneous Lupus Erythematosus (CLE)
The Efficacy of Topical Tacrolimus in the Treatment of Cutaneous Lupus Erythematosus - a Multi-Center-Trial

Study Focus

Tacrolimus ointment

Interventional

drug

Sponsor & Location

Heinrich-Heine University, Duesseldorf

Duesseldorf, Germany

Timeline & Enrollment

Phase 2

Aug 01, 2005

Feb 01, 2007

30 participants

Primary Outcome

Difference in skin lesions of patients with CLE before (begin of study) and after treatment (end of study) evaluated by a clinical score

Summary

The purpose of this study is to evaluate the efficacy of topical tacrolimus in different
 subtypes of cutaneous lupus erythematosus. As shown by several groups activated memory T
 lymphocytes play a key role in the pathogenesis of lupus erythematosus. Tacrolimus targets T
 lymphocytes and suppresses their activation by inhibiting the expression of cytokine genes,
 such as IL-2. Therefore, treatment of cutaneous lupus erythematosus with topical tacrolimus
 might result in an improvement of skin lesions in such patients.

ICD-10 Classifications

Subacute cutaneous lupus erythematosus
Lupus erythematosus
Discoid lupus erythematosus
Systemic lupus erythematosus
Systemic lupus erythematosus, unspecified

Data Source

ClinicalTrials.gov

NCT00317681

Non-Device Trial