Investigaciones Clinicas Tucuman | San Miguel de Tucuman, Argentina
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The purpose of the study is to evaluate the long term safety and efficacy of orally administered M5049 in participants with subacute cutaneous lupus erythematosus (SCLE), discoid lupus erythematosus (DLE) and/or systemic lupus erythematosus (SLE) who have completed the 24 week treatment period of Willow study (MS200569_0003 [NCT05162586]).
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532 participants in 4 patient groups
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Data sourced from clinicaltrials.gov
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