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]).
Condition | Systemic Lupus Erythematosus |
---|---|
Treatment | Placebo, M5049 low dose, M5049 medium dose, M5049 high dose, M5049 very high dose |
Clinical Study Identifier | NCT05540327 |
Sponsor | Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany |
Last Modified on | 20 September 2023 |
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