SLE / CLE
Estado: ReclutandoA Phase II, Randomized, Double-Blind, Placebo-Controlled Dose-Ranging, Parallel and Adaptive Study to Evaluate the Efficacy and Safety of Enpatoran in Systemic Lupus Erythematosus and in Cutaneous Lupus Erythematosus (Subacute Cutaneous Lupus Erythematosus and/or Discoid Lupus Erythematosus) Participants Receiving Standard of Care.
Para inscribirte contáctate a:
[email protected]
Principales Criterios de Inclusión:
- Are ≥ 18 to ≤ 75 years of age at the time of signing the informed consent.
- Diagnosis of SCLE or DLE documented in medical history. Predominant findings of active lupus rash must be SCLE and/or DLE, but other skin manifestations of CLE will be allowed (e.g., lupus tumidus, Acute Cutaneous Lupus Erythematosus [ACLE], etc) on a case-by-case basis if their main diagnosis is active SCLE and/or DLE.
- Disease duration of ≥ 6 months from time of diagnosis to Screening.
- CLASI-A ≥ 8 at Screening Visit; this must be confirmed at Day 1 Visit.
- Laboratorio:Merck
- Área Terapéutica:
- Fase del estudio:II
- Código de Estudio:MS200569_0003
- Ver ensayo en Clinical Trials
Santiago
- Clínica Dermacross
Santiago
- PROSALUD
Santiago
- Biomedica Research Group
Santiago
- Centro Internacional de Estudios Clínicos
Santiago
- CECIM
Osorno
- Clínica Alemana de Osorno
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