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A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Comparison Study of CC-10004 in Subjects with Moderate-to-severe Plaque-Type Psoriasis

Mise à jour : Il y a 4 ans
Référence : EUCTR2006-000057-22

Femme et Homme

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Extrait

To compare the clinical efficacy of 2 oral (PO) doses of CC-10004 (20 mg once daily (QD) and 20 mg twice daily (BID)) with placebo when taken for 12 weeks in subjects with moderate-to-severe plaque-type psoriasis

Critère d'inclusion

  • Moderate to severe plaque-type psoriasis

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