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Discoid Lupus Erythematosus

A Phase 2, pilot, multicenter, randomized, placebo-controlled sequential, ascending dose study to
characterize the safety, tolerability, pharmacokinetic and pharmacodynamic activity of CC-930 in subjects with recalcitrant Discoid Lupus Erythematosus (DLE).


The purpose of the study is to assess if CC-930 is safe and tolerable in treating subjects with
Discoid Lupus Erythematosus. Pharmacokinetic and pharmacodynamics will also be evaluated.



contact information:
Nicole Bisby or visit www.clinicaltrials.gov (Reference # NCT01466725) 202.741.2437
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