drugset / Trial / NCT00739882

TRUST Study: Raptiva ® in Hand & Foot Psoriasis

NCT00739882

Phase 4 Terminated 76 enrolled Merck KGaA, Darmstadt, Germany
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To evaluate the safety and efficacy of Raptiva ® compared with placebo to control chronic moderate to severe plaque psoriasis involving the hands and/or feet scoring Physician's Global Assessment (PGA - H\&F) greater-than or equal to 3 in subjects not suitable for other systemic therapies including cyclosporine, methotrexate, and Psoralen-Ultraviolet Light A (PUVA).

Timeline

Start
2008-04
Primary completion
2009-06
Completion
2009-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator efalizumab Monoclonal antibody 1 mg/kg

Indications