drugset / Trial / NCT00096980

A Study to Evaluate Raptiva in Combination With Topical Psoriasis Therapies

NCT00096980

Phase 4 Completed 300 enrolled Genentech, Inc.
RandomizedOpen-labelTreatment

Summary

This study is an open label, randomized, multicenter study designed to compare the efficacy of 12 weeks of subcutaneously administered efalizumab (monotherapy) with that of combination therapy (Efalizumab and a topical corticosteroid ointment) in subjects with moderate to severe plaque psoriasis who are candidates for systemic therapy. The study will also evaluate the safety and tolerability of 30 months of continuous efalizumab treatment in those subjects who derive benefit from the initial 12 weeks of treatment.

Timeline

Start
2001-02
Primary completion
Completion
2004-05

Drugs

EvaluationDrugModalityDoseRoute
Subject efalizumab Monoclonal antibody Subcutaneous

Indications