Overview

A Study to Evaluate the Safety of Raptiva in Adults With Plaque Psoriasis Previously Enrolled in Study ACD2600g

Status:
Completed
Trial end date:
2004-07-01
Target enrollment:
Participant gender:
Summary
This is an open label, multicenter study designed to evaluate the safety and tolerability of efalizumab administered subcutaneously at weekly doses of 1.0 mg/kg in subjects with plaque psoriasis who previously participated in Study ACD2600g.
Phase:
Phase 3
Details
Lead Sponsor:
Genentech, Inc.