Overview

TRUST Study: Raptiva ® in Hand & Foot Psoriasis

Status:
Terminated
Trial end date:
2009-06-01
Target enrollment:
Participant gender:
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).
Phase:
Phase 4
Details
Lead Sponsor:
Merck KGaA
Merck KGaA, Darmstadt, Germany
Treatments:
Antibodies
Antibodies, Monoclonal