drugset / Trial / NCT00256139

CLEAR Study: Clinical Experience Acquired With Raptiva Study

NCT00256139

Phase 3 Completed 793 enrolled Merck KGaA, Darmstadt, Germany
RandomizedParallel-groupDouble-blindTreatment

Summary

A multicentre, randomised, double blind, placebo controlled phase III study of subcutaneously administered Raptiva in the treatment of patients with moderate to severe psoriasis

Timeline

Start
2003-03
Primary completion
2004-10
Completion
2004-10

Drugs

EvaluationDrugModalityDoseRoute
Subject efalizumab Monoclonal antibody 1 mg/kg Subcutaneous

Indications