Clinical Trials Directory

Trials / Completed

CompletedNCT00256139

CLEAR Study: Clinical Experience Acquired With Raptiva Study

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
793 (actual)
Sponsor
Merck KGaA, Darmstadt, Germany · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers

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

Conditions

Interventions

TypeNameDescription
DRUGRaptiva

Timeline

Start date
2003-03-01
Primary completion
2004-10-01
Completion
2004-10-01
First posted
2005-11-21
Last updated
2017-01-16

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT00256139. Inclusion in this directory is not an endorsement.

CLEAR Study: Clinical Experience Acquired With Raptiva Study (NCT00256139) · Clinical Trials Directory