Clinical Trials Directory

Trials / Completed

CompletedNCT00216840

Efficacy and Safety of Calcipotriol Plus Betamethasone Dipropionate Gel in Scalp Psoriasis

Calcipotriol Plus Betamethasone Dipropionate Gel Compared to Betamethasone Dipropionate in the Gel Vehicle and Calcipotriol in the Gel Vehicle in Scalp Psoriasis

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
1,350 (planned)
Sponsor
LEO Pharma · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to evaluate whether once daily topical treatment for up to 8 weeks of calcipotriol 50 mcg/g plus betamethasone 0.5 mg/g (as dipropionate) gel is safe and more effective than betamethasone 0.5 mg/g (as dipropionate) in the gel vehicle and calcipotriol 50 mcg/g in the gel vehicle in patients with scalp psoriasis. The primary response criterion is the number of patients with absence of disease and very mild disease after 8 weeks of treatment.

Conditions

Interventions

TypeNameDescription
DRUGCalcipotriol plus betamethasone dipropionate (LEO80185 gel)

Timeline

Start date
2004-12-01
Completion
2005-09-01
First posted
2005-09-22
Last updated
2025-02-24

Locations

7 sites across 7 countries: Belgium, Canada, Finland, France, Germany, Netherlands, United Kingdom

Source: ClinicalTrials.gov record NCT00216840. Inclusion in this directory is not an endorsement.