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Trials / Completed

CompletedNCT00437255

Efficacy, Safety, Preference and Response Duration of Clobex® Spray and Taclonex® Ointment in Psoriasis

An Evaluation of the Efficacy, Safety, Preference and Duration of Response of Clobex® (Clobetasol Propionate) Spray and Taclonex® (Calcipotriene 0.05%/Betamethasone Dipropionate 0.064%) Ointment in Subjects With Stable Plaque Psoriasis

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
122 (actual)
Sponsor
Galderma R&D · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Evaluate the efficacy of Clobex® Spray as compared to Taclonex® Ointment in terms of Overall Disease Severity and Investigator Global Assessment.

Detailed description

Same as above.

Conditions

Interventions

TypeNameDescription
DRUGClobetasol Propionate, 0.05%Topical, twice daily for 4 weeks
DRUGCalcipotriene and betamethasone dipropionate ointmentTopical, once daily

Timeline

Start date
2006-08-01
Primary completion
2007-06-01
Completion
2007-06-01
First posted
2007-02-19
Last updated
2022-07-29

Locations

4 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00437255. Inclusion in this directory is not an endorsement.

Efficacy, Safety, Preference and Response Duration of Clobex® Spray and Taclonex® Ointment in Psoriasis (NCT00437255) · Clinical Trials Directory