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
| Type | Name | Description |
|---|---|---|
| DRUG | Clobetasol Propionate, 0.05% | Topical, twice daily for 4 weeks |
| DRUG | Calcipotriene and betamethasone dipropionate ointment | Topical, 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.