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
| Type | Name | Description |
|---|---|---|
| DRUG | Calcipotriol 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.