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Trials / Completed

CompletedNCT01120223

Safety and Efficacy of LEO 80185 Gel in Adolescent Subjects (Aged 12 to 17) With Scalp Psoriasis

Safety and Efficacy of Calcipotriol Plus Betamethasone Dipropionate Gel in Adolescent Subjects (Aged 12 to 17) With Scalp Psoriasis

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
78 (actual)
Sponsor
LEO Pharma · Industry
Sex
All
Age
12 Years – 17 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to evaluate the safety and efficacy of once daily use of LEO 80185 gel in adolescent subjects (aged 12 to 17) with scalp psoriasis. LEO 80185 gel has marketing approval in many countries under the brand names Xamiol® gel and Taclonex Scalp® Topical Suspension for the treatment of scalp psoriasis in adults. No studies have been performed in subjects younger than 18 years

Conditions

Interventions

TypeNameDescription
DRUGLEO 80185 (Xamiol® gel/Taclonex® Scalp topical suspension)Once daily application

Timeline

Start date
2010-05-01
Primary completion
2012-08-01
Completion
2012-10-01
First posted
2010-05-10
Last updated
2025-03-11
Results posted
2014-12-01

Locations

17 sites across 3 countries: Canada, France, United Kingdom

Source: ClinicalTrials.gov record NCT01120223. Inclusion in this directory is not an endorsement.

Safety and Efficacy of LEO 80185 Gel in Adolescent Subjects (Aged 12 to 17) With Scalp Psoriasis (NCT01120223) · Clinical Trials Directory