Clinical Trials Directory

Trials / Completed

CompletedNCT01083758

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

Effect of Calcipotriol Plus Betamethasone Dipropionate Topical Suspension on the HPA Axis and Calcium Metabolism in Adolescent Subjects (Aged 12 to 17 Years) With Scalp Psoriasis

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
31 (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 topical suspension in adolescent subjects (aged 12 to 17 years) with scalp psoriasis. LEO 80185 topical suspension has marketing approval in many countries under the brand names Taclonex Scalp® Topical Suspension and Xamiol® gel for the treatment of scalp psoriasis in adults. No studies have been performed in subjects younger than 18 years.

Conditions

Interventions

TypeNameDescription
DRUGLEO 80185 (Taclonex® Scalp topical suspension/Xamiol® gel)Topical suspension applied once daily for up to 8 weeks

Timeline

Start date
2010-04-01
Primary completion
2012-08-01
Completion
2012-10-01
First posted
2010-03-10
Last updated
2025-03-11
Results posted
2015-10-12

Locations

6 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01083758. Inclusion in this directory is not an endorsement.