drugset / Trial / NCT00263718

Efficacy and Safety of Calcipotriol Plus Betamethasone Dipropionate Gel in Psoriasis Vulgaris

NCT00263718

Phase 2 Completed 360 enrolled LEO Pharma
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective of the study is to compare the use of calcipotriol plus betamethasone dipropionate gel with betamethasone dipropionate in the gel vehicle, calcipotriol in the gel vehicle and the gel vehicle alone when used in patients with psoriasis vulgaris on the trunk and/or limbs. Patients will be treated once daily for up to 8 weeks. The primary response criterion is the number of patients with controlled disease at week 8.

Timeline

Start
2005-12
Primary completion
Completion
2006-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Calcipotriol Small molecule
Subject betamethasone dipropionate Small molecule

Indications