Viewing Study NCT00437619



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Last Modification Date: 2024-10-26 @ 9:31 AM
Study NCT ID: NCT00437619
Status: COMPLETED
Last Update Posted: 2015-12-02
First Post: 2007-02-19

Brief Title: A Study of Sequential Treatment With Daivobet Betamethasone Dipropionate Plus Calcipotriol and Daivonex Calcipotriol in Patients With Psoriasis
Sponsor: Hoffmann-La Roche
Organization: Hoffmann-La Roche

Study Overview

Official Title: An Open Label Study to Evaluate the Clinical Response to Sequential Treatment With Daivobet and Daivonex in Patients With Mild to Moderate Psoriasis
Status: COMPLETED
Status Verified Date: 2015-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This single arm study will evaluate the efficacy and safety of sequential treatment with Diavobet betamethasone propionate 05mgg plus calcipotriol hydrate 50 microgramsg once daily for 4 weeks followed by Daivonex calcipotriol hydrate 50 microgramsg twice daily for 4 weeks in the control of signs and symptoms in patients with mild to moderate psoriasis Only patients showing a 50 response to Daivobet will progress to the Daivonex maintenance phase The anticipated time on study treatment is 3 months and the target sample size is 100-500 individuals
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None