Viewing Study NCT01806597



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Last Modification Date: 2024-10-26 @ 11:04 AM
Study NCT ID: NCT01806597
Status: COMPLETED
Last Update Posted: 2018-02-22
First Post: 2013-01-23

Brief Title: Study of Safety Tolerability and Efficacy of Secukinumab in Subjects With Moderate to Severe Palmoplantar Psoriasis
Sponsor: Novartis Pharmaceuticals
Organization: Novartis

Study Overview

Official Title: A Randomized Double-blind Placebo-controlled Multicenter Study to Demonstrate the Efficacy at 16 Weeks of Secukinumab 150 and 300 mg sc and to Assess Safety Tolerability and Long-term Efficacy up to 132 Weeks in Subjects With Moderate to Severe Palmoplantar Psoriasis
Status: COMPLETED
Status Verified Date: 2018-01
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: GESTURE
Brief Summary: Purpose of the study was to demonstrate the efficacy of secukinumab versus placebo on palmoplantar psoriasis and to assess the long term efficacy safety and tolerability of secukinumab
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
2012-005412-25 EUDRACT_NUMBER None None