CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 20 enrolled
Drug / intervention
Secukinumab +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03041038
NCT03041038Phase 2Completed

A Multicenter Study With a Randomized, Double-Blind, Placebo-Controlled Period, Followed by an Open-Label Maintenance Dosing Period to Evaluate the Efficacy and Safety of Secukinumab in Patients With Ichthyoses

Northwestern University·interventional·Posted Feb 2, 2017·Updated Aug 25, 2021

In Brief

A Phase 2 clinical trial evaluating Secukinumab and Placebo for Ichthyosis and 5 related conditions. Completed, enrolled 20 participants across 2 sites.

Detailed Summary

The ichthyoses are a group of lifelong genetic disorders which share characteristics of generalized skin thickening, scaling and underlying cutaneous inflammation. There are no therapies based on growing understanding of what causes the disease. However, there have been recent discoveries of marked elevations in expression of interleukin-17A (IL-17A) and IL-17-related cytokines in the skin of individuals with ichthyosis, which may explain the inflammation. Investigators propose that IL-17-targeting therapeutics will safely suppress the inflammation and possibly the other features of ichthyosis, improving quality of life.

Study Details

Timeline

Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedFeb 2, 2017
Enrollment StartDec 1, 2016
Primary CompletionAug 31, 2020
TodayJul 2, 2026
Enrollment to primary: 3.8 yearsPosted 9.4 years ago

Interventions

Secukinumabdrug

Anti IL-17A antibody

Placebodrug