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Completed Phase 4 Interventional Results available

Study to Explore the Effect of Secukinumab, Compared to Placebo, on Fat Tissue and Skin in Plaque Psoriasis Patients

ClinicalTrials.gov ID: NCT03055494

Public ClinicalTrials.gov record NCT03055494. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 25, 2026, 1:25 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Explore Changes in Subcutaneous Adipose Tissue and Modulation of Skin Inflammation After 12 Weeks of Treatment With Secukinumab, Compared to Placebo, and up to 52 Weeks of Treatment With Secukinumab in Adult Patients With Moderate to Severe Plaque Psoriasis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study provided a comparison of secukinumab to placebo with respect to skin inflammation as measured by skin exams in comparison to skin biopsies, adipose tissue and blood sample analyses.

Study identification

NCT ID
NCT03055494
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
102 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 18, 2017 (Actual)
Primary completion
Apr 25, 2018 (Actual)
Completion
Feb 26, 2019 (Actual)
Last update posted
Mar 10, 2023

2017 – 2019

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Novartis Investigative Site Hot Springs Arkansas 71913 —
Novartis Investigative Site Los Angeles California 90033 —
Novartis Investigative Site Santa Ana California 92701 —
Novartis Investigative Site Atlanta Georgia 30342 —
Novartis Investigative Site Indianapolis Indiana 46256 —
Novartis Investigative Site East Windsor New Jersey 08520 —
Novartis Investigative Site West Orange New Jersey 07052 —
Novartis Investigative Site Buffalo New York 14203 —
Novartis Investigative Site New York New York 10025 1737 —
Novartis Investigative Site New York New York 10065 —
Novartis Investigative Site Portland Oregon 97223 —
Novartis Investigative Site Pittsburgh Pennsylvania 15213-3403 —
Novartis Investigative Site Webster Texas 77004 —
Novartis Investigative Site Murray Utah 84107 —
Novartis Investigative Site Norfolk Virginia 23507 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03055494, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 10, 2023 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03055494 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →