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Completed Phase 3 Interventional Results available

Efficacy and Safety of 2 Secukinumab Regimens in 90kg or More Weight Group With Moderate/Severe Chronic Plaque Psoriasis

ClinicalTrials.gov ID: NCT03504852

Public ClinicalTrials.gov record NCT03504852. 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 24, 2026, 12:36 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, Multicenter Study Assessing Short and Long-term Efficacy, Safety, and Tolerability of Sub-cutaneous Secukinumab in Subjects of Body Weight 90 kg or Higher With Moderate to Severe Chronic Plaque-type Psoriasis

Brief summary

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

The purpose of this study is to assess secukinumab high dose (every 2 weeks) vs standard dose (every 4 weeks) in heavy body weight subjects with moderate to severe plaque psoriasis.

Study identification

NCT ID
NCT03504852
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
331 participants

Conditions and interventions

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
Jun 25, 2018 (Actual)
Primary completion
Sep 13, 2019 (Actual)
Completion
Jul 15, 2020 (Actual)
Last update posted
Oct 11, 2021

2018 – 2020

United States locations

U.S. sites
38
U.S. states
23
U.S. cities
37
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35205 —
Novartis Investigative Site Phoenix Arizona 85032 —
Novartis Investigative Site Rogers Arkansas 72758 —
Novartis Investigative Site Irvine California 92697 —
Novartis Investigative Site Sacramento California 95817 —
Novartis Investigative Site Sacramento California 95819 —
Novartis Investigative Site San Diego California 92123 —
Novartis Investigative Site Santa Monica California 90404 —
Novartis Investigative Site Centennial Colorado 80111 —
Novartis Investigative Site Tampa Florida 33612 —
Novartis Investigative Site West Palm Beach Florida 33409 —
Novartis Investigative Site Alpharetta Georgia 30022 —
Novartis Investigative Site Snellville Georgia 30078 —
Novartis Investigative Site Skokie Illinois 60077 —
Novartis Investigative Site Indianapolis Indiana 46256 —
Novartis Investigative Site New Albany Indiana 47150 —
Novartis Investigative Site Louisville Kentucky 40241 —
Novartis Investigative Site Owensboro Kentucky 42303 —
Novartis Investigative Site Boston Massachusetts 02111 —
Novartis Investigative Site New Brighton Minnesota 55112 —
Novartis Investigative Site Saint Joseph Missouri 64506 —
Novartis Investigative Site East Windsor New Jersey 08520 —
Novartis Investigative Site Verona New Jersey 07044 —
Novartis Investigative Site Forest Hills New York 11375 —
Novartis Investigative Site New York New York 10025 1737 —
Novartis Investigative Site Charlotte North Carolina 28277 —
Novartis Investigative Site Winston-Salem North Carolina 27157 —
Novartis Investigative Site Fairborn Ohio 45324 —
Novartis Investigative Site Oregon City Oregon 97045 —
Novartis Investigative Site Portland Oregon 97210 —
Novartis Investigative Site Charleston South Carolina 29414 —
Novartis Investigative Site Houston Texas 77056 —
Novartis Investigative Site Mesquite Texas 75150 —
Novartis Investigative Site Pflugerville Texas 78660 —
Novartis Investigative Site San Antonio Texas 78218 —
Novartis Investigative Site Norfolk Virginia 23507 —
Novartis Investigative Site Wenatchee Washington 98801 —
Novartis Investigative Site Madison Wisconsin 53717 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03504852, 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 Oct 11, 2021 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03504852 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →