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Completed Phase 3 Interventional Results available

Study to Demonstrate the Efficacy, Safety and Tolerability of Intravenous Secukinumab up to 52 Weeks in Subjects With Active Psoriatic Arthritis

ClinicalTrials.gov ID: NCT04209205

Public ClinicalTrials.gov record NCT04209205. 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 May 12, 2026, 6:37 AM 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, Phase III Multicenter Study of Intravenous Secukinumab to Compare Efficacy at 16 Weeks With Placebo and to Assess Safety and Tolerability up to 52 Weeks in Subjects With Active Psoriatic Arthritis

Study identification

NCT ID
NCT04209205
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
381 participants

Conditions and interventions

Interventions

  • AIN457 3 mg/kg Drug
  • AIN457 6 mg/kg i.v. Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 100 Years
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
Jan 28, 2020
Primary completion
May 16, 2022
Completion
May 16, 2022
Last update posted
May 15, 2025

2020 – 2022

United States locations

U.S. sites
31
U.S. states
18
U.S. cities
31
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35205
Novartis Investigative Site Fountain Valley California 92708
Novartis Investigative Site Fullerton California 92835
Novartis Investigative Site La Mesa California 91942
Novartis Investigative Site Santa Monica California 90404
Novartis Investigative Site Upland California 91786
Novartis Investigative Site Van Nuys California 91405
Novartis Investigative Site West Hills California 91307
Novartis Investigative Site Denver Colorado 80230
Novartis Investigative Site Clearwater Florida 33765
Novartis Investigative Site Miami Florida 33032
Novartis Investigative Site Ocoee Florida 34761
Novartis Investigative Site Plantation Florida 33324
Novartis Investigative Site Tampa Florida 33624
Novartis Investigative Site Winter Park Florida 32789
Novartis Investigative Site Marietta Georgia 30060
Novartis Investigative Site Indianapolis Indiana 46256
Novartis Investigative Site Bowling Green Kentucky 42101
Novartis Investigative Site St Louis Missouri 63117
Novartis Investigative Site Lincoln Nebraska 68516
Novartis Investigative Site Voorhees Township New Jersey 08043
Novartis Investigative Site Rochester New York 14642
Novartis Investigative Site Greensboro North Carolina 27408
Novartis Investigative Site Middleburg Heights Ohio 44130
Novartis Investigative Site Oklahoma City Oklahoma 73103
Novartis Investigative Site Tulsa Oklahoma 74136
Novartis Investigative Site Duncansville Pennsylvania 16635
Novartis Investigative Site Jackson Tennessee 38305
Novartis Investigative Site Austin Texas 78731
Novartis Investigative Site Mesquite Texas 75150
Novartis Investigative Site Newport News Virginia 23608

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 49 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04209205, 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 May 15, 2025 · Synced May 12, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04209205 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →