ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Efficacy at 24 Weeks and Long Term Safety, Tolerability and Efficacy up to 2 Years of Secukinumab (AIN457) in Patients With Active Psoriatic Arthritis (PsA)

ClinicalTrials.gov ID: NCT01392326

Public ClinicalTrials.gov record NCT01392326. 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 7, 2026, 12:11 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, Multicenter Study of Secukinumab to Demonstrate the Efficacy at 24 Weeks and to Assess the Long Term Safety, Tolerability and Efficacy up to 2 Years in Patients With Active Psoriatic Arthritis

Study identification

NCT ID
NCT01392326
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
606 participants

Conditions and interventions

Interventions

  • Placebo Comparator Drug
  • Secukinumab (150 mg) Drug
  • Secukinumab (75 mg) Drug

Drug

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
Aug 31, 2011
Primary completion
Sep 30, 2014
Completion
Sep 30, 2014
Last update posted
Feb 3, 2016

2011 – 2014

United States locations

U.S. sites
25
U.S. states
18
U.S. cities
23
Facility City State ZIP Site status
Novartis Investigative Site Anniston Alabama 36207-5710
Novartis Investigative Site Mesa Arizona 85202
Novartis Investigative Site Paradise Valley Arizona 85253
Novartis Investigative Site Upland California 91786
Novartis Investigative Site Tamarac Florida 33321
Novartis Investigative Site Newnan Georgia 30263
Novartis Investigative Site Boston Massachusetts 02111
Novartis Investigative Site Eagan Minnesota 55121
Novartis Investigative Site Richmond Heights Missouri 63117
Novartis Investigative Site Lincoln Nebraska 68516
Novartis Investigative Site Freehold New Jersey 07728
Novartis Investigative Site Charlotte North Carolina 28210
Novartis Investigative Site Oklahoma City Oklahoma 73103
Novartis Investigative Site Duncansville Pennsylvania 16635
Novartis Investigative Site Johnston Rhode Island 02919
Novartis Investigative Site Columbia South Carolina 29204
Novartis Investigative Site North Charleston South Carolina 29406
Novartis Investigative Site Jackson Tennessee 38305
Novartis Investigative Site Benbrook Texas 76126
Novartis Investigative Site Dallas Texas 75216
Novartis Investigative Site Dallas Texas 75246
Novartis Investigative Site Houston Texas 77034
Novartis Investigative Site Houston Texas 77074
Novartis Investigative Site Mesquite Texas 75150
Novartis Investigative Site Seattle Washington 98122

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 85 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01392326, 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 Feb 3, 2016 · Synced May 7, 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 NCT01392326 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →