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Completed Phase 2 Interventional Results available

A Biomarker Study of Secukinumab in Rheumatoid Arthritis (RA) Patients

ClinicalTrials.gov ID: NCT01426789

Public ClinicalTrials.gov record NCT01426789. 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 21, 2026, 9:55 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 Multicenter, 12 Week, Randomized, Double-blind, Placebo-controlled Biomarker Study of Secukinumab (AIN457) in Rheumatoid Arthritis Patients Followed by an Open Label Extension

Brief summary

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

This study aims to confirm if patients with a specific biomarker might have a better response to secukinumab treatment. To meet this purpose, exploratory biomarker studies will be done. The goals of these exploratory studies are to (1) find biomarkers that will identify persons with rheumatoid arthritis who will have the best possible response to secukinumab and (2) to identify persons who will have fewer side effects in order to maximize their benefit from secukinumab.

Study identification

NCT ID
NCT01426789
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
100 participants

Conditions and interventions

Interventions

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 2011 (Type not available)
Primary completion
Feb 2014 (Actual)
Completion
Feb 2014 (Actual)
Last update posted
Aug 10, 2015

2011 – 2014

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
Novartis Investigative Site Phoenix Arizona 85023 —
Novartis Investigative Site Tuscon Arizona 85724 —
Novartis Investigative Site Anahiem California 92804 —
Novartis Investigative Site Clearwater Florida 33756 —
Novartis Investigative Site Coral Gables Florida 33134 —
Novartis Investigative Site Fleming Island Florida 32003 —
Novartis Investigative Site Miami Florida 33143 —
Novartis Investigative Site Pinellas Park Florida 33781 —
Novartis Investigative Site Venice Florida 34292 —
Novartis Investigative Site Marietta Georgia 30060 —
Novartis Investigative Site South Bend Indiana 46601 —
Novartis Investigative Site Springfield Missouri 65807 —
Novartis Investigative Site Albuquerque New Mexico 87102 —
Novartis Investigative Site Statesville North Carolina 28625 —
Novartis Investigative Site Oklahoma City Oklahoma 73112 —
Novartis Investigative Site San Antonio Texas 78217 —

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01426789, 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 Aug 10, 2015 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01426789 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →