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Terminated Phase 3 Interventional Results available

Secukinumab Efficacy and Safety Study in Patients With Rheumatoid Arthritis and Inadequate Response to Anti-TNFα Agents.

ClinicalTrials.gov ID: NCT01770379

Public ClinicalTrials.gov record NCT01770379. 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 Jul 22, 2026, 4:31 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 Phase III Randomized, Double-blind, Placebo-controlled Multicenter Study of Subcutaneous Secukinumab in Prefilled Syringes to Demonstrate the Efficacy at 24 Weeks and to Assess the Long Term Efficacy, Safety, Tolerability and Usability up to 5 Years in Patients With Active Rheumatoid Arthritis Who Have an Inadequate Response to Anti-TNFα Agents

Study identification

NCT ID
NCT01770379
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
242 participants

Conditions and interventions

Interventions

  • Secukinumab (AIN457) Biological
  • Placebo Biological

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
Sep 30, 2012
Primary completion
Apr 30, 2015
Completion
Apr 30, 2015
Last update posted
Jul 20, 2016

2012 – 2015

United States locations

U.S. sites
25
U.S. states
15
U.S. cities
23
Facility City State ZIP Site status
Novartis Investigative Site Peoria Arizona 85381
Novartis Investigative Site Santa Monica California 90404
Novartis Investigative Site Upland California 91786
Novartis Investigative Site Miami Florida 33135
Novartis Investigative Site Pembroke Pines Florida 33026
Novartis Investigative Site Zephyrhills Florida 33542
Novartis Investigative Site Cumberland Maryland 21502
Novartis Investigative Site Edina Minnesota 55435
Novartis Investigative Site Tupelo Mississippi 38801
Novartis Investigative Site Lees Summit Missouri 64086
Novartis Investigative Site St Louis Missouri 63128
Novartis Investigative Site Reno Nevada 89502
Novartis Investigative Site Albuquerque New Mexico 87102
Novartis Investigative Site Zanesville Ohio 43701
Novartis Investigative Site Oklahoma City Oklahoma 73103
Novartis Investigative Site Oklahoma City Oklahoma 73134
Novartis Investigative Site North Charleston South Carolina 29406
Novartis Investigative Site Rapid City South Dakota 57701
Novartis Investigative Site Jackson Tennessee 38305
Novartis Investigative Site Nashville Tennessee 37203-1424
Novartis Investigative Site Amarillo Texas 79124
Novartis Investigative Site Benbrook Texas 76126
Novartis Investigative Site Houston Texas 77005
Novartis Investigative Site Houston Texas 77034
Novartis Investigative Site Mesquite Texas 75150

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 52 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01770379, 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 Jul 20, 2016 · Synced Jul 22, 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 NCT01770379 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →