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Completed Phase 3 Interventional Results available

Study of Efficacy and Safety of Secukinumab in Patients With Non-radiographic Axial Spondyloarthritis

ClinicalTrials.gov ID: NCT02696031

Public ClinicalTrials.gov record NCT02696031. 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 26, 2026, 2:13 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 150 mg in Patients With Active nr- axSpA to Evaluate the Safety,Tolerability and Efficacy up to 2 Yrs, Followed by an Opt Phase of Either 150 mg or 300 mg Randomized Dose Escalation for up to Another 2 Yrs

Brief summary

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

The purpose of this study was to demonstrate the clinical efficacy, safety and tolerability of secukinumab compared to placebo in patients with nr-axSpA at Week 16 as well as Week 52 and long term efficacy and safety up to Week 104 (core phase) followed by an optional extension phase consisting of a 16-week randomized dose escalation treatment period and a continuous treatment period for up to Week 208

Study identification

NCT ID
NCT02696031
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
555 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
Apr 29, 2016 (Actual)
Primary completion
Jul 1, 2019 (Actual)
Completion
Mar 11, 2021 (Actual)
Last update posted
Apr 29, 2022

2016 – 2021

United States locations

U.S. sites
18
U.S. states
15
U.S. cities
18
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35205 —
Novartis Investigative Site Beverly Hills California 90211 —
Novartis Investigative Site Fullerton California 92835 —
Novartis Investigative Site Denver Colorado 80230 —
Novartis Investigative Site Gainesville Florida 32608 —
Novartis Investigative Site Idaho Falls Idaho 83404 —
Novartis Investigative Site Bowling Green Kentucky 42101 —
Novartis Investigative Site Lansing Michigan 48910 —
Novartis Investigative Site Great Falls Montana 59405 —
Novartis Investigative Site Albany New York 12206 —
Novartis Investigative Site Potsdam New York 13676 —
Novartis Investigative Site Charlotte North Carolina 28204 —
Novartis Investigative Site Oklahoma City Oklahoma 73102 —
Novartis Investigative Site Portland Oregon 97239 —
Novartis Investigative Site Duncansville Pennsylvania 16635 —
Novartis Investigative Site Charleston South Carolina 29460 —
Novartis Investigative Site Leander Texas 78641 —
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 121 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02696031, 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 Apr 29, 2022 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02696031 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →