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Completed Phase 3 Interventional Results available

Effect of Secukinumab on Radiographic Progression in Ankylosing Spondylitis as Compared to GP2017 (Adalimumab Biosimilar)

ClinicalTrials.gov ID: NCT03259074

Public ClinicalTrials.gov record NCT03259074. 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 25, 2026, 5:36 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, Partially-blinded Study of Secukinumab to Demonstrate Reduction of Radiographic Progression Versus GP2017 (Adalimumab Biosimilar) at 104 Weeks and to Assess the Long Term Safety, Tolerability and Efficacy up to 2 Years in Patients With Active Ankylosing Spondylitis

Brief summary

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

The purpose of this study is to demonstrate the impact of secukinumab on the progression of structural damage in the spine, as measured by the modified Stoke Ankylosing Spondylitis Spine Score (mSASSS) in patients with Ankylosing Spondylitis (AS).

Study identification

NCT ID
NCT03259074
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
859 participants

Conditions and interventions

Interventions

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
Nov 30, 2017 (Actual)
Primary completion
Nov 12, 2021 (Actual)
Completion
Nov 29, 2021 (Actual)
Last update posted
Aug 21, 2023

2017 – 2021

United States locations

U.S. sites
19
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Novartis Investigative Site Mesa Arizona 85202 —
Novartis Investigative Site Escondido California 92025 —
Novartis Investigative Site La Mesa California 91942 —
Novartis Investigative Site San Francisco California 94143 0138 —
Novartis Investigative Site Gainesville Florida 32607 —
Novartis Investigative Site Boise Idaho 83702 —
Novartis Investigative Site Shreveport Louisiana 71101 —
Novartis Investigative Site Wheaton Maryland 20902 —
Novartis Investigative Site Great Falls Montana 59405 —
Novartis Investigative Site Lincoln Nebraska 68516 —
Novartis Investigative Site Greensboro North Carolina 27408 —
Novartis Investigative Site Dayton Ohio 45402 —
Novartis Investigative Site Middleburg Heights Ohio 44130 —
Novartis Investigative Site Portland Oregon 97239 —
Novartis Investigative Site Duncansville Pennsylvania 16635 —
Novartis Investigative Site Memphis Tennessee 38119 —
Novartis Investigative Site Mesquite Texas 75150 —
Novartis Investigative Site Kennewick Washington 99336 —
Novartis Investigative Site Franklin Wisconsin 53132 —

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 152 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03259074, 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 21, 2023 · Synced Oct 25, 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 public registry record, listed eligibility criteria, and available contact information for NCT03259074 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →