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Completed Phase 3 Interventional Results available

Efficacy of Secukinumab Compared to Adalimumab in Patients With Psoriatic Arthritis

ClinicalTrials.gov ID: NCT02745080

Public ClinicalTrials.gov record NCT02745080. 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 23, 2026, 6:52 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, Active Control, Multicenter Study to Evaluate the Efficacy at Week 52 of Secukinumab Monotherapy Compared With Adalimumab Monotherapy in Patients With Active Psoriatic Arthritis

Brief summary

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

This was a randomized, double-blind, active controlled, multicenter, parallel-group study evaluating secukinumab monotherapy and adalimumab monotherapy in approximately 850 patients with active psoriatic arthritis (PsA) who are naïve to biologic therapy and are intolerant or having inadequate response to conventional disease modifying anti-rheumatic drugs (also known as non-biologic DMARDs).

Study identification

NCT ID
NCT02745080
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
853 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
Apr 3, 2017 (Actual)
Primary completion
Dec 30, 2019 (Actual)
Completion
Dec 30, 2019 (Actual)
Last update posted
Jan 27, 2021

2017 – 2019

United States locations

U.S. sites
19
U.S. states
10
U.S. cities
19
Facility City State ZIP Site status
Novartis Investigative Site Fountain Valley California 92708 —
Novartis Investigative Site Fullerton California 92835 —
Novartis Investigative Site La Mesa California 91942 —
Novartis Investigative Site Upland California 91786 —
Novartis Investigative Site Bowling Green Kentucky 42101 —
Novartis Investigative Site St Louis Missouri 63117 —
Novartis Investigative Site Lincoln Nebraska 68516 —
Novartis Investigative Site Omaha Nebraska 68114 —
Novartis Investigative Site Rochester New York 14623 —
Novartis Investigative Site Bethlehem Pennsylvania 18015 —
Novartis Investigative Site Duncansville Pennsylvania 16635 —
Novartis Investigative Site Arlington Texas 76011 —
Novartis Investigative Site Austin Texas 78731 —
Novartis Investigative Site Dallas Texas 75231 —
Novartis Investigative Site Mesquite Texas 75150 —
Novartis Investigative Site Burlington Vermont 05401 —
Novartis Investigative Site Seattle Washington 98122 —
Novartis Investigative Site Spokane Washington 99204 —
Novartis Investigative Site Glendale Wisconsin 53217 —

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 137 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02745080, 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 Jan 27, 2021 · Synced Oct 23, 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 NCT02745080 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →