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Completed Phase 3 Interventional Results available

Study to Evaluate Maintenance of Sustained Remission of axSpA With CZP Compared to Placebo

ClinicalTrials.gov ID: NCT02505542

Public ClinicalTrials.gov record NCT02505542. 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 22, 2026, 6:02 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, Open-label (Part A) Followed by a Randomized, Double-blind, Parallel-group, Placebo Controlled Study (Part B) to Evaluate Maintenance of Remission in Subjects With Active Axial Spondyloarthritis (axSpA) Receiving Either Certolizumab Pegol 200 mg Q2W or 200 mg Q4W as Compared to Placebo

Brief summary

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

Patients receive study drug for one year (Part A). If, after the initial run-in phase, a sustained remission is reached they will be randomly split into one of three dose groups for another year (Part B). The maintenance of the sustained remission will be analyzed.

Study identification

NCT ID
NCT02505542
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB BIOSCIENCES GmbH
Industry
Enrollment
736 participants

Conditions and interventions

Interventions

Biological · Other

Eligibility (public fields only)

Age range
18 Years to 45 Years
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
Jul 2015 (Actual)
Primary completion
Feb 2019 (Actual)
Completion
Apr 2019 (Actual)
Last update posted
Dec 17, 2020

2015 – 2019

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
As0005 2313 Glendale Arizona 85304 —
As0005 2316 Mesa Arizona 85202 —
As0005 2314 Phoenix Arizona 85037 —
As0005 2317 Sun City Arizona 85351 —
As0005 2307 Palm Desert California 92260 —
As0005 2310 San Francisco California 94143 —
As0005 2305 Upland California 91786 —
As0005 2308 Denver Colorado 80230 —
As0005 2302 Brandon Florida 33511 —
As0005 2321 Hagerstown Maryland 21742 —
As0005 2312 Minot North Dakota 58701 —
As0005 2323 Oklahoma City Oklahoma 73101 —
As0005 2311 Duncansville Pennsylvania 16635 —
As0005 2315 Jackson Tennessee 38305 —
As0005 2303 Austin Texas 78731 —
As0005 2318 Dallas Texas 75231 —

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 92 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02505542, 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 Dec 17, 2020 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02505542 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →