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Completed Phase 3 Interventional Results available

Certolizumab Pegol in Subjects With Active Axial Spondyloarthritis

ClinicalTrials.gov ID: NCT01087762

Public ClinicalTrials.gov record NCT01087762. 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, 8:11 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

Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Efficacy and Safety of Certolizumab Pegol in Subjects With Active Axial Spondyloarthritis

Brief summary

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

The study is a Phase 3, multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of two dose regimens of Certolizumab Pegol (CZP) in subjects with active axial Spondyloarthritis (axial SpA).

Study identification

NCT ID
NCT01087762
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB BIOSCIENCES GmbH
Industry
Enrollment
325 participants

Conditions and interventions

Interventions

Biological · Other

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
Mar 2010 (Type not available)
Primary completion
Oct 2011 (Actual)
Completion
Aug 2015 (Actual)
Last update posted
Aug 1, 2018

2010 – 2015

United States locations

U.S. sites
32
U.S. states
17
U.S. cities
31
Facility City State ZIP Site status
961 Birmingham Alabama — —
953 Tuscaloosa Alabama — —
954 Peoria Arizona — —
971 Scottsdale Arizona — —
987 Tucson Arizona — —
974 La Jolla California — —
973 Los Angeles California — —
966 Palm Desert California — —
952 San Diego California — —
957 Aventura Florida — —
962 Fort Lauderdale Florida — —
959 Orange Park Florida — —
990 Pinellas Park Florida — —
958 Vero Beach Florida — —
964 Hagerstown Maryland — —
969 Eagan Minnesota — —
984 Flowood Mississippi — —
965 Florissant Missouri — —
950 St Louis Missouri — —
985 Brooklyn New York — —
963 Asheville North Carolina — —
977 Cleveland Ohio — —
951 Middleburg Heights Ohio — —
970 Oklahoma City Oklahoma — —
982 Portland Oregon — —
972 Duncansville Pennsylvania — —
975 Dallas Texas — —
978 Houston Texas — —
983 Houston Texas — —
967 San Antonio Texas — —
981 Salt Lake City Utah — —
968 Seattle Washington — —

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 72 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01087762, 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 1, 2018 · Synced Oct 26, 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 NCT01087762 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →