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Completed Phase 4 Interventional Results available

Study to Assess the Short- and Long-term Efficacy of Certolizumab Pegol Plus Methotrexate Compared to Adalimumab Plus Methotrexate in Subjects With Moderate to Severe Rheumatoid Arthritis (RA) Inadequately Responding to Methotrexate

ClinicalTrials.gov ID: NCT01500278

Public ClinicalTrials.gov record NCT01500278. 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 Sep 4, 2026, 11:04 AM 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, Single-blind, Randomized Parallel-group Study to Assess the Short- and Long-term Efficacy of Certolizumab Pegol Plus Methotrexate Compared to Adalimumab Plus Methotrexate in Subjects With Moderate to Severe Rheumatoid Arthritis Responding Inadequately to Methotrexate

Brief summary

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

This study is conducted to evaluate the short (12 Weeks) and long term (104 Weeks) efficacy of Certolizumab Pegol compared with Adalimumab both in combination with Methotrexate (MTX) in the treatment of moderate to severe Rheumatoid Arthritis (RA) that is not responding adequately to MTX.

Study identification

NCT ID
NCT01500278
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
UCB Pharma SA
Industry
Enrollment
915 participants

Conditions and interventions

Interventions

Biological · Drug

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, 2011
Primary completion
Oct 31, 2015
Completion
Dec 31, 2015
Last update posted
Jul 30, 2018

2011 – 2016

United States locations

U.S. sites
62
U.S. states
27
U.S. cities
59
Facility City State ZIP Site status
141 Birmingham Alabama
214 Tuscaloosa Alabama
159 Tucson Arizona
152 Hot Springs Arkansas
147 Covina California
161 Fullerton California
217 La Mesa California
149 Los Angeles California
144 Menifee California
185 Roseville California
208 Sacramento California
189 Van Nuys California
148 Whittier California
220 Lewes Delaware
142 Aventura Florida
216 Fort Lauderdale Florida
162 Gainesville Florida
209 Vero Beach Florida
145 Coeur d'Alene Idaho
202 Maywood Illinois
134 Lexington Kentucky
178 Baltimore Maryland
137 Battle Creek Michigan
153 Detroit Michigan
155 Lansing Michigan
204 Eagan Minnesota
180 Rochester Minnesota
143 Saint Louis Park Minnesota
135 Omaha Nebraska
170 Reno Nevada
201 Teaneck New Jersey
150 Voorhees Township New Jersey
205 Albuquerque New Mexico
154 Albany New York
136 Brooklyn New York
219 Orchard Park New York
207 Plainview New York
167 Syracuse New York
140 Cincinnati Ohio
184 Oklahoma City Oklahoma
164 Bethlehem Pennsylvania
132 Duncansville Pennsylvania
190 Wyomissing Pennsylvania
210 Charleston South Carolina
187 Myrtle Beach South Carolina
203 Orangeburg South Carolina
133 Jackson Tennessee
160 Knoxville Tennessee
138 Austin Texas
151 Corpus Christi Texas
131 Dallas Texas
146 Dallas Texas
213 Dallas Texas
166 Houston Texas
212 Houston Texas
139 San Antonio Texas
181 Sugar Land Texas
165 Victoria Texas
211 Arlington Virginia
157 Spokane Washington
163 Clarksburg West Virginia
215 Glendale Wisconsin

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 113 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01500278, 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 Jul 30, 2018 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01500278 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →