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Terminated Phase 4 Interventional Results available

A Study of RoActemra/Actemra (Tocilizumab) Versus Adalimumab in Combination With Methotrexate (MTX) in Patients With Moderate to Severe Active Rheumatoid Arthritis And an Inadequate Response to Treatment With Only One Tumor Necrosis Factor (TNF)-Inhibitor

ClinicalTrials.gov ID: NCT01283971

Public ClinicalTrials.gov record NCT01283971. 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 24, 2026, 9:57 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, Open-label, Parallel-group Study of the Reduction of Signs and Symptoms During Treatment With Tocilizumab Versus Adalimumab, Both in Combination With MTX, in Patients With Moderate to Severe Active Rheumatoid Arthritis and an Inadequate Response to Treatment With Only One TNF Inhibitor

Brief summary

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

This randomized, parallel-group study will assess the efficacy and safety of RoActemra/Actemra (tocilizumab) versus adalimumab, both in combination with methotrexate (MTX) in patients with moderate to severe active rheumatoid arthritis. Patients, already treated with MTX at stable doses, will be randomized to receive either RoActemra/Actemra 8 mg/kg intravenously (IV) every 4 weeks or adalimumab 40 mg subcutaneous (SC) every 2 weeks. All patients will receive methotrexate (10-25 mg weekly) and folate (at least 5 mg weekly). The anticipated time on study treatment is 24 weeks.

Study identification

NCT ID
NCT01283971
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
96 participants

Conditions and interventions

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 30, 2011
Primary completion
Jul 31, 2012
Completion
Jul 31, 2012
Last update posted
Feb 9, 2014

2011 – 2012

United States locations

U.S. sites
107
U.S. states
32
U.S. cities
98
Facility City State ZIP Site status
Not listed Huntsville Alabama 35801 —
Not listed Phoenix Arizona 85027 —
Not listed Tucson Arizona 85712 —
Not listed Covina California 91723 —
Not listed Escondido California 92025 —
Not listed Huntington Beach California 92646 —
Not listed La Mesa California 91942 —
Not listed Lakewood California 90712 —
Not listed Long Beach California 90806 —
Not listed Los Angeles California 90048 —
Not listed Sacramento California 95816-5119 —
Not listed San Diego California 92108 —
Not listed Westlake Village California 91361 —
Not listed Whittier California 90603 —
Not listed Whittier California 90606 —
Not listed Bridgeport Connecticut 06606 —
Not listed Hamden Connecticut 06518 —
Not listed Norwich Connecticut 06360 —
Not listed Newark Delaware 19713 —
Not listed Aventura Florida 33180 —
Not listed Fort Lauderdale Florida 33334 —
Not listed Jupiter Florida 33458 —
Not listed Melbourne Florida 32901 —
Not listed Naples Florida 34102 —
Not listed Ocala Florida 34474 —
Not listed Orlando Florida 32806 —
Not listed Ormond Beach Florida 32174 —
Not listed Palm Habor Florida 34684 —
Not listed Palm Harbor Florida 34684 —
Not listed Sarasota Florida 34239 —
Not listed Tamarac Florida 33321 —
Not listed Tampa Florida 33609 —
Not listed Atlanta Georgia 30342 —
Not listed Valdosta Georgia 31602 —
Not listed Idaho Falls Idaho 83404 —
Not listed Chicago Illinois 60611 —
Not listed Maywood Illinois 60153 —
Not listed Moline Illinois 61265 —
Not listed Springfield Illinois 62704 —
Not listed Fort Wayne Indiana 46804 —
Not listed South Bend Indiana 46601 —
Not listed Lexington Kentucky 40515 —
Not listed Baton Rouge Louisiana 70808 —
Not listed Monroe Louisiana 71203 —
Not listed Annapolis Maryland 21401 —
Not listed Cumberland Maryland 21502 —
Not listed Frederick Maryland 21702 —
Not listed Hagerstown Maryland 21740 —
Not listed Fall River Massachusetts 02720 —
Not listed Worcester Massachusetts 01610 —
Not listed Battle Creek Michigan 49015 —
Not listed Lansing Michigan 48910 —
Not listed Petoskey Michigan 49770 —
Not listed Saint Claire Shores Michigan 48081 —
Not listed Biloxi Mississippi 39531 —
Not listed Flowood Mississippi 39232 —
Not listed Tupelo Mississippi 38802 —
Not listed Springfield Missouri 65807 —
Not listed St Louis Missouri 63117 —
Not listed Reno Nevada 89502 —
Not listed Clifton New Jersey 07012 —
Not listed Manalapan New Jersey 07726 —
Not listed New Brunswick New Jersey 08903 —
Not listed Brooklyn New York 11201 —
Not listed New York New York 10016 —
Not listed New York New York 10029-6574 —
Not listed Syracuse New York 13210 —
Not listed Charlotte North Carolina 28204 —
Not listed Charlotte North Carolina 28210 —
Not listed Greensboro North Carolina 27408 —
Not listed Greenville North Carolina 27834 —
Not listed Raleigh North Carolina 27617 —
Not listed Washington North Carolina 27889 —
Not listed Cleveland Ohio 44195 —
Not listed Middleburg Heights Ohio 44130 —
Not listed Toledo Ohio 43606 —
Not listed Oklahoma City Oklahoma 73109 —
Not listed Lake Oswego Oregon 97035 —
Not listed Duncansville Pennsylvania 16635 —
Not listed Philadelphia Pennsylvania 19152 —
Not listed Pittsburgh Pennsylvania 15237 —
Not listed Pittsburgh Pennsylvania 15261 —
Not listed Willow Grove Pennsylvania 19090 —
Not listed Wynnewood Pennsylvania 19096 —
Not listed Wyomissing Pennsylvania 19610 —
Not listed Charleston South Carolina 29406 —
Not listed Myrtle Beach South Carolina 29572 —
Not listed Jackson Tennessee 38305 —
Not listed Memphis Tennessee 38104 —
Not listed Memphis Tennessee 38119 —
Not listed Austin Texas 78731 —
Not listed Carrollton Texas 75007 —
Not listed Corpus Christi Texas 78404 —
Not listed Houston Texas 77004 —
Not listed Houston Texas 77034 —
Not listed Houston Texas 77070 —
Not listed Houston Texas 77074 —
Not listed Mesquite Texas 75150 —
Not listed San Antonio Texas 78217 —
Not listed San Antonio Texas 78258 —
Not listed Sugar Land Texas 77479 —
Not listed Arlington Virginia 22205 —
Not listed Kennewick Washington 99336 —
Not listed Spokane Washington 99204 —
Not listed Tacoma Washington 98405 —
Not listed Clarksburg West Virginia 26301 —
Not listed 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 63 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01283971, 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 Feb 9, 2014 · Synced Sep 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01283971 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →