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Completed Phase 3 Interventional Results available

A Study of Tocilizumab and Methotrexate Treatment Strategies (Adding Tocilizumab to Methotrexate Versus Switching to Tocilizumab) in Patients With Active Rheumatoid Arthritis With Inadequate Response to Prior Methotrexate Treatment

ClinicalTrials.gov ID: NCT00810199

Public ClinicalTrials.gov record NCT00810199. 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 Jul 22, 2026, 7:34 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

Randomized Placebo-controlled Study of Two Treatment Strategies Based on Tocilizumab (TCZ) With or Without Methotrexate (MTX) and Possible Addition of Other Disease-modifying Anti-rheumatic Drugs (DMARDs) in Patients...

Study identification

NCT ID
NCT00810199
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
556 participants

Conditions and interventions

Interventions

  • tocilizumab [RoActemra/Actemra] Drug
  • methotrexate Drug
  • placebo Drug

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
Feb 28, 2009
Primary completion
Jul 31, 2010
Completion
Dec 31, 2012
Last update posted
Jul 17, 2014

2009 – 2013

United States locations

U.S. sites
21
U.S. states
11
U.S. cities
21
Facility City State ZIP Site status
Not listed Santa Monica California 90404
Not listed Upland California 91786
Not listed Whittier California 90606
Not listed Aventura Florida 33180
Not listed Naples Florida 34102
Not listed Orange Park Florida 32073
Not listed Plantation Florida 33317
Not listed Sarasota Florida 34239
Not listed South Miami Florida 33143
Not listed Tamarac Florida 33321
Not listed Eagan Minnesota 55121
Not listed Las Vegas Nevada 89128
Not listed Mayfield Ohio 44143
Not listed Middleburg Heights Ohio 44130
Not listed Oklahoma City Oklahoma 73104
Not listed West Reading Pennsylvania 19611
Not listed Greenville South Carolina 29601
Not listed Nashville Tennessee 37205
Not listed Houston Texas 77004
Not listed San Antonio Texas 78217
Not listed Spokane Washington 99204

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 116 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00810199, 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 17, 2014 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00810199 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →