search
Back to results

Study of the Response and Cardiorespiratory Endurance in Early RA Patients Treated With Tocilizumab or Methotrexate (TOMERA)

Primary Purpose

Rheumatoid Arthritis

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Tocilizumab
Methotrexate
Sponsored by
Patrick Durez
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rheumatoid Arthritis focused on measuring Rheumatoid arthritis, Tocilizumab, Cardiorespiratory endurance

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of RA (according to American College of Rheumatology ACR criteria)
  • Disease duration < 2 years.
  • Age between 18 and 70 years old.
  • Active RA defined by a disease activity score 28 DAS28-CRP score > 3.2 with a swollen joint count ≥ 4
  • MTX naive
  • Stable therapy with corticosteroids or nonsteroidal anti-inflammatory drug NSAIDs
  • Presence of knee arthralgia or synovitis (addendum protocol with synovial biopsy).

Exclusion Criteria:

Previous MTX treatment. Exclusion for severe physical handicap to perform CRE. Exclusion for general safety (history of severe allergic reaction, sepsis, malignancy within 5 years, pregnancy, severe heart failure) Concurrent treatment with other DMARDs than MTX or any anti-TNF and biological therapies.

Sites / Locations

  • Université Catholique de Louvain

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Tocilizumab

Methotrexate

Arm Description

Tocilizumab (8 mg/kg monthly from week 0 to 20)

MTX at a dose ranging from 10 mg/week at baseline to 20 mg/week at week 8

Outcomes

Primary Outcome Measures

To measure the CRE by a work capacity index obtained in a submaximal testing (W65%/kg) in early RA patients treated with tocilizumab compared to Methotrexate alone.
not necessary

Secondary Outcome Measures

To analyze the clinical efficacy of Tocilizumab in this population.
no necessary
To correlate the CRE response with other marker (CRP, Hb, Disease activity score DAS, HAQ).
no necessary
To evaluate the safety profile of Tocilizumab.
no necessary
To assess the effect of Tocilizumab on synovial histopathology of early RA
not necessary

Full Information

First Posted
November 19, 2010
Last Updated
October 30, 2013
Sponsor
Patrick Durez
search

1. Study Identification

Unique Protocol Identification Number
NCT01245452
Brief Title
Study of the Response and Cardiorespiratory Endurance in Early RA Patients Treated With Tocilizumab or Methotrexate
Acronym
TOMERA
Official Title
Comparative Study of the Clinical Response and Cardiorespiratory Endurance in Early Rheumatoid Arthritis Patients Treated With Tocilizumab or Methotrexate Addendum Protocol : Global Gene Expression Profiles in Synovial Biopsies
Study Type
Interventional

2. Study Status

Record Verification Date
October 2013
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Patrick Durez

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
To measure the CRE by a work capacity index obtained in a submaximal testing (W65%/kg) in early RA patients treated with tocilizumab compared to Methotrexate alone. The secondary endpoints : analyze the clinical efficacy of Tocilizumab in this population and correlate the CRE response with other marker (CRP, Hb, DAS, HAQ) and evaluate the safety profile of Tocilizumab.
Detailed Description
Rheumatoid arthritis (RA) is the most prevalent (about 1%) inflammatory rheumatic disorder. Interleukin-6 (IL-6) has emerged as a potential therapeutic target in RA. This is based on the greater understanding of the role this cytokine can play in various aspects of the pathogenesis of RA. It has been shown that IL-6 is responsible for various clinical symptoms, including,fatigue, anemia, anorexia, fever, as well as the production of autoantibodies and increase in the erythrocyte sedimentation rate, all of which develop in patients with RA. Tocilizumab, as monotherapy and in combination with methotrexate, has been shown to be effective for RA patients with insufficient response to methotrexate or other disease-modifying antirheumatic drugs. These observations about the effects of tocilizumab were extended to patients refractory to tumor necrosis factor inhibitors. Tocilizumab also slows down the progression of structural joint damage. Furthermore, a 5-year long-term safety and efficacy has been shown. The place of Tocilizumab therapy in early RA is still unknown. Cardiorespiratory endurance (CRE), the most fundamental component of physical fitness can be severely impaired in patients with rheumatoid arthritis (RA). It has been shown that intensive and early treatment of RA can induce sustained clinical remission, improve general health and physical fitness and might therefore have an impact on the quality of life of RA patient. This study was planned to measure the CRE by a work capacity index obtained in a submaximal testing (W65%/kg) in early RA patients treated with tocilizumab compared to Methotrexate alone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rheumatoid Arthritis
Keywords
Rheumatoid arthritis, Tocilizumab, Cardiorespiratory endurance

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tocilizumab
Arm Type
Experimental
Arm Description
Tocilizumab (8 mg/kg monthly from week 0 to 20)
Arm Title
Methotrexate
Arm Type
Active Comparator
Arm Description
MTX at a dose ranging from 10 mg/week at baseline to 20 mg/week at week 8
Intervention Type
Drug
Intervention Name(s)
Tocilizumab
Other Intervention Name(s)
Roche EU/1/08/492/001, ATC code L04AC07
Intervention Description
Tocilizumab (8 mg/kg monthly from week 0 to 20)
Intervention Type
Drug
Intervention Name(s)
Methotrexate
Intervention Description
MTX at a dose ranging from 10 mg/week at baseline to 20 mg/week at week 8
Primary Outcome Measure Information:
Title
To measure the CRE by a work capacity index obtained in a submaximal testing (W65%/kg) in early RA patients treated with tocilizumab compared to Methotrexate alone.
Description
not necessary
Time Frame
2 years
Secondary Outcome Measure Information:
Title
To analyze the clinical efficacy of Tocilizumab in this population.
Description
no necessary
Time Frame
2 years
Title
To correlate the CRE response with other marker (CRP, Hb, Disease activity score DAS, HAQ).
Description
no necessary
Time Frame
2 years
Title
To evaluate the safety profile of Tocilizumab.
Description
no necessary
Time Frame
2 years
Title
To assess the effect of Tocilizumab on synovial histopathology of early RA
Description
not necessary
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of RA (according to American College of Rheumatology ACR criteria) Disease duration < 2 years. Age between 18 and 70 years old. Active RA defined by a disease activity score 28 DAS28-CRP score > 3.2 with a swollen joint count ≥ 4 MTX naive Stable therapy with corticosteroids or nonsteroidal anti-inflammatory drug NSAIDs Presence of knee arthralgia or synovitis (addendum protocol with synovial biopsy). Exclusion Criteria: Previous MTX treatment. Exclusion for severe physical handicap to perform CRE. Exclusion for general safety (history of severe allergic reaction, sepsis, malignancy within 5 years, pregnancy, severe heart failure) Concurrent treatment with other DMARDs than MTX or any anti-TNF and biological therapies.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patrick DUREZ, Md
Organizational Affiliation
Université Catholique de Louvain
Official's Role
Principal Investigator
Facility Information:
Facility Name
Université Catholique de Louvain
City
Bruxelles
ZIP/Postal Code
1200
Country
Belgium

12. IPD Sharing Statement

Learn more about this trial

Study of the Response and Cardiorespiratory Endurance in Early RA Patients Treated With Tocilizumab or Methotrexate

We'll reach out to this number within 24 hrs