Comparative Study of the Clinical Response and Cardiorespiratory Endurance in Early Rheumatoid Arthritis Patients Treated With Tocilizumab or Methotrexate (TOMERA)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified May 2010 by Université Catholique de Louvain.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Université Catholique de Louvain
ClinicalTrials.gov Identifier:
NCT01245452
First received: November 19, 2010
Last updated: NA
Last verified: May 2010
History: No changes posted
  Purpose

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.


Condition Intervention
Rheumatoid Arthritis
Drug: Tocilizumab
Drug: Methotrexate

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
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 From Early Rheumatoid Arthritis Patients Treated With Tocilizumab or Methotrexate

Resource links provided by NLM:


Further study details as provided by Université Catholique de Louvain:

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. [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    not necessary


Secondary Outcome Measures:
  • To analyze the clinical efficacy of Tocilizumab in this population. [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    no necessary

  • To correlate the CRE response with other marker (CRP, Hb, DAS, HAQ). [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    no necessary

  • To evaluate the safety profile of Tocilizumab. [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
    no necessary


Estimated Enrollment: 30
Study Start Date: May 2010
Estimated Study Completion Date: May 2012
Estimated Primary Completion Date: May 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Tocilizumab
Tocilizumab (8 mg/kg monthly from week 0 to 20)
Drug: Tocilizumab
Tocilizumab (8 mg/kg monthly from week 0 to 20)
Other Names:
  • Roche EU/1/08/492/001
  • ATC code L04AC07
Active Comparator: Methotrexate
MTX at a dose ranging from 10 mg/week at baseline to 20 mg/week at week 8
Drug: Methotrexate
MTX at a dose ranging from 10 mg/week at baseline to 20 mg/week at week 8

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.

  Eligibility

Ages Eligible for Study:   18 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

Diagnosis of RA (according to ACR criteria) Disease duration < 2 years. Age between 18 and 70 years old. Active RA defined by a DAS28-CRP score > 3.2 with a swollen joint count ≥ 4 MTX naive Stable therapy with corticosteroids or 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.

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01245452

Contacts
Contact: Patrick DUREZ, MD +3227645389 patrick.durez@uclouvain.be
Contact: Geneviève DEPRESSEUX +3227645395 genevieve.depresseux@uclouvain.be

Locations
Belgium
Université Catholique de Louvain Recruiting
Bruxelles, Belgium, 1200
Contact: Patrick DUREZ, Md     +3227645389     patrick.durez@uclouvain.be    
Contact: Geneviève DEPRESSEUX     +3227645395     genevieve.depresseux@uclouvain.be    
Principal Investigator: Patrick DUREZ, Md            
Sponsors and Collaborators
Université Catholique de Louvain
Investigators
Principal Investigator: Patrick DUREZ, Md Université Catholique de Louvain
  More Information

No publications provided

Responsible Party: Université Catholique de Louvain, Not available
ClinicalTrials.gov Identifier: NCT01245452     History of Changes
Other Study ID Numbers: P1200/002
Study First Received: November 19, 2010
Last Updated: November 19, 2010
Health Authority: Belgium: Federal Agency for Medicines and Health Products, FAMHP

Keywords provided by Université Catholique de Louvain:
Rheumatoid arthritis
Tocilizumab
Cardiorespiratory endurance

Additional relevant MeSH terms:
Arthritis
Arthritis, Rheumatoid
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases
Connective Tissue Diseases
Autoimmune Diseases
Immune System Diseases
Methotrexate
Abortifacient Agents, Nonsteroidal
Abortifacient Agents
Reproductive Control Agents
Physiological Effects of Drugs
Pharmacologic Actions
Therapeutic Uses
Antimetabolites, Antineoplastic
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents
Dermatologic Agents
Enzyme Inhibitors
Folic Acid Antagonists
Immunosuppressive Agents
Immunologic Factors
Antirheumatic Agents
Nucleic Acid Synthesis Inhibitors

ClinicalTrials.gov processed this record on June 17, 2013