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Effect of Monoclonal Anti-IL6 Antibody (Tocilizumab) on the Cardiovascular Risk in Patients With Rheumatoid Arthritis (TOCRIVAR)

7 februari 2017 uppdaterad av: Hospital Universitario de Canarias

The purpose of this study is to determine whether tocilizumab changes the cardiovascular risk factors on patients with arthritis rheumatoid.

Study hypothesis: the IL-6 contributes to increase the cardiovascular risk factors of patients with rheumatoid arthritis because it produces systemic effects as increasing weight and atherogenic body fat, changing energy homeostasis and inducing the adipokines production and the insulin resistence.

Studieöversikt

Status

Okänd

Betingelser

Intervention / Behandling

Studietyp

Interventionell

Inskrivning (Förväntat)

28

Fas

  • Fas 4

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Santa Cruz de Tenerife
      • La Laguna, Santa Cruz de Tenerife, Spanien, 38320
        • Hospital Universitario de Canarias

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 70 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  1. Age ≥ 18 and <70 years.
  2. Diagnosis of active Rheumatoid Arthritis, moderate to severe (≥ 3.2 DAS28) of ≥ 6 months duration.
  3. Patients with an inadequate clinical response to a stable dose of non-biological DMARDs or anti-TNF treatment for a period ≥ 8 weeks before treatment.
  4. If patients are receiving oral corticosteroids, the dose should have been ≤ 10 mg predinosona and stable for at least one month before the start of treatment (day 1).
  5. Patients who are able and wish to sign the informed consent and comply with the requirements of the study protocol.

Exclusion Criteria:

  1. Major surgery (including joints surgery) within eight weeks prior to the screening visit or major surgery scheduled for six months after first infusion.
  2. Other Rheumatic autoimmune diseases, including systemic lupus erythematosus (SLE), mixed connective tissue disease (MCTD), scleroderma, polymyositis or systemic involvement secondary to AR (such as vasculitis, pulmonary fibrosis or Felty's syndrome). It's allowed the inclusion of patients with interstitial pulmonary fibrosis and be still able to tolerate treatment with MTX. Sjögren's syndrome with RA is not considered exclusion criterion.
  3. Rheumatoid arthritis with Functional Class IV as defined in the RA Classification of the ACR (complete or significant disability of patients, confined to bed or to the wheelchair and without possibilities to take care themselves).
  4. Prior or actual inflammatory joint disease different of RA (eg, gout, reactive arthritis, psoriatic arthritis, seronegative spondyloarthropathy, Lyme disease).

    Specific drug criteria

  5. Treatment with any investigational agent in the four weeks before the screening visit (or time equivalent to five half-lives of the investigational drug, whichever is longer).
  6. Immunization with a live vaccine / attenuated in the four weeks prior to the baseline visit.
  7. Pretreatment with TCZ Laboratory Tests (at the screening visit)
  8. Serum creatinine> 142 mmol / l (1.6 mg / dL) in women and> 168 mmol / l (1.9 mg / dl) in men and absence of active renal disease.
  9. ALT (SGPT) and AST (SGOT)> 1.5 ULN (if the initial sample of ALT [SGPT] or AST [SGOT] gives a value> 1.5 times ULN, you can take and analyze a second sample during the selection period).
  10. Platelet count <100 x 109 / l (100.000/mm3).
  11. Hemoglobin <85 g / dl (<8.5 g / l, 5.3 mmol / l).
  12. Leukocytes <1.0 x 109 / l (1000/mm3), ANC <0.5 x 109 / L (500/mm3).
  13. RAL <0.5 x 109 / L (500/mm3).
  14. Positivity for surface antigen of hepatitis B (HBsAg) and antibodies to hepatitis C.
  15. Total bilirubin> ULN (if the initial sample of bilirubin> ULN, you can take and analyze a second sample during the selection period).
  16. Triglycerides> 10 mmol / l (> 900 mg / dl) at the screening visit (non fasting).
  17. Pregnant or lactating women.
  18. not use of reliable means of contraception, such as a physical barrier (patient and partner), pill or contraceptive patch, spermicide and barrier or IUD.
  19. Background of serious allergic or anaphylactic reactions to human monoclonal antibodies, humanized or murine.
  20. RXT evidence of clinically significant abnormality.
  21. Evidence of uncontrolled concomitant serious illness, cardiovascular, nervous system, lung (including obstructive pulmonary disease), renal, hepatic, endocrine (including uncontrolled diabetes mellitus), or gastrointestinal.
  22. history of diverticulitis, diverticulosis in antibiotic treatment, the physician should consider the benefit-risk ratio.
  23. Background of lower GI ulcer disease as the Crohn's disease, ulcerative colitis or other symptomatic conditions predisposed to perforations lower GI
  24. Uncontrolled diseases such as asthma, psoriasis or inflammatory bowel disease,... treated normally with corticosteroids orally or parenterally.
  25. Ongoing liver disease as determined by the principal investigator. (Patients with a history of elevated ALT (SGPT) will not be excluded)
  26. Active infections or recurrent infections in the past by mycobacteria, fungus, virus or bacteria (for example: tuberculosis, atypical mycobacterial disease, clinically significant abnormalities in RXT, hepatitis B and C, herpes zoster), or any major episode infection that required hospitalization or IV antibiotic treatment in the 4 weeks preceding the screening visit or oral antibiotic in the 2 weeks prior to the screening visit.
  27. Primary or secondary immunodeficiency.
  28. Evidence of active malignancy diagnosed within 5 years before the inclusion(including solid tumors and hematological), or breast cancer diagnosed in the previous 5 years.
  29. Active tuberculosis (TB) requiring treatment within 3 years above. Patients with a positive skin test tuberculin purified protein derivative (PPD) at the screening visit. Patients treated for tuberculosis no recurrence in the last three years will not be excluded.
  30. HIV positive patients.
  31. History of alcoholism, drug addiction or drug abuse in the six months before the screening visit.
  32. Painful neuropathies or other conditions that may interfere with the pain assessment.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Stödjande vård
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Övrig: tocilizumab

All the patients are treated with tocilizumab before inclusion. The doses, frequency and duration are in acordance with the Summary of Characteristics of the Product authorised by EMA.

Usually 8mg/kg (not minor than 480 mg), once each 4 weeks.

At the moment of the ecography, the clinician evaluates the endothelial responses via applying braquial ischemia and administering sublingual nitroglicerin spray to evaluate vasodilation.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Framingham Point Scores
Tidsram: Baseline and 52 weeks
Proportion of changes in Framingham Point Scores
Baseline and 52 weeks

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Liver enzymes
Tidsram: Baseline, 12, 24 and 52 weeks
Number of patients with liver enzymes elevated.
Baseline, 12, 24 and 52 weeks
Lipoprotein levels
Tidsram: Baseline, 12, 24 and 52 weeks
Number of patients with elevated lipoprotein levels
Baseline, 12, 24 and 52 weeks
DAS28 score
Tidsram: Baseline and 52 week
Variation in DAS28 score after tocilizumab
Baseline and 52 week
Number of patients with Adverse Drug Reactions
Tidsram: up to 52 weeks
Number of patients with Adverse Drug Reactions as a measure of safety
up to 52 weeks
Insulinemia
Tidsram: Baseline and 52 week
Change in insulinemia 52 weeks later.
Baseline and 52 week

Andra resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Proportion of brachial artery vasodilation
Tidsram: Baseline, 24 and 52 weeks
To evaluate the endothelial responses to ischemia and vasodilatation by ecography
Baseline, 24 and 52 weeks
cytokines, adipokines and adhesion molecules levels
Tidsram: Baseline and 52 week
To evaluate changes in cytokines, adipokines and adhesion molecules
Baseline and 52 week

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Samarbetspartners

Utredare

  • Huvudutredare: Federico Díaz González, MD, PhD, Hospital Universitario de Canarias

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 december 2011

Primärt slutförande (Förväntat)

1 mars 2017

Avslutad studie (Förväntat)

1 mars 2017

Studieregistreringsdatum

Först inskickad

3 december 2012

Först inskickad som uppfyllde QC-kriterierna

18 december 2012

Första postat (Uppskatta)

19 december 2012

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

9 februari 2017

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

7 februari 2017

Senast verifierad

1 februari 2017

Mer information

Termer relaterade till denna studie

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