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Completed

NCT Number: NCT00695188

Methotrexate Polyglutamate Levels as a Marker for the Clinical Outcome in the Treatment of Rheumatoid Arthritis

The primary objective is to determine whether erythrocyte polyglutamate levels are associated with objective clinical response in patients with rheumatoid arthritis after oral administration of low-dose methotrexate.The secondary aim of this study is to compare the efficacy and safety of standard dose methotrexate versus a higher starting dose.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Kaiser-Franz-Josef-Spital, Vienna, Austria

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About this study

The folate antagonist methotrexate (MTX) is currently one of the most widely used drugs for the treatment of rheumatoid arthritis (RA).Although MTX is very effective and well tolerated, the major drawback is the large interpatient variability in the clinical response.MTX is intracellularly converted by folylpolyglutamate synthetase (FPGS) to methotrexate polyglutamates (MTXPGs), which enhance the intracellular retention of MTX. Furthermore, the γ-linked sequential addition of glutamic acid residues inhibits finals steps in the de novo purine and pyrimidine biosynthesis, resulting in anti-proliferative and anti-inflammatory effects.76 adult, MTX-naive patients who fulfill the American College of Rheumatology criteria (ACR) for RA with a Disease Activity Score in 28 joints (DAS-28) > 3.2 are enrolled at two sites in Vienna (Austria).Clinical status is assessed by the number of joint counts and the Health Assessment Questionnaire (HAQ).Patients are randomly assigned to receive either a standard dose or a higher starting dose of 25 mg orally. In week 5, a subcutaneous dose of 25 mg is administered to each patient to get a reference level (bioavailability of 100%).The patients participate for 16 weeks, in which blood samples are collected at weeks 1, 2, 5, 6, 10 and 11 to perform pharmacokinetic analyses and metabolite measurements.The determination of erythrocyte MTXPG-levels is performed by using a HPLC technique.The primary outcome is the objective clinical response (measured in a rheumatic score, DAS-28), secondary outcome parameters are quality of life and routine laboratory parameters used in rheumatology. This clinical outcome will be correlated with MTX pharmacokinetics in blood, MTXPG kinetics in erythrocytes, and their impact on the folate pathway.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • MTX-naive
  • Age > 18 years
  • DAS-28 > 3.2
  • American College of Rheumatology-criteria for RA
  • Chest-X-ray
  • Informed consent
  • Prednisolon < 10 mg a day

Exclusion criteria

  • Pregnancy
  • Lactation
  • Renal and hepatic impairment
  • Malignant diseases (last 5 years)
  • Contraindications
  • Human Immunodeficiency Virus (HIV), Hepatitis B and C

Treatment and study plan

methotrexate

Drug

oral administration Escalating dose (15, 20, 25 mg)

Primary outcomes

  1. DAS-28 (Disease Activity Score in 28 Joints)

    Time frame: 16 weeks

    DAS stands for "Disease Activity Score" and is a measure of the activity of rheumatoid arthritis. In Europe the DAS is the recognized standard in research and clinical practice.

    The following parameters are included in the calculation:

    • Number of joints tender to the touch (TEN)
    • Number of swollen joints (SW)
    • Erythrocyte sedimentation rate (ESR)
    • Patient assessment of disease activity (VAS; mm)

    The DAS-28 is evaluated using a scale:

    0 - 3.2: low disease activity 3.2 - 5.1: moderate disease activity > 5.1: severe disease activity

Secondary outcomes

  1. HAQ (Health Assessment Questionnaire)

    Time frame: 16 weeks

Sponsors and collaborators

Lead sponsor

Ludwig-Boltzmann Institut fuer Rheumatologie, Balneologie und Rehabilitation

Other

Registry information

Official study title

Methotrexate Polyglutamate Levels as a Marker for the Clinical Outcome in the Treatment of Rheumatoid Arthritis A Multicenter, Randomized, Double-blind, Controlled Phase IV Trial

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Jun 11, 2008
Registry last updated
Feb 17, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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