MethMax Trial: MAXimising the METHotrexate Therapy Potential in Patients with Active Rheumatoid Arthritis

Official title

An International, Multicentre, Interventional, Randomised, Assessor-blinded Trial to MAXimise the METHotrexate Therapy Potential in Patients with Active Rheumatoid Arthritis

Overview

The MethMax trial is a prospective, international, multicentre, randomised, assessor-blinded, parallel-group, low intervention study. Patients with active rheumatoid arthritis treated with oral methotrexate up to 25mg weekly will be randomised in 50:50 fashion to receive 25mg oral vs subcutaneous methotrexate for the period of 24 weeks. In regular visits, patient reported outcomes, clinical disease activity, therapy adherence and diverse established and exploratory biomarkers will be assessed.

Detailed description

Methotrexate is recommended as the first-line therapy in patients with rheumatoid arthritis. However, a significant proportion of patients does not achieve disease remission with methotrexate monotherapy, which can be attributed to multiple reasons. We hypothesize, that the efficacy limitations of this well-known medication can be, to some extent, overcome by sufficient dose and route optimisation. Furthermore, individual factors effecting the treatment response are unknown. Thus, we aim to evaluate the "maximised methotrexate therapy" before switching to biologic or targeted synthetic drugs.

The MethMax trial is a prospective, randomised, assessor-blinded, parallel-group, low-intervention trial, including 182 patients across 7 European countries. Patients with active rheumatoid arthritis, naïve to biologic or targeted synthetic antirheumatic drugs, who have been on a stable oral methotrexate therapy for the past 3 months will be randomised in 1:1 ratio to either 25mg oral or 25mg subcutaneous methotrexate weekly. In both arms, a short glucocorticoid therapy will be prescribed at baseline visit. The active study duration for each patient is 24 weeks. After inclusion, study visits take place at baseline, weeks 4, 8, 12, 16 and 24. The clinical efficacy and safety parameters will be obtained at each visit. At predefined timepoints, further patient reported outcomes, exploratory biomarkers like sweat and blood metabolites, as well as medication adherence will be assessed. Written consent will be obtained for all participants. The study has received regulatory approval via the Clinical Trials Information System and has recently started recruitment at the first centre.

The anticipated results will suggest whether the subcutaneous administration of 25mg methotrexate weekly is superior to oral methotrexate 25mg and lower doses in each route respectively. The outcomes include clinical disease activity, methotrexate metabolism analyses and medication adherence. The gained knowledge could lead to individual therapy optimisation and new therapy recommendations.

Interventions

• Drug Methotrexate
  comparison between oral and subcutaneous methotrexate dosis of 25mg

Primary outcome measures

• CDAI remission (≤2.8) at week 24 [Time frame: 24 weeks]

Secondary outcome measures (12)

• CDAI low disease activity (≤10) at week 24 [Time frame: 24 weeks]
• CDAI remission (≤2.8) at week 12 [Time frame: 12 weeks]
• CDAI low disease activity (≤10) at week 12 [Time frame: 12 weeks]
• ACR20% response at week 24 [Time frame: 24 weeks]
• ACR20% response at week 12 [Time frame: 12 weeks]
• ACR50% response at week 24 [Time frame: 24 weeks]
• ACR50% response at week 12 [Time frame: 12 weeks]
• ACR70% response at week 24 [Time frame: 24 weeks]
• ACR70% response at week 12 [Time frame: 12 weeks]
• Patient reported outcomes on NRS [Time frame: 24 weeks]
• Patient reported outcomes on NRS [Time frame: 12 weeks]
• Quality of Life questionnaires [Time frame: 24 weeks]

Eligibility criteria

Inclusion criteria

• Men and women, ≥ 18 years of age, capable of understanding and signing an informed consent (including sufficient literacy and proficiency in the local language) and following the study procedures
• Patients with rheumatoid arthritis (RA) according to the 2010 American College of Rheumatology/European Alliance of Associations for Rheumatology (ACR/EULAR) classification criteria
• Ongoing conventional therapy with oral methotrexate (between ≥10mg and 25mg weekly) for ≥3 months with stable dosing, and clinical and laboratory tolerance of this treatment for at least 12 weeks
• CDAI > 2.8 + at least 1 clinically swollen joint (on 28-Joint count)
• Willingness to increase methotrexate dosing and change the route of administration according to study procedures

Exclusion criteria

• Inflammatory rheumatic diseases other than RA
• Ongoing or previous therapy with any biological DiseaseModifying Anti-Rheumatic Drug (bDMARDs) or targeted synthetic DMARDs (tsDMARDs) or conventional synthetic DMARDs (csDMARDs) other than methotrexate and hydroxychloroquine
• Use of GC unless on stable oral dose ≤10mg for at least 4 weeks prior to study inclusion
• Patients using NSAIDs, unless taken at a stable dose for ≥2 weeks prior to study inclusion
• Intraarticular GC treatment in the last 8 weeks
• Patients with significant and clinically relevant MTX-drug toxicity as judged by the investigator
• Elevated liver enzymes (aspartate transaminase (ASAT) and/or alanine transaminase (ALAT)), and/or alkaline phosphatase (AP), and/or gamma-glutamyl transferase (GGT) above 2x the upper limit normal (ULN)
• Reduced kidney function (glomerular filtration rate (GFR)<60)
• Haematologic abnormalities (grade 2 or 3: anaemia, leukopenia, thrombocytopenia)
• Stomatitis under the treatment with MTX
• Known history of recurrent/serious infections in the previous two months (such as, but not limited to, hepatitis, pneumonia, or pyelonephritis)
• A positive HBsAg and/or HCV test at screening visit
• Ongoing or recurring opportunistic infections (e.g., herpes zoster, cytomegalovirus, pneumocystis, aspergillosis, histoplasmosis, or mycobacteria) as judged by the investigator
• Women of childbearing potential without the use of adequate birth control measures (e.g., abstinence, oral contraceptives, intrauterine device, barrier method with spermicide, implantable or injectable contraceptives or surgical sterilization) and willing to continue this precaution for the duration of the study until 6 months after receiving the last medication
• Current signs or symptoms of severe, progressive or uncontrolled renal, hepatic, haematologic, gastrointestinal, endocrine, pulmonary, cardiac, neurologic, or cerebral disease, as judged by the investigator
• Being unable or unwilling to undergo multiple venepunctures because of poor tolerability or lack of sufficient venous access
• Being unwilling or unable to perform s.c injections
• Presence of a transplanted solid organ (with the exception of a corneal transplant > 3 months prior to screening)
• Women who are pregnant, nursing; or planning pregnancy during the study and 6 months after the individual study completion
• History of alcohol or substance abuse within the preceding 6 months
• Any medical or psychological condition that, judged by the investigator, would interfere with safe completion of the trial
• Immunisation with a live/attenuated vaccine within 12 weeks prior to baseline or potential need to receive a live vaccine during the course of the study
• Active participation in any other interventional study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Single blind

Primary purpose

Treatment

Study locations

Austria · 1 center

• Medical University of Vienna — Vienna

Identifiers

NCT: NCT06649136 · MethMax Trial

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗