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Rheumatoid ArthritisMARAJANCT04530305

Microbiota Analysis to Predict Outcomes of Rheumatoid Arthritis Patients Treated With JAK-inhibitor

An observational study of Rheumatoid Arthritis, run by University Hospital, Montpellier at 1 site in France.

Suspended

Paused. Enrolment is on hold for now and may resume.

Official record
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Trial summary

Personalized medicine in which each patient would receive the ideal personalized treatment and regimen, holds great promise to improve patient's care. However, previous studies failed to establish validated predictors of response to disease-modifying anti-rheumatic drugs (DMARDs) in patients with rheumatoid arthritis… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Rheumatoid Arthritis
What is being tested?
Upadacitinib <15 MG [Rinvoq]
How many people
60 participants
Where
1 siteFrance
Study dates
7 Jan 2021to 16 May 2027
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Adult, Older adult

Study population: Patients with RA fulfilling American College of Rheumatology (ACR)/ European league against rheumatism (EULAR) 2010 criteria with inadequate response to MTX for who a treatment with UPA will be prescribed in standard care to control disease activity

Who may be able to join

  • Patients with RA fulfilling American College of Rheumatology (ACR)/ European league against rheumatism (EULAR) 2010 criteria
  • Patients with inadequate response to MTX
  • Patients receiving MTX as adjuvant therapy or will receive UPA as monotherapy

Who cannot join

  • Patients with contraindication to upadacitinib
  • Patients previously treated with biological DMARDs or JAK inhibitors
  • Patients treated with ≥ 10 mg/day of glucocorticoids
  • Use of IV glucocorticoids in the previous month
  • Previous use of biological DMARDs (TNF inhibitors, rituximab, abatacept, tocilizumab) or JAK inhibitors
  • Absence of informed consent
  • Pregnancy planned for the duration of the study, Women pregnant or breastfeeding women
  • Major protected by law or patient under guardianship

Trial locations and contacts

1 site in 1 country.

France1 site
  • CHU de Montpellier

    Montpellier, 34295

Other trials in France

About this study

Personalized medicine in which each patient would receive the ideal personalized treatment and regimen, holds great promise to improve patient's care. However, previous studies failed to establish validated predictors of response to disease-modifying anti-rheumatic drugs (DMARDs) in patients with rheumatoid arthritis (RA). JAK inhibitors is a new class of DMARDs with great efficacy that might be even superior to anti-TNF drugs. As there are chemicals, their production cost is much cheaper than biological therapies and they will probably be central in patient's care in the coming years. Three are currently available: upadacitinib (UPA) tofacitinib and baricitinib. Our study will focus on UPA. Clinical outcomes mainly depend on i) factors influencing drug metabolism \& concentrations and ii) adequacy between drug target and the inflammation pathways involved in the patient's disease. Humans carry in their gut trillions of germs, which are now known to be key players in health and disease. Those germs possess many enzymes and strongly modulate human enzymes expression. Gut-microbiota can, indeed, directly metabolize oral drugs and control the expression of the cytochrome P450 3A4 (CYP3A4), the main enzyme metabolizing TOFA. We showed, in a preliminary mouse experiment, that modifying gut-microbiota composition changes JAKi effects on signaling pathways. We thus believe that models including gut-microbiota composition together with markers of immune activation will predict clinical outcomes in RA patients treated with UPA.

Main and secondary objectives: To build predictive models for clinical outcomes (efficacy and safety) of RA patients treated with UPA based on microbiota analysis and markers f immune activation.

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Methodolgy:

This multicentric longitudinal prospective study will include 60 patients with RA and inadequate response to methotrexate. The clinical outcomes studied will be EULAR non-response at 3 months as defined by the European league against rheumatism EULAR (primary outcome), achievement of low-disease activity at 6 months or incident adverse events (secondary outcomes). Gut microbiota will be assessed at baseline and M3 from thawed fecal samples. DNA will be purified using QIAamp DNA stool mini kit (Qiagen) and qualify using Qubit and TapeStation 4200 (Agilent). Library will be prepared by amplification of V1-V2 and V3-V4 regions from the bacterial 16S rRNA genes and will be qualified by q-PCR and amplicons will be sequenced by MiSeq (Illumina). Initial bioinformatic analysis and taxonomies will be carried out using the QIIME2 software. Immune activation will be assessed through JAK-STAT pathway activation by JAK STAT signaling pathway RT² profiler PCR Array (Qiagen) which profiles expression of 84 genes related to Jak and Stat-mediated signaling. UPA concentrations will be assessed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) at baseline and 3 months. Statistical classifiers (Neural network algorithm, Linear and Quadratic Discriminant Analysis, Support Vector Machine, Random forests, Shrinkage Methods, or Nearest Neighbors) incorporating microbiome, JAK STAT signaling pathway gene expression and clinical data, will be used to determine profiles associated with UPA clinical response and safety. Patients who will prematurely stop UPA (before 3 months) for adverse events or loss of follow-up will be considered as non-responders.

Read the detailed description

Gut microbiota is becoming an important predictor of response and tolerance with anti-cancer drugs. However, its potential of prediction in other fields has poorly been explored.

Drug metabolism and concentrations of tofacitinib depend on body mass index, liver function and cytochrome P450 activity (especially CYP3A4). Humans carry in their gut trillions of germs, which are now known to be key players in health and disease. Those germs can strongly impact drug metabolism and concentrations based on 3 mechanisms. First, gut bacteria possess a huge pool of enzymes which catalyzes drug metabolism reactions. Second, gut microbiota regulates bile acid metabolism which play critical role in drug metabolism. Third, gut microbiota modulates the expression of cytochrome P450, especially CYP3A4, the main enzyme catabolizing Tofacitinib (TOFA).

In addition to drug metabolism, gut microbiota is a key driver of immune activation. Clinical response to CTLA-4 or anti-PD-1 strongly depends on gut microbiota in different cancers. The experiments performed to decipher the mechanisms involved suggested that microbiota composition affects immune responses, which will facilitate or not anti-tumoral efficacy of checkpoints inhibitors.

RA is a heterogeneous disease with predominant inflammation pathways varying dependent on patients. Some RA seem to be more dependent on IL-6 whereas others rely more on TNF-alpha, B or T cells. Gut microbiota was shown to affect all those different targets. Assessing baseline levels of JAK STAT signaling pathway gene expression will help us to link immune activation, gut microbiota and clinical response to UPA.

We hypothesize that gut-microbiota composition impacts JAKi metabolism, immune activation, and thus clinical response and has a great potential to predict clinical outcomes in patients with RA treated with UPA.

Study objectives :

  1. Main objective To construct a model based on gut-microbiota composition, immune activation markers (JAK-STAT signalling pathway) and clinical data to predict UPA non-response at 3 months in RA patients with inadequate response to methotrexate.
  2. Secondary objectives
  • To construct a model based on gut-microbiota composition, immune activation markers (JAK-STAT signalling pathway) and clinical data to predict low-disease activity at 6 months of UPA in RA patients with inadequate response to methotrexate.
  • To compare responders and non-responders and patients with or without adverse effects on UPA in terms of:
  • baseline gut-microbiota
  • UPA concentrations at 3 months
  • baseline JAK-STAT signalling pathway gene expression profile
  • baseline clinical data
  • To correlate changes in disease activity score based on 28 joint evaluation (DAS28, see annex for calculation) between month-3 and baseline with:
  • changes in gut microbiota
  • UPA concentrations
  • changes in JAK-STAT signaling
Being tested
Upadacitinib <15 MG [Rinvoq]
Medical subject headings
Arthritis, Rheumatoid

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Upadacitinib <15 MG [Rinvoq]Drug

    Patients with RA for who the introduction of upadacitinib has been decided will be proposed the study. If they accept, they will be followed for 6 months with 3 visits (baseline, 3 and 6 months) which is the usual standard care. In addition to routine markers, stool and blood will be collected at baseline and 3 months specifically for the study.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. EULAR response

    Response will be defined following European league against rheumatism EULAR definition that is a decrease >0.6 points of Disease-Activity-Score 28-joints (DAS28-CRP) and a DAS28-CRP≤5.1 at 3 months . Patients who will prematurely stop UPA (before 3 months) for adverse events, RA flair or loss of follow-up will be considered as non-responders.

    Measured: 3 months

Secondary outcomes (7)
  1. EULAR good response

    EULAR good-response at 3 and 6 months: DAS28-CRP≤3.2 and deltaDAS28 (M0-M3)>1.2

    Measured: 3 and 6 months

  2. Achievement of low-disease activity:

    DAS28-CRP at 6 months <3.2 and/or DAS28-ESR at 6 months <3.2

    Measured: 6 months

  3. Adverse events

    Incidence, relatedness, and severity of treatment-emergent SUSARs, SAEs, ARs and AEs will be evaluated continuously. Patients with adverse events occurring between study visits will be asked to contact the study center for AE reporting.

    Measured: during the 6 month follow-up

  4. Baseline gut-microbiota

    microbiota will be described in terms of alpha and beta diversity, phylum, genus, OTU.

    Measured: baseline, 3 and 6 months

  5. UPA concentrations

    Measured: 0, 3 and 6 months

  6. Baseline JAK-STAT signalling pathway gene expression profile

    gene expression profile will include the level of expression of 84 genes

    Measured: baseline

  7. Baseline clinical data

    DAS28-CRP, body-mass index, age and gender

    Measured: baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Aug 2020
  2. Study start7 Jan 2021
  3. Primary completion16 Sep 2026
  4. Study completion16 May 2027 (estimated)

Why it stopped: Evolution of treatment sequencing for JAK inhibitors

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04530305
Sponsor's protocol ID
RECHMPL19_0224
Acronym
MARAJA
Status last verified
Oct 2026
First submitted
24 Aug 2020
Last updated
26 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Rheumatoid Arthritis, run by University Hospital, Montpellier at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: paused, as of the sponsor's last update on 26 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

EULAR response (time frame: 3 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Oct 2026.

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