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Arthritis, RheumatoidNCT06016517

Application of the Personalized N-of-1 Trial Design in Patients With Rheumatoid Arthritis

An observational study of Arthritis, Rheumatoid, run by Tufts Medical Center at 1 site in United States.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The goal of this N-of-1 study is to learn about treatment for individual patients who have rheumatoid arthritis (RA,) for which many treatments are available. The treatments are different in how they work, the way they are given, side- effects, and cost. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Arthritis, Rheumatoid
What is being tested?
Etanercept, Adalimumab and Upadacitinib
How many people
18 participants
Where
1 siteUnited States
Study dates
1 Sep 2026to 15 Dec 2028
Phase
Observational
Are there results?
Not yet: the study is under way

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
  • No healthy volunteers
  • Adult, Older adult

Study population: Outpatients 18 years of age or older with newly diagnosed RA following initial treatment with MTX, to which they are partial responders or non-responders.

In order to be eligible to participate in this study, a subject must meet all the following criteria:

  • Newly diagnosed adult-onset Rheumatoid Arthritis (RA) as defined by the American College of Rheumatology/ European League Against Rheumatism (ACR/EULAR) 2021 Criteria for the Classification of RA
  • Moderately to severely active RA defined as the presence of at least 6/68 tender joints and at least 6/66 swollen joints
  • C-reactive protein (CRP) or high-sensitivity C-reactive protein (hsCRP) measurement ≥ 1 time the upper limit of normal
  • First-line therapy with MTX for at least the 12 weeks prior to study entry with a continuous, non-changing dose for at least 8 weeks prior to study entry but continue to exhibit active RA
  • Had to discontinue MTX due to intolerability or toxicity, irrespective of treatment duration
  • Have never received etanercept, adalimumab, upadacitinib, or tocilizumab prior to first dose of study drug.
  • Provision of informed consent in English or another language in which a validated consent form is available, or via short-form consent with the assistance of a qualified interpreter.
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • 18 years of age or older
  • Ability to take oral medication and be willing to adhere to all treatment periods
  • Patients are eligible whether their disease responded partially or inadequately to first-line MTX or if they were intolerant to first-line MTX
  • Enrollment in an insurance plan that participates in or is subscribed to this trial

An individual who meets any of the following criteria will be excluded from participation in this study:

  • History of any arthritis with onset prior to age 17 years or current diagnosis of inflammatory joint disease other than RA
  • Has received intra-articular, intravenous, intramuscular corticosteroids within 28 days prior to baseline
  • Known allergic reactions to components of any of the investigative biologic agents
  • Is currently receiving corticosteroids at doses > (greater than) 10 mg per day of prednisone (or equivalent) or have been receiving an unstable dosing regimen of corticosteroids within 2 weeks of study entry or within 6 weeks of planned randomization
  • Has experienced any of the following within 12 weeks of study entry: myocardial infarction, unstable ischemic heart disease, stroke, or have New York Heart Association stage IV heart failure
  • Tuberculosis infection
  • Hepatitis B or C infection
  • History of venous thromboembolic event (deep vein thrombosis, pulmonary embolism)
  • Has a history or presence of cardiovascular, respiratory, hepatic, gastrointestinal, endocrine, hematological, neurological, or neuropsychiatric disorders or any other serious and/or unstable illness that, in the opinion of the investigator, could constitute a risk or could interfere with the interpretation of data
  • Has an estimated glomerular filtration rate (eGFR) based on the most recent available serum creatinine of < (less than) 40 milliliter per minute per 1.73 m^2 (mL/min/1.73 m^2)
  • Has a history of chronic liver disease with the most recent available aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >1.5 times the ULN or the most recent available total bilirubin ≥1.5 times the ULN
  • Has a history of, lymphoproliferative disease; or have signs or symptoms suggestive of possible lymphoproliferative disease, including lymphadenopathy or splenomegaly; or have active primary or recurrent malignant disease; or have been in remission from clinically significant malignancy for <5 years
  • Has been exposed to a live vaccine within 12 weeks prior to planned randomization or are expected to need/receive a live vaccine during the course of the study (with the exception of herpes zoster vaccination)
  • Has a current or recent clinically serious viral, bacterial, fungal, or parasitic infection
  • Has had symptomatic herpes zoster infection within 12 weeks prior to study entry
  • Has immunocompromising condition and, in the opinion of the investigator, are at an unacceptable risk for participating in the study and using these medications
  • Has a history of active hepatitis B virus (HBV), hepatitis C virus (HCV), or human immunodeficiency virus (HIV)*
  • Has evidence of active or latent tuberculosis (TB)
  • Current hospitalization or requiring hospital admission at screening
  • Pregnant or breastfeeding
  • Of childbearing potential, unwilling to use effective birth control method (highly effective contraceptive measure (e.g., combined (estrogen and progestogen containing) hormonal contraception; intrauterine device)
  • Participation in another therapeutic clinical trial for RA
  • Lack of internet access to telehealth platform

State who will determine eligibility. Note that those who are designated to determine eligibility must have appropriate training, expertise, and oversight, for example a physician PI or Co-I on a biomedical study: Eligibility will be determined by the appropriately trained and delegated physician investigator or physician Co- investigator.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Maple Goh, MBChB, MPH contact

8574139870

maple.goh@tuftsmedicine.org

United States1 site
  • Tufts Medical Center

    Boston, Massachusetts, 02111

Other trials in United States

About this study

The goal of this N-of-1 study is to learn about treatment for individual patients who have rheumatoid arthritis (RA,) for which many treatments are available. The treatments are different in how they work, the way they are given, side- effects, and cost. While treatment guidelines are available, finding the best treatment order of treatments is often based on physician choice. The main question this study aims to answer are:

  • What are the effects of different treatments on RA symptoms and condition for each individual patient
  • What is the effectiveness of different treatments across all patients enrolled in the N-of-1 study

Participants will be enrolled and randomized to a sequence of three U.S. Food and Drug Administration (FDA) approved RA medications: 1. etanercept, 2. adalimumab, 3. upadacitinib 4. tocilizumab. Participants will be asked to complete questionnaires about their condition and quality of life fortnightly, monthly and/or quarterly (either in clinic or remotely) and report their level of pain on alternate days (remotely).

Read the detailed description

Rheumatoid arthritis (RA) is a chronic, slowly progressive condition for which numerous treatment options are available. The therapies vary in mechanism of action, mode of administration, side- effect (adverse event) profile, and cost. While consensus treatment guidelines are available, identifying an optimal treatment sequence is often based on clinician choice with treatment changes based on tolerability and short- term outcome. The N-of-1 trial will evaluate individual participant and aggregate data.

Individual participants will be enrolled and randomized to a sequence of three U.S. Food and Drug Administration (FDA)-approved therapeutic agents etanercept, adalimumab, upadacitinib and tocilizumab.

The N-of-1- RA protocol describes patient allocation into a series of individual comparisons.

  • Patients with newly diagnosed rheumatoid arthritis following initial treatment with methotrexate (MTX). Participants will be allocated to:
  • MTX responder
  • MTX non- responder or partial responder

Eligible participants will either continue MTX or discontinue MTX, based on response to initial therapy and tolerance. Participants identified for subsequent biologic therapy will enter the biologic therapy phase of the study; with MTX either continued or not continued. This phase consists of a sequence of 4 therapeutic intervention regimens, each lasting 12-weeks.

The treatment conditions are as follows:

  1. Tumor Necrosis Factor (TNF) Inhibitor biologic: etanercept 50 mg subcutaneously weekly.

B: TNF- inhibitor biologic: Adalimumab 40 mg subcutaneously every 2 weeks. C. Janus Kinase (JAK) Inhibitor: Upadacitinib 15 mg orally once daily. D. Interleukin 6 (IL-6) Inhibitor: Tocilizumab 162 mg administered SQ every 2 weeks (if there is an inadequate response to prior three biologics).

Primary Objective (individual N-of-1 trial): To generate randomized evidence about the effects of therapeutic agents on RA symptoms and disease activity to inform decision about best treatment at the end of the trial period for each participant.

Secondary Objective (aggregation of the series of N-of-1 trials): To evaluate the average relative effectiveness of therapeutic agents across all participants and explore heterogeneity of treatment effects.

For the aggregated series of N-of-1 trial, we will use the following hierarchy of endpoints.

Primary Endpoint:

  • DAS28 (CRP and ESR)

Secondary Endpoints:

  • American College of Rheumatology 20% (ACR20), 50% (ACR50) and 70% (ACR70) response
  • Routine Assessment of Patient Index Data (RAPID3) score based on participants' report of overall assessment of the disease, the level of pain, and the amount of physical disability
  • Short Form 12-Item Health Survey (SF-12) measuring the impact of disease on overall quality of life during the prior 4 weeks (physical function, pain, general and mental health, vitality, social function, physical and emotional health)
  • Report of worst pain and effect of pain on function (0-10) every other day
  • Treatment Burden Questionnaire (TBQ) administered at the end of each treatment condition

Safety Endpoint(s):

  • Number (and proportion) of patients reporting treatment emergent adverse events (TEAEs) (by MedDRA system organ class and preferred term)

For each individual N-of-1 trial, we will use the endpoints listed above, but without any pre-specified hierarchy, assuming that each patient will identify endpoints most important to them.

Being tested
Etanercept, Adalimumab, Upadacitinib, Tocilizumab
Medical subject headings
Arthritis, Rheumatoid

What participants receive

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

  • EtanerceptDrug

    Also called Enbrel

    50 mg subcutaneously weekly

  • AdalimumabDrug

    Also called Humira

    40 mg subcutaneously every 2 weeks

  • UpadacitinibDrug

    Also called Rinvoq

    15 mg orally once daily with subcutaneous placebo injection every 2 weeks

  • TocilizumabDrug

    162 mg administered SQ every 2 weeks

What is being measured

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

  1. Change in Disease Activity Score (DAS) 28

    Evaluates patient and physician overall assessment of disease activity, including the number of swollen and painful joints (out of 28 joints),

    Measured: Baseline and week 12 of each treatment period

Secondary outcomes (6)
  1. Change in The Routine Assessment of Patient Index Data 3 (RAPID3)

    Assessment of a) function, b) pain, and c) patient global estimate of status

    Measured: Baseline, and weeks 2, 4, 6, 8, 10, 12 of each treatment period

  2. Change in American College of Rheumatology 20 (ACR20)

    ≥20% fewer tender and swollen joints and ≥20% improvement in three of five other domains; a) patient global assessment, b) physician global assessment, c) functional questionnaire, d) pain score, and f) erythrocyte sedimentation rate (ESR) or C-reactive protein (CRP)

    Measured: Baseline and week 12 of each treatment period

  3. Change in American College of Rheumatology 50 (ACR50)

    ≥50% fewer tender and swollen joints and ≥20% improvement in three of five other domains; a) patient global assessment, b) physician global assessment, c) functional questionnaire, d) pain score, and f) erythrocyte sedimentation rate (ESR) or C-reactive protein (CRP)

    Measured: Baseline and at week 12 of each treatment period

  4. Change in American College of Rheumatology 70 (ACR70)

    ≥70% fewer tender and swollen joints and ≥20% improvement in three of five other domains; a) patient global assessment, b) physician global assessment, c) functional questionnaire, d) pain score, and f) erythrocyte sedimentation rate (ESR) or C-reactive protein (CRP)

    Measured: Baseline and at week 12 of each treatment period

  5. The Medical Outcome Study Short-Form 12- item Health Survey (SF-12)

    General Health Questionnaire

    Measured: Baseline and at week 4, 8, and 12 of each treatment period

  6. Treatment Burden Questionnaire (TBQ)

    Assessment of the burden associated with taking medicine, self-monitoring, laboratory tests, doctor visits, need for organization, administrative tasks, following advice on diet and physical activity, and social impact of treatment.

    Measured: At week 36

Timeline

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

  1. First posted29 Aug 2023
  2. Study start1 Sep 2026 (estimated)
  3. Primary completion1 Sep 2028 (estimated)
  4. Study completion15 Dec 2028 (estimated)

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
18 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06016517
Sponsor's protocol ID
00003917
Status last verified
Jul 2026
First submitted
26 Jun 2023
Last updated
22 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Arthritis, Rheumatoid, run by Tufts Medical Center at 1 site in United States.

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

Who may be eligible to take part?

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: opening soon, as of the sponsor's last update on 22 Jul 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 United States. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Maple Goh, MBChB, MPH (8574139870, maple.goh@tuftsmedicine.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Disease Activity Score (DAS) 28 (time frame: Baseline and week 12 of each treatment period). 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 22 Jul 2026.

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