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Study to Determine the Effects of Different Doses of Methotrexate (MTX) When Taken With Adalimumab in Subjects With Early Rheumatoid Arthritis (RA)

A Double-Blind, Randomized, Parallel-Arm, Multicenter Study to Determine the Dose Response of Methotrexate (MTX) in Combination Therapy With Adalimumab in Subjects With Early Rheumatoid Arthritis (CONCERTO)

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01185301
Acronym
CONCERTO
Enrollment
395
Registered
2010-08-19
Start date
2010-10-31
Completion date
2012-09-30
Last updated
2013-11-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Early Rheumatoid Arthritis

Keywords

Arthritis, Erosion, Humira, Adalimumab, Injection, Rheumatoid, Methotrexate

Brief summary

The purpose of this study is to determine the effects of different doses of methotrexate (MTX) when taken with adalimumab in subjects with early rheumatoid arthritis (RA).

Interventions

BIOLOGICALadalimumab

Pre-filled syringe every other week

DRUGmethotrexate

weekly oral capsule dosing

Sponsors

AbbVie (prior sponsor, Abbott)
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male and female subjects at least 18 years of age * Subject has a diagnosis of Rheumatoid Arthritis (RA) as defined by either the 1987-revised American College of Rheumatology (ACR) classification criteria or the new ACR/ European League Against Rheumatism (EULAR) diagnostic criteria for RA 2010 and has a disease duration of less than 1 year from diagnosis by a licensed health care provider * Subject must meet the following criteria: 1. Disease Activity Score of C-reactive Protein (DAS28\[CRP\]) ≥ 3.2 (at the Baseline visit only) 2. At least 6 swollen joints out of 66 assessed (at the Screening and Baseline visits) 3. At least 8 tender joints out of 68 assessed (at the Screening and Baseline visits) 4. C-reactive protein (CRP) ≥ 1.5 mg/dL (at the Screening visit only), or erythrocyte sedimentation rate (ESR) ≥ 28 mm/1h (at the Screening and Baseline visits) 5. Fulfill at least one of the following three criteria: Rheumatoid Factor (RF) positive, have at least 1 bony erosion, anti-cyclic citrullinated peptide (anti-CCP) antibody positive * Subject is judged to be in good health as determined by the Principal Investigator based upon the results of medical history, laboratory profile, physical examination, chest x-ray (CXR), and a 12-lead electrocardiogram (ECG) performed during Screening

Exclusion criteria

* Subject has previous exposure to any systemic biologic therapy including adalimumab * Subject has been previously treated with greater than 1 disease modifying antirheumatic drugs (DMARDs) or with methotrexate (MTX) * Subject has undergone joint surgery within the preceding two months (at joints to be assessed within the study) * Subject has chronic arthritis diagnosed before age 17 years * History of invasive infection (e.g., listeriosis and histoplasmosis), chronic or active Hepatitis C infection, human immunodeficiency virus (HIV) infection, immunodeficiency syndrome, chronic recurring infections or active tuberculosis (TB) * Hepatitis B virus: hepatitis B surface antigen (HBs Ag) positive (+) or detected sensitivity on the hepatitis B virus DNA (HBV DNA) polymerase chain reaction (PCR) qualitative test * Infection(s) requiring treatment with intravenous (IV) anti-infectives within 30 days prior to the Baseline Visit or oral anti-infectives within 14 days prior to the Baseline visit * Female subject who is pregnant or breast-feeding or considering becoming pregnant

Design outcomes

Primary

MeasureTime frameDescription
Percentage of Participants With 28-Joint Disease Activity Score of C-reactive Protein (DAS28[CRP]) Low Disease Activity at Week 26Week 26Percentage of participants achieving low disease activity as defined by a clinical response (DAS28\[CRP\] \< 3.2). The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, C-reactive protein, and general health are included in the DAS28 score. Scores on the DAS28 range from 0 to 10. A DAS28 score \>5.1 indicates high disease activity, a DAS28 score \<3.2 indicates low disease activity, and a DAS28 score \<2.6 indicates clinical remission.

Secondary

MeasureTime frameDescription
Percentage of Participants With American College of Rheumatology (ACR) 20 Criteria Response at Week 26Baseline, Week 26Response, as defined by ACR 20 criteria at Week 26. A participant is a responder if the following 3 criteria for improvement from Baseline are met: ≥ 20% improvement in tender joint count; ≥ 20% improvement in swollen joint count; and ≥ 20% improvement in at least 3 of the 5 following parameters: * Physician global assessment of disease activity * Patient global assessment of disease activity * Patient assessment of pain * Disability Index of the Health Assessment Questionnaire * Acute phase reactant value (C-reactive protein).
Percentage of Participants With American College of Rheumatology (ACR) 50 Criteria Response at Week 26Baseline, Week 26Response, as defined by ACR 50 criteria at Week 26. A participant is a responder if the following 3 criteria for improvement from Baseline are met: ≥ 50% improvement in tender joint count; ≥ 50% improvement in swollen joint count; and ≥ 50% improvement in at least 3 of the 5 following parameters: * Physician global assessment of disease activity * Patient global assessment of disease activity * Patient assessment of pain * Disability Index of the Health Assessment Questionnaire * Acute phase reactant value (C-reactive protein).
Percentage of Participants With American College of Rheumatology (ACR) 70 Criteria Response at Week 26Baseline, Week 26Response, as defined by ACR 70 criteria at Week 26. A participant is a responder if the following 3 criteria for improvement from Baseline are met: ≥ 70% improvement in tender joint count; ≥ 70% improvement in swollen joint count; and ≥ 70% improvement in at least 3 of the 5 following parameters: * Physician global assessment of disease activity * Patient global assessment of disease activity * Patient assessment of pain * Disability Index of the Health Assessment Questionnaire * Acute phase reactant value (C-reactive protein).
Percentage of Participants With American College of Rheumatology (ACR) 90 Criteria Response at Week 26Baseline, Week 26Response, as defined by ACR 90 criteria at Week 26. A participant is a responder if the following 3 criteria for improvement from Baseline are met: ≥ 90% improvement in tender joint count; ≥ 90% improvement in swollen joint count; and ≥ 90% improvement in at least 3 of the 5 following parameters: * Physician global assessment of disease activity * Patient global assessment of disease activity * Patient assessment of pain * Disability Index of the Health Assessment Questionnaire * Acute phase reactant value (C-reactive protein).
Percentage of Participants With American College of Rheumatology (ACR) 100 Criteria Response at Week 26Baseline, Week 26Response, as defined by ACR 100 criteria at Week 26. A participant is a responder if the following 3 criteria for improvement from Baseline are met: ≥ 100% improvement in tender joint count; ≥ 100% improvement in swollen joint count; and ≥ 100% improvement in at least 3 of the 5 following parameters: * Physician global assessment of disease activity * Patient global assessment of disease activity * Patient assessment of pain * Disability Index of the Health Assessment Questionnaire * Acute phase reactant value (C-reactive protein).
Percentage of Participants With DAS28(CRP) Remission at Week 26Week 26Disease remission was defined as a disease activity score, based on CRP, for 28 joints that was \< 2.6 (DAS28\[CRP\] \< 2.6). The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, C-reactive protein, and general health are included in the DAS28 score. Scores on the DAS28 range from 0 to 10.
Percentage of Participants With a Change From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) ≤ -0.22 at Week 26Baseline, Week 26The Health Assessment Questionnaire - Disability Index is a patient-reported questionnaire specific for rheumatoid arthritis. It consists of 20 questions referring to eight domains: dressing/grooming, arising, eating, walking, hygiene, reach, grip, and daily activities. Participants assessed their ability to do each task over the past week using the following response categories: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). Scores on each task were summed and averaged to provide an overall score ranging from 0 to 3, where zero represents no disability and three very severe, high-dependency disability. The minimal clinically important difference (MCID) defined for the HAQ-DI is a change from Baseline of ≥ 0.22. HAQ remission indicating normal physical function is defined by HAQ-DI score of \< 0.5. Negative change from Baseline in the overall score indicates improvement.
Change From Baseline in Modified Total Sharp Score (mTSS) at Week 26Baseline, Week 26The modified Total Sharp Score (mTSS) is a measure of change in joint health from digitized images of radiographs of hands and feet. Joints were scored for erosions on a scale of 0 (no damage) to 5 (complete collapse) and joint space narrowing on a scale of 0 (no damage) to 4 (ankylosis or complete dislocation). Erosion scores and narrowing scores were added to obtain the mTSS (range = 0 \[normal\] to 398 \[maximal disease\]). An increase in mTSS from Baseline represents disease progression and/or joint worsening, no change represents halting of disease progression, and a decrease represents improvement.
Percentage of Participants With No Radiographic Progression at Week 26Baseline, Week 26No radiographic progression was defined as a change from Baseline in modified Total Sharp Score (mTSS) at Week 26 of ≤ 0.5. mTSS is a measure of change in joint health from digitized images of radiographs of hands and feet. Joints were scored for erosions on a scale of 0 (no damage) to 5 (complete collapse) and joint space narrowing on a scale of 0 (no damage) to 4 (ankylosis or complete dislocation). Erosion scores and narrowing scores were added to obtain the mTSS (range = 0 \[normal\] to 398 \[maximal disease\]). An increase in mTSS from Baseline represents disease progression and/or joint worsening, no change represents halting of disease progression, and a decrease represents improvement.
Percentage of Participants With Simplified Disease Activity Index (SDAI) Remission at Week 26Week 26SDAI is a measure of disease activity derived as follows: SDAI = SJC28 + TJC28 + GH (cm) + PhGA (cm) + CRP (mg/dL), where TJC28 and SJC28 represent total tender joint count and total swollen joint count, respectively, based on 28 joints (including the left and right side of the body), GH = Patient's Global Assessment of Disease Activity, and PhGA = Physician's Global Assessment of Disease Activity (both measured on a visual analogue scale with a range of 0 \[none\] to 10 \[severe\]), and CRP is C-reactive protein measured in mg/dL. SDAI total score = 0 to 86. SDAI ≤ 3.3 indicates disease remission, \> 3.4 to 11 = low disease activity, \> 11 to 26 = moderate disease activity, and \> 26 = high disease activity.
Percentage of Participants With Clinical Disease Activity Index (CDAI) Remission at Week 26Week 26CDAI is a measure of disease activity derived as follows: CDAI = SJC28 + TJC28 + GH (cm) + PhGA (cm) where TJC28 and SJC28 represent total tender joint count and total swollen joint count, respectively, based on 28 joints (including the left and right side of the body), GH = Patient's Global Assessment of Disease Activity, and PhGA = Physician's Global Assessment of Disease Activity (both measured on a visual analogue scale with a range of 0 \[none\] to 10 \[severe\]). CDAI total score = 0 to 76. CDAI ≤ 2.8 indicates disease remission, \> 2.8 to 10 = low disease activity, \> 10 to 22 = moderate disease activity, and \> 22 = high disease activity.
Change From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) Score at Week 26Baseline, Week 26The Health Assessment Questionnaire - Disability Index (HAQ-DI) is a patient-reported questionnaire specific for rheumatoid arthritis. It consists of 20 questions referring to 8 domains: dressing/grooming, arising, eating, walking, hygiene, reach, grip, and daily activities. Participants assessed their ability to do each task over the past week using the following response categories: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). Scores on each task were summed and averaged to provide an overall score ranging from 0 to 3, where 0 represents no disability and 3 very severe, high-dependency disability. HAQ remission indicating normal physical function is defined by HAQ-DI score of \< 0.5. Negative change from Baseline in the overall score indicates improvement.

Countries

Argentina, Austria, Belgium, Canada, Czechia, Germany, Poland, Puerto Rico, Spain, United States

Participant flow

Participants by arm

ArmCount
ADA + 2.5 mg MTX
2.5 mg methotrexate (MTX) oral capsule weekly with 40 mg adalimumab (ADA) subcutaneous (SC) injection every other week (EOW) for 26 weeks
98
ADA + 5 mg MTX
5 mg MTX oral capsule weekly with 40 mg ADA SC injection EOW for 26 weeks
100
ADA + 10 mg MTX
10 mg MTX oral capsule weekly with 40 mg ADA SC injection EOW for 26 weeks
99
ADA + 20 mg MTX
MTX oral capsule dose escalation from 10 mg to 20 mg in 2.5 mg increments every other week (10 mg x 2 weeks, 12.5 mg x 2 weeks, 15 mg x 2 weeks, 17.5 mg x 2 weeks), then 20 mg for 18 weeks with 40 mg ADA SC injection EOW for 26 weeks
98
Total395

Withdrawals & dropouts

PeriodReasonFG000FG001FG002FG003
Overall StudyAdverse Event3023
Overall StudyLost to Follow-up2001
Overall StudyOther Reason3222
Overall StudyWithdrawal by Subject7523

Baseline characteristics

CharacteristicADA + 2.5 mg MTXTotalADA + 20 mg MTXADA + 10 mg MTXADA + 5 mg MTX
28-Joint Disease Activity Score of C-reactive Protein (DAS28[CRP])6.10 scores on a scale
STANDARD_DEVIATION 0.921
6.02 scores on a scale
STANDARD_DEVIATION 0.97
5.91 scores on a scale
STANDARD_DEVIATION 1.014
5.86 scores on a scale
STANDARD_DEVIATION 0.971
6.22 scores on a scale
STANDARD_DEVIATION 0.943
Age Continuous52.0 years
STANDARD_DEVIATION 13.19
51.9 years
STANDARD_DEVIATION 13.46
53.8 years
STANDARD_DEVIATION 14.41
52.1 years
STANDARD_DEVIATION 12.94
49.7 years
STANDARD_DEVIATION 13.14
Age, Customized
< 65 years
84 participants335 participants77 participants85 participants89 participants
Age, Customized
> 65 years
14 participants60 participants21 participants14 participants11 participants
Health Assessment Questionnaire - Disability Index (HAQ-DI)1.49 units on a scale
STANDARD_DEVIATION 0.737
1.57 units on a scale
STANDARD_DEVIATION 0.67
1.58 units on a scale
STANDARD_DEVIATION 0.653
1.62 units on a scale
STANDARD_DEVIATION 0.667
1.57 units on a scale
STANDARD_DEVIATION 0.624
Modified Total Sharp Score (mTSS)9.79 score
STANDARD_DEVIATION 12.849
9.92 score
STANDARD_DEVIATION 12.005
10.55 score
STANDARD_DEVIATION 12.852
10.76 score
STANDARD_DEVIATION 13.017
8.60 score
STANDARD_DEVIATION 8.912
Sex: Female, Male
Female
70 Participants300 Participants74 Participants78 Participants78 Participants
Sex: Female, Male
Male
28 Participants95 Participants24 Participants21 Participants22 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
— / —— / —— / —— / —
other
Total, other adverse events
24 / 9826 / 10034 / 9941 / 98
serious
Total, serious adverse events
5 / 982 / 1003 / 997 / 98

Outcome results

Primary

Percentage of Participants With 28-Joint Disease Activity Score of C-reactive Protein (DAS28[CRP]) Low Disease Activity at Week 26

Percentage of participants achieving low disease activity as defined by a clinical response (DAS28\[CRP\] \< 3.2). The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, C-reactive protein, and general health are included in the DAS28 score. Scores on the DAS28 range from 0 to 10. A DAS28 score \>5.1 indicates high disease activity, a DAS28 score \<3.2 indicates low disease activity, and a DAS28 score \<2.6 indicates clinical remission.

Time frame: Week 26

Population: Intent-to-Treat population; participants with a missing response were imputed as non-responders.

ArmMeasureValue (NUMBER)
ADA + 2.5 mg MTXPercentage of Participants With 28-Joint Disease Activity Score of C-reactive Protein (DAS28[CRP]) Low Disease Activity at Week 2642.9 percentage of participants
ADA + 5 mg MTXPercentage of Participants With 28-Joint Disease Activity Score of C-reactive Protein (DAS28[CRP]) Low Disease Activity at Week 2644.0 percentage of participants
ADA + 10 mg MTXPercentage of Participants With 28-Joint Disease Activity Score of C-reactive Protein (DAS28[CRP]) Low Disease Activity at Week 2656.6 percentage of participants
ADA + 20 mg MTXPercentage of Participants With 28-Joint Disease Activity Score of C-reactive Protein (DAS28[CRP]) Low Disease Activity at Week 2660.2 percentage of participants
Secondary

Change From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) Score at Week 26

The Health Assessment Questionnaire - Disability Index (HAQ-DI) is a patient-reported questionnaire specific for rheumatoid arthritis. It consists of 20 questions referring to 8 domains: dressing/grooming, arising, eating, walking, hygiene, reach, grip, and daily activities. Participants assessed their ability to do each task over the past week using the following response categories: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). Scores on each task were summed and averaged to provide an overall score ranging from 0 to 3, where 0 represents no disability and 3 very severe, high-dependency disability. HAQ remission indicating normal physical function is defined by HAQ-DI score of \< 0.5. Negative change from Baseline in the overall score indicates improvement.

Time frame: Baseline, Week 26

Population: Intent-to-Treat population with non-missing baseline and at least 1 non-missing post-baseline value (baseline is defined as the last non-missing value prior to the first dose of study drug); last observation carried forward.

ArmMeasureValue (MEAN)Dispersion
ADA + 2.5 mg MTXChange From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) Score at Week 26-0.72 units on a scaleStandard Deviation 0.664
ADA + 5 mg MTXChange From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) Score at Week 26-0.71 units on a scaleStandard Deviation 0.717
ADA + 10 mg MTXChange From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) Score at Week 26-0.78 units on a scaleStandard Deviation 0.647
ADA + 20 mg MTXChange From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) Score at Week 26-0.82 units on a scaleStandard Deviation 0.698
Secondary

Change From Baseline in Modified Total Sharp Score (mTSS) at Week 26

The modified Total Sharp Score (mTSS) is a measure of change in joint health from digitized images of radiographs of hands and feet. Joints were scored for erosions on a scale of 0 (no damage) to 5 (complete collapse) and joint space narrowing on a scale of 0 (no damage) to 4 (ankylosis or complete dislocation). Erosion scores and narrowing scores were added to obtain the mTSS (range = 0 \[normal\] to 398 \[maximal disease\]). An increase in mTSS from Baseline represents disease progression and/or joint worsening, no change represents halting of disease progression, and a decrease represents improvement.

Time frame: Baseline, Week 26

Population: Intent-to-Treat population with available data at time point (observed cases).

ArmMeasureValue (MEAN)Dispersion
ADA + 2.5 mg MTXChange From Baseline in Modified Total Sharp Score (mTSS) at Week 260.9 score on a scaleStandard Deviation 5.62
ADA + 5 mg MTXChange From Baseline in Modified Total Sharp Score (mTSS) at Week 260.3 score on a scaleStandard Deviation 1.92
ADA + 10 mg MTXChange From Baseline in Modified Total Sharp Score (mTSS) at Week 260.4 score on a scaleStandard Deviation 3.17
ADA + 20 mg MTXChange From Baseline in Modified Total Sharp Score (mTSS) at Week 260.2 score on a scaleStandard Deviation 2.22
Secondary

Percentage of Participants With a Change From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) ≤ -0.22 at Week 26

The Health Assessment Questionnaire - Disability Index is a patient-reported questionnaire specific for rheumatoid arthritis. It consists of 20 questions referring to eight domains: dressing/grooming, arising, eating, walking, hygiene, reach, grip, and daily activities. Participants assessed their ability to do each task over the past week using the following response categories: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). Scores on each task were summed and averaged to provide an overall score ranging from 0 to 3, where zero represents no disability and three very severe, high-dependency disability. The minimal clinically important difference (MCID) defined for the HAQ-DI is a change from Baseline of ≥ 0.22. HAQ remission indicating normal physical function is defined by HAQ-DI score of \< 0.5. Negative change from Baseline in the overall score indicates improvement.

Time frame: Baseline, Week 26

Population: Intent-to-Treat population; participants with a missing response were imputed as non-responders.

ArmMeasureValue (NUMBER)
ADA + 2.5 mg MTXPercentage of Participants With a Change From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) ≤ -0.22 at Week 2668.4 percentage of participants
ADA + 5 mg MTXPercentage of Participants With a Change From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) ≤ -0.22 at Week 2670.0 percentage of participants
ADA + 10 mg MTXPercentage of Participants With a Change From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) ≤ -0.22 at Week 2673.7 percentage of participants
ADA + 20 mg MTXPercentage of Participants With a Change From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) ≤ -0.22 at Week 2677.6 percentage of participants
Secondary

Percentage of Participants With American College of Rheumatology (ACR) 100 Criteria Response at Week 26

Response, as defined by ACR 100 criteria at Week 26. A participant is a responder if the following 3 criteria for improvement from Baseline are met: ≥ 100% improvement in tender joint count; ≥ 100% improvement in swollen joint count; and ≥ 100% improvement in at least 3 of the 5 following parameters: * Physician global assessment of disease activity * Patient global assessment of disease activity * Patient assessment of pain * Disability Index of the Health Assessment Questionnaire * Acute phase reactant value (C-reactive protein).

Time frame: Baseline, Week 26

Population: Intent-to-Treat population; participants with a missing response were imputed as non-responders.

ArmMeasureValue (NUMBER)
ADA + 2.5 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 100 Criteria Response at Week 261.0 percentage of participants
ADA + 5 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 100 Criteria Response at Week 261.0 percentage of participants
ADA + 10 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 100 Criteria Response at Week 262.0 percentage of participants
ADA + 20 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 100 Criteria Response at Week 264.1 percentage of participants
Secondary

Percentage of Participants With American College of Rheumatology (ACR) 20 Criteria Response at Week 26

Response, as defined by ACR 20 criteria at Week 26. A participant is a responder if the following 3 criteria for improvement from Baseline are met: ≥ 20% improvement in tender joint count; ≥ 20% improvement in swollen joint count; and ≥ 20% improvement in at least 3 of the 5 following parameters: * Physician global assessment of disease activity * Patient global assessment of disease activity * Patient assessment of pain * Disability Index of the Health Assessment Questionnaire * Acute phase reactant value (C-reactive protein).

Time frame: Baseline, Week 26

Population: Intent-to-Treat population; participants with a missing response were imputed as non-responders.

ArmMeasureValue (NUMBER)
ADA + 2.5 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 20 Criteria Response at Week 2667.3 percentage of participants
ADA + 5 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 20 Criteria Response at Week 2674.0 percentage of participants
ADA + 10 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 20 Criteria Response at Week 2676.8 percentage of participants
ADA + 20 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 20 Criteria Response at Week 2679.6 percentage of participants
Secondary

Percentage of Participants With American College of Rheumatology (ACR) 50 Criteria Response at Week 26

Response, as defined by ACR 50 criteria at Week 26. A participant is a responder if the following 3 criteria for improvement from Baseline are met: ≥ 50% improvement in tender joint count; ≥ 50% improvement in swollen joint count; and ≥ 50% improvement in at least 3 of the 5 following parameters: * Physician global assessment of disease activity * Patient global assessment of disease activity * Patient assessment of pain * Disability Index of the Health Assessment Questionnaire * Acute phase reactant value (C-reactive protein).

Time frame: Baseline, Week 26

Population: Intent-to-Treat population; participants with a missing response were imputed as non-responders.

ArmMeasureValue (NUMBER)
ADA + 2.5 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 50 Criteria Response at Week 2645.9 percentage of participants
ADA + 5 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 50 Criteria Response at Week 2651.0 percentage of participants
ADA + 10 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 50 Criteria Response at Week 2653.5 percentage of participants
ADA + 20 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 50 Criteria Response at Week 2662.2 percentage of participants
Secondary

Percentage of Participants With American College of Rheumatology (ACR) 70 Criteria Response at Week 26

Response, as defined by ACR 70 criteria at Week 26. A participant is a responder if the following 3 criteria for improvement from Baseline are met: ≥ 70% improvement in tender joint count; ≥ 70% improvement in swollen joint count; and ≥ 70% improvement in at least 3 of the 5 following parameters: * Physician global assessment of disease activity * Patient global assessment of disease activity * Patient assessment of pain * Disability Index of the Health Assessment Questionnaire * Acute phase reactant value (C-reactive protein).

Time frame: Baseline, Week 26

Population: Intent-to-Treat population; participants with a missing response were imputed as non-responders.

ArmMeasureValue (NUMBER)
ADA + 2.5 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 70 Criteria Response at Week 2624.5 percentage of participants
ADA + 5 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 70 Criteria Response at Week 2634.0 percentage of participants
ADA + 10 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 70 Criteria Response at Week 2641.4 percentage of participants
ADA + 20 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 70 Criteria Response at Week 2645.9 percentage of participants
Secondary

Percentage of Participants With American College of Rheumatology (ACR) 90 Criteria Response at Week 26

Response, as defined by ACR 90 criteria at Week 26. A participant is a responder if the following 3 criteria for improvement from Baseline are met: ≥ 90% improvement in tender joint count; ≥ 90% improvement in swollen joint count; and ≥ 90% improvement in at least 3 of the 5 following parameters: * Physician global assessment of disease activity * Patient global assessment of disease activity * Patient assessment of pain * Disability Index of the Health Assessment Questionnaire * Acute phase reactant value (C-reactive protein).

Time frame: Baseline, Week 26

Population: Intent-to-Treat population; participants with a missing response were imputed as non-responders.

ArmMeasureValue (NUMBER)
ADA + 2.5 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 90 Criteria Response at Week 267.1 percentage of participants
ADA + 5 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 90 Criteria Response at Week 2610.0 percentage of participants
ADA + 10 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 90 Criteria Response at Week 2617.2 percentage of participants
ADA + 20 mg MTXPercentage of Participants With American College of Rheumatology (ACR) 90 Criteria Response at Week 2616.3 percentage of participants
Secondary

Percentage of Participants With Clinical Disease Activity Index (CDAI) Remission at Week 26

CDAI is a measure of disease activity derived as follows: CDAI = SJC28 + TJC28 + GH (cm) + PhGA (cm) where TJC28 and SJC28 represent total tender joint count and total swollen joint count, respectively, based on 28 joints (including the left and right side of the body), GH = Patient's Global Assessment of Disease Activity, and PhGA = Physician's Global Assessment of Disease Activity (both measured on a visual analogue scale with a range of 0 \[none\] to 10 \[severe\]). CDAI total score = 0 to 76. CDAI ≤ 2.8 indicates disease remission, \> 2.8 to 10 = low disease activity, \> 10 to 22 = moderate disease activity, and \> 22 = high disease activity.

Time frame: Week 26

Population: Intent-to-Treat population; participants with a missing response were imputed as non-responders.

ArmMeasureValue (NUMBER)
ADA + 2.5 mg MTXPercentage of Participants With Clinical Disease Activity Index (CDAI) Remission at Week 2612.2 percentage of participants
ADA + 5 mg MTXPercentage of Participants With Clinical Disease Activity Index (CDAI) Remission at Week 2622.0 percentage of participants
ADA + 10 mg MTXPercentage of Participants With Clinical Disease Activity Index (CDAI) Remission at Week 2629.3 percentage of participants
ADA + 20 mg MTXPercentage of Participants With Clinical Disease Activity Index (CDAI) Remission at Week 2627.6 percentage of participants
Secondary

Percentage of Participants With DAS28(CRP) Remission at Week 26

Disease remission was defined as a disease activity score, based on CRP, for 28 joints that was \< 2.6 (DAS28\[CRP\] \< 2.6). The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, C-reactive protein, and general health are included in the DAS28 score. Scores on the DAS28 range from 0 to 10.

Time frame: Week 26

Population: Intent-to-Treat population; participants with a missing response were imputed as non-responders.

ArmMeasureValue (NUMBER)
ADA + 2.5 mg MTXPercentage of Participants With DAS28(CRP) Remission at Week 2627.6 percentage of participants
ADA + 5 mg MTXPercentage of Participants With DAS28(CRP) Remission at Week 2632.0 percentage of participants
ADA + 10 mg MTXPercentage of Participants With DAS28(CRP) Remission at Week 2637.4 percentage of participants
ADA + 20 mg MTXPercentage of Participants With DAS28(CRP) Remission at Week 2644.9 percentage of participants
Secondary

Percentage of Participants With No Radiographic Progression at Week 26

No radiographic progression was defined as a change from Baseline in modified Total Sharp Score (mTSS) at Week 26 of ≤ 0.5. mTSS is a measure of change in joint health from digitized images of radiographs of hands and feet. Joints were scored for erosions on a scale of 0 (no damage) to 5 (complete collapse) and joint space narrowing on a scale of 0 (no damage) to 4 (ankylosis or complete dislocation). Erosion scores and narrowing scores were added to obtain the mTSS (range = 0 \[normal\] to 398 \[maximal disease\]). An increase in mTSS from Baseline represents disease progression and/or joint worsening, no change represents halting of disease progression, and a decrease represents improvement.

Time frame: Baseline, Week 26

Population: Intent-to-Treat population; participants with a missing response were imputed as non-responders.

ArmMeasureValue (NUMBER)
ADA + 2.5 mg MTXPercentage of Participants With No Radiographic Progression at Week 2664.3 percentage of participants
ADA + 5 mg MTXPercentage of Participants With No Radiographic Progression at Week 2672.0 percentage of participants
ADA + 10 mg MTXPercentage of Participants With No Radiographic Progression at Week 2676.8 percentage of participants
ADA + 20 mg MTXPercentage of Participants With No Radiographic Progression at Week 2677.6 percentage of participants
Secondary

Percentage of Participants With Simplified Disease Activity Index (SDAI) Remission at Week 26

SDAI is a measure of disease activity derived as follows: SDAI = SJC28 + TJC28 + GH (cm) + PhGA (cm) + CRP (mg/dL), where TJC28 and SJC28 represent total tender joint count and total swollen joint count, respectively, based on 28 joints (including the left and right side of the body), GH = Patient's Global Assessment of Disease Activity, and PhGA = Physician's Global Assessment of Disease Activity (both measured on a visual analogue scale with a range of 0 \[none\] to 10 \[severe\]), and CRP is C-reactive protein measured in mg/dL. SDAI total score = 0 to 86. SDAI ≤ 3.3 indicates disease remission, \> 3.4 to 11 = low disease activity, \> 11 to 26 = moderate disease activity, and \> 26 = high disease activity.

Time frame: Week 26

Population: Intent-to-Treat population; participants with a missing response were imputed as non-responders.

ArmMeasureValue (NUMBER)
ADA + 2.5 mg MTXPercentage of Participants With Simplified Disease Activity Index (SDAI) Remission at Week 2611.2 percentage of participants
ADA + 5 mg MTXPercentage of Participants With Simplified Disease Activity Index (SDAI) Remission at Week 2622.0 percentage of participants
ADA + 10 mg MTXPercentage of Participants With Simplified Disease Activity Index (SDAI) Remission at Week 2628.3 percentage of participants
ADA + 20 mg MTXPercentage of Participants With Simplified Disease Activity Index (SDAI) Remission at Week 2629.6 percentage of participants

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026