Rheumatoid Arthritis
Conditions
Keywords
Musculoskeletal Disease, Arthritis, Joint Disease, Anti-inflammatory agents, Antirheumatic agents, Upadacitinib, ABT-494
Brief summary
The study objective of Period 1 of this study is to compare the safety and efficacy (signs and symptoms) of upadacitinib 30 mg once daily (QD) alone and upadacitinib 15 mg QD alone versus continuing MTX alone adults with moderately to severely active rheumatoid arthritis (RA) with an inadequate response to MTX. The study objective of Period 2 is to evaluate the long term safety, tolerability, and efficacy of upadacitinib 30 mg QD and 15 mg QD in adults with RA who had completed Period 1.
Detailed description
The study includes a 35-day screening period; a 14-week randomized, double-blind, parallel-group, controlled treatment period (Period 1); a 246-week blinded extension period (Period 2); and a 30-day follow-up visit. Participants who met eligibility criteria were to be randomized in a 2:2:1:1 ratio to one of four treatment groups: * Group 1: upadacitinib 30 mg QD (Period 1) → upadacitinib 30 mg QD (Period 2) * Group 2: upadacitinib 15 mg QD (Period 1) → upadacitinib 15 mg QD (Period 2) * Group 3: MTX (Period 1) → upadacitinib 30 mg QD (Period 2) * Group 4: MTX (Period 1) → upadacitinib 15 mg QD (Period 2) Starting with implementation of Protocol Amendment 5, all participants in the extension period will receive open-label upadacitinib 15 mg QD, including those currently on upadacitinib 30 mg QD.
Interventions
Capsule; Oral
Tablet; Oral
Tablet; Oral
Capsule; Oral
Sponsors
Study design
Eligibility
Inclusion criteria
* Diagnosis of RA for \>= 3 months. * Subjects must have been on oral or parenteral MTX therapy \>= 3 months and on a stable dose for \>= 4 weeks prior to first dose of study drug. * Must have discontinued all conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs) (other than MTX) \>= 4 weeks prior to first dose of study drug. * Meets the following minimum disease activity criteria: \>= 6 swollen joints (based on 66 joint counts) and \>= 6 tender joints (based on 68 joint counts) at Screening and Baseline Visits.
Exclusion criteria
* Prior exposure to any Janus kinase (JAK) inhibitor (including but not limited to tofacitinib, baricitinib, and filgotinib). * Prior exposure to any biological disease-modifying anti-rheumatic drugs (bDMARDs). * Current diagnosis of inflammatory joint disease other than RA. Current diagnosis of secondary Sjogren's Syndrome is permitted.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 14 | Baseline and week 14 | The primary endpoint for United States (US)/Food and Drug Administration (FDA) regulatory purposes was ACR 20% response (ACR20) at Week 14. Participants who met the following 3 conditions for improvement from baseline were classified as meeting the ACR20 response criteria: 1. ≥ 20% improvement in 68-tender joint count; 2. ≥ 20% improvement in 66-swollen joint count; and 3. ≥ 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 * Health Assessment Questionnaire - Disability Index (HAQ-DI) * High-sensitivity C-reactive protein (hsCRP). |
| Percentage of Participants Achieving Low Disease Activity (LDA) Based on DAS28(CRP) at Week 14 | Week 14 | The primary endpoint for European Union (EU)/European Medicines Agency (EMA) regulatory purposes was low disease activity, based on a Disease Activity Score 28 (DAS28)-CRP score of ≤ 3.2 at Week 14. The DAS28 is a composite index used to assess rheumatoid arthritis disease activity, calculated based on the tender joint count (out of 28 evaluated joints), swollen joint count (out of 28 evaluated joints), Patient's Global Assessment of Disease Activity (0-100 mm), and hsCRP (in mg/L). Scores on the DAS28 range from 0 to approximately 10, where higher scores indicate more disease activity. A DAS28 score less than or equal to 3.2 indicates low disease activity. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change From Baseline in Short-Form 36 (SF-36) Physical Component Score (PCS) at Week 14 | Baseline to week 14 | The Short Form 36-Item Health Survey (SF-36) Version 2 is a self-administered questionnaire that measures the impact of disease on overall quality of life during the past 4 weeks. The SF-36 consists of 36 questions in eight domains (physical function, pain, general and mental health, vitality, social function, physical and emotional health). The physical component score is a weighted combination of the 8 subscales with positive weighting for physical functioning, role-physical, bodily pain, and general health. The PCS was calculated using norm-based scoring so that 50 is the average score and the standard deviation equals 10. Higher scores are associated with better functioning/quality of life; a positive change from baseline score indicates an improvement. |
| Percentage of Participants Achieving Clinical Remission (CR) Based on DAS28(CRP) at Week 14 | Week 14 | The DAS28 is a composite index used to assess rheumatoid arthritis disease activity, calculated based on the tender joint count (out of 28 evaluated joints), swollen joint count (out of 28 evaluated joints), Patient's Global Assessment of Disease Activity (0-100 mm), and hsCRP (in mg/L). Scores on the DAS28 range from 0 to approximately 10, where higher scores indicate more disease activity. A DAS28 score less than 2.6 indicates clinical remission. |
| Change From Baseline in in Disease Activity Score 28 (CRP) at Week 14 | Baseline to week 14 | The DAS28 is a composite index used to assess rheumatoid arthritis disease activity, calculated based on the tender joint count (out of 28 evaluated joints), swollen joint count (out of 28 evaluated joints), Patient's Global Assessment of Disease Activity (0-100 mm), and hsCRP (in mg/L). Scores on the DAS28 range from 0 to approximately 10, where higher scores indicate more disease activity. A negative change from baseline in DAS28 (CRP) indicates improvement in disease activity. |
| Percentage of Participants With an American College of Rheumatology 50% (ACR50) Response at Week 14 | Baseline and week 14 | Participants who met the following 3 conditions for improvement from baseline were classified as meeting the ACR50 response criteria: 1. ≥ 50% improvement in 68-tender joint count; 2. ≥ 50% improvement in 66-swollen joint count; and 3. ≥ 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 * Health Assessment Questionnaire - Disability Index (HAQ-DI) * High-sensitivity C-reactive protein (hsCRP). |
| Percentage of Participants With an American College of Rheumatology 70% (ACR70) Response at Week 14 | Baseline and week 14 | Participants who met the following 3 conditions for improvement from baseline were classified as meeting the ACR50 response criteria: 1. ≥ 70% improvement in 68-tender joint count; 2. ≥ 70% improvement in 66-swollen joint count; and 3. ≥ 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 * Health Assessment Questionnaire - Disability Index (HAQ-DI) * High-sensitivity C-reactive protein (hsCRP). |
| Change From Baseline in Duration of Morning Stiffness at Week 14 | Baseline to week 14 | Participants were asked to indicate the time it took for them to get as limber as possible after awakening with morning stiffness over the past 7 days. A negative change from Baseline indicates improvement. |
| Change From Baseline in Heath Assessment Questionnaire and Disability Index (HAQ-DI) at Week 14 | Baseline to week 14 | The Health Assessment Questionnaire - Disability Index is a patient-reported questionnaire that measures the degree of difficulty a person has in accomplishing tasks in 8 functional areas (dressing, arising, eating, walking, hygiene, reaching, gripping, and errands and chores) over the past week. Participants assessed their ability to do each task on a scale from 0 (without any difficulty) to 3 (unable to do). Scores were averaged to provide an overall score ranging from 0 to 3, where 0 represents no disability and 3 represents very severe, high-dependency disability. A negative change from Baseline in the overall score indicates improvement. |
Countries
Argentina, Australia, Austria, Belgium, Bulgaria, Chile, Czechia, Estonia, Greece, Hungary, Israel, Italy, Japan, Mexico, Poland, Portugal, Puerto Rico, Romania, Russia, Serbia, South Africa, Spain, Turkey (Türkiye), Ukraine, United States
Participant flow
Recruitment details
A total of 648 participants with rheumatoid arthritis (RA) on a stable dose of methotrexate (MTX) were randomized at 138 study sites located in 24 countries.
Pre-assignment details
Participants were randomized in a 2:2:1:1 ratio to 1 of 4 groups: * Upadacitinib 30 mg (Periods 1 and 2) * Upadacitinib 15 mg (Periods 1 and 2) * MTX (Period 1) → upadacitinib 30 mg (Period 2) * MTX (Period 1) → upadacitinib 15 mg (Period 2) Randomization was stratified by geographic region. The MTX groups were pooled for Week 14 analyses. Starting with Amend. 5 & during Period 2, all participants received open-label upadacitinib 15 mg, including participants receiving upadacitinib 30 mg
Participants by arm
| Arm | Count |
|---|---|
| Methotrexate Participants randomized to receive up to 25 mg methotrexate once a week and placebo to upadacitinib once daily for 14 weeks in Period 1. | 216 |
| Upadacitinib 15 mg Participants randomized to receive upadacitinib 15 mg once daily and placebo to methotrexate once a week for 14 weeks in Period 1. | 217 |
| Upadacitinib 30 mg Participants randomized to receive upadacitinib 30 mg once daily and placebo to methotrexate once a week for 14 weeks in Period 1. | 215 |
| Total | 648 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 | FG003 | FG004 |
|---|---|---|---|---|---|---|
| Period 1 | Adverse Event | 1 | 5 | 3 | 0 | 0 |
| Period 1 | Lost to Follow-up | 0 | 4 | 1 | 0 | 0 |
| Period 1 | Other | 2 | 1 | 0 | 0 | 0 |
| Period 1 | Withdrawal by Subject | 10 | 6 | 6 | 0 | 0 |
| Period 2 | Adverse Event | 0 | 0 | 0 | 25 | 34 |
| Period 2 | COVID-19 Related | 0 | 0 | 0 | 1 | 2 |
| Period 2 | Lost to Follow-up | 0 | 0 | 0 | 17 | 9 |
| Period 2 | Other | 0 | 0 | 0 | 37 | 31 |
| Period 2 | Withdrawal by Subject | 0 | 0 | 0 | 38 | 44 |
Baseline characteristics
| Characteristic | Upadacitinib 15 mg | Upadacitinib 30 mg | Methotrexate | Total |
|---|---|---|---|---|
| Age, Continuous | 54.5 years STANDARD_DEVIATION 12.2 | 53.1 years STANDARD_DEVIATION 12.72 | 55.3 years STANDARD_DEVIATION 11.12 | 54.3 years STANDARD_DEVIATION 12.05 |
| Age, Customized 40 - 64 years | 147 Participants | 141 Participants | 148 Participants | 436 Participants |
| Age, Customized < 40 years | 28 Participants | 31 Participants | 23 Participants | 82 Participants |
| Age, Customized ≥ 65 years | 42 Participants | 43 Participants | 45 Participants | 130 Participants |
| Disease Activity Score 28 Based on CRP (DAS28[CRP]) | 5.6 units on a scale STANDARD_DEVIATION 0.92 | 5.6 units on a scale STANDARD_DEVIATION 1.06 | 5.6 units on a scale STANDARD_DEVIATION 1.04 | 5.6 units on a scale STANDARD_DEVIATION 1.01 |
| Duration of RA Diagnosis | 7.5 years STANDARD_DEVIATION 8.88 | 6.5 years STANDARD_DEVIATION 6.98 | 5.8 years STANDARD_DEVIATION 6.63 | 6.6 years STANDARD_DEVIATION 7.58 |
| Ethnicity (NIH/OMB) Hispanic or Latino | 52 Participants | 54 Participants | 50 Participants | 156 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 165 Participants | 161 Participants | 166 Participants | 492 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Geographic Region Asia - Japan | 22 Participants | 21 Participants | 22 Participants | 65 Participants |
| Geographic Region Eastern Europe | 80 Participants | 80 Participants | 79 Participants | 239 Participants |
| Geographic Region North America | 64 Participants | 64 Participants | 64 Participants | 192 Participants |
| Geographic Region Other | 13 Participants | 12 Participants | 12 Participants | 37 Participants |
| Geographic Region South/Central America | 30 Participants | 30 Participants | 31 Participants | 91 Participants |
| Geographic Region Western Europe | 8 Participants | 8 Participants | 8 Participants | 24 Participants |
| Health Assessment Questionnaire - Disability Index (HAQ-DI) | 1.5 units on a scale STANDARD_DEVIATION 0.66 | 1.5 units on a scale STANDARD_DEVIATION 0.65 | 1.5 units on a scale STANDARD_DEVIATION 0.66 | 1.5 units on a scale STANDARD_DEVIATION 0.66 |
| High-sensitivity C-reactive Protein (hsCRP) | 14.0 mg/L STANDARD_DEVIATION 16.49 | 16.3 mg/L STANDARD_DEVIATION 20.77 | 14.5 mg/L STANDARD_DEVIATION 17.33 | 14.9 mg/L STANDARD_DEVIATION 18.28 |
| Patient's Assessment of Pain | 62.3 mm STANDARD_DEVIATION 22.53 | 61.9 mm STANDARD_DEVIATION 22.12 | 62.5 mm STANDARD_DEVIATION 21.26 | 62.3 mm STANDARD_DEVIATION 21.94 |
| Patient's Global Assessment of Disease Activity | 62.2 mm STANDARD_DEVIATION 22.29 | 59.4 mm STANDARD_DEVIATION 22.79 | 59.6 mm STANDARD_DEVIATION 21.78 | 60.4 mm STANDARD_DEVIATION 22.29 |
| Physician's Global Assessment of Disease Activity | 65.7 mm STANDARD_DEVIATION 18.49 | 62.6 mm STANDARD_DEVIATION 17.81 | 62.1 mm STANDARD_DEVIATION 17.47 | 63.5 mm STANDARD_DEVIATION 17.98 |
| Race/Ethnicity, Customized American Indian/Alaska Native | 4 Participants | 3 Participants | 3 Participants | 10 Participants |
| Race/Ethnicity, Customized Asian | 24 Participants | 21 Participants | 24 Participants | 69 Participants |
| Race/Ethnicity, Customized Black or African American | 15 Participants | 9 Participants | 11 Participants | 35 Participants |
| Race/Ethnicity, Customized Multiple | 1 Participants | 2 Participants | 2 Participants | 5 Participants |
| Race/Ethnicity, Customized White | 173 Participants | 180 Participants | 176 Participants | 529 Participants |
| Sex: Female, Male Female | 174 Participants | 170 Participants | 179 Participants | 523 Participants |
| Sex: Female, Male Male | 43 Participants | 45 Participants | 37 Participants | 125 Participants |
| Swollen Joint Count | 16.4 joints STANDARD_DEVIATION 10.94 | 16.9 joints STANDARD_DEVIATION 10.23 | 16.9 joints STANDARD_DEVIATION 11.52 | 16.7 joints STANDARD_DEVIATION 10.9 |
| Tender Joint Count | 24.5 joints STANDARD_DEVIATION 15.1 | 24.8 joints STANDARD_DEVIATION 15.19 | 25.2 joints STANDARD_DEVIATION 15.99 | 24.8 joints STANDARD_DEVIATION 15.41 |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk | EG004 affected / at risk | EG005 affected / at risk |
|---|---|---|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 216 | 0 / 217 | 0 / 215 | 7 / 318 | 5 / 311 | 4 / 205 |
| other Total, other adverse events | 49 / 216 | 43 / 217 | 51 / 215 | 219 / 318 | 211 / 311 | 82 / 205 |
| serious Total, serious adverse events | 7 / 216 | 11 / 217 | 6 / 215 | 95 / 318 | 75 / 311 | 22 / 205 |
Outcome results
Percentage of Participants Achieving Low Disease Activity (LDA) Based on DAS28(CRP) at Week 14
The primary endpoint for European Union (EU)/European Medicines Agency (EMA) regulatory purposes was low disease activity, based on a Disease Activity Score 28 (DAS28)-CRP score of ≤ 3.2 at Week 14. The DAS28 is a composite index used to assess rheumatoid arthritis disease activity, calculated based on the tender joint count (out of 28 evaluated joints), swollen joint count (out of 28 evaluated joints), Patient's Global Assessment of Disease Activity (0-100 mm), and hsCRP (in mg/L). Scores on the DAS28 range from 0 to approximately 10, where higher scores indicate more disease activity. A DAS28 score less than or equal to 3.2 indicates low disease activity.
Time frame: Week 14
Population: Full analysis set; participants who prematurely discontinued from study drug prior to Week 14 or for whom DAS28 data were missing at Week 14 were considered non-responders.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Methotrexate | Percentage of Participants Achieving Low Disease Activity (LDA) Based on DAS28(CRP) at Week 14 | 19.4 percentage of participants |
| Upadacitinib 15 mg | Percentage of Participants Achieving Low Disease Activity (LDA) Based on DAS28(CRP) at Week 14 | 44.7 percentage of participants |
| Upadacitinib 30 mg | Percentage of Participants Achieving Low Disease Activity (LDA) Based on DAS28(CRP) at Week 14 | 53.0 percentage of participants |
Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 14
The primary endpoint for United States (US)/Food and Drug Administration (FDA) regulatory purposes was ACR 20% response (ACR20) at Week 14. Participants who met the following 3 conditions for improvement from baseline were classified as meeting the ACR20 response criteria: 1. ≥ 20% improvement in 68-tender joint count; 2. ≥ 20% improvement in 66-swollen joint count; and 3. ≥ 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 * Health Assessment Questionnaire - Disability Index (HAQ-DI) * High-sensitivity C-reactive protein (hsCRP).
Time frame: Baseline and week 14
Population: Full analysis set; participants who prematurely discontinued from study drug prior to Week 14 or for whom ACR data were missing at Week 14 were considered non-responders.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Methotrexate | Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 14 | 41.2 percentage of participants |
| Upadacitinib 15 mg | Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 14 | 67.7 percentage of participants |
| Upadacitinib 30 mg | Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 14 | 71.2 percentage of participants |
Change From Baseline in Duration of Morning Stiffness at Week 14
Participants were asked to indicate the time it took for them to get as limber as possible after awakening with morning stiffness over the past 7 days. A negative change from Baseline indicates improvement.
Time frame: Baseline to week 14
Population: Full analysis set participants with available data; a mixed effect model repeat measurement (MMRM) analysis with data from observed cases to Week 14 was used.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) |
|---|---|---|
| Methotrexate | Change From Baseline in Duration of Morning Stiffness at Week 14 | -53.03 minutes |
| Upadacitinib 15 mg | Change From Baseline in Duration of Morning Stiffness at Week 14 | -94.56 minutes |
| Upadacitinib 30 mg | Change From Baseline in Duration of Morning Stiffness at Week 14 | -102.34 minutes |
Change From Baseline in Heath Assessment Questionnaire and Disability Index (HAQ-DI) at Week 14
The Health Assessment Questionnaire - Disability Index is a patient-reported questionnaire that measures the degree of difficulty a person has in accomplishing tasks in 8 functional areas (dressing, arising, eating, walking, hygiene, reaching, gripping, and errands and chores) over the past week. Participants assessed their ability to do each task on a scale from 0 (without any difficulty) to 3 (unable to do). Scores were averaged to provide an overall score ranging from 0 to 3, where 0 represents no disability and 3 represents very severe, high-dependency disability. A negative change from Baseline in the overall score indicates improvement.
Time frame: Baseline to week 14
Population: Full analysis set participants with available data at baseline; multiple imputation was used for missing data.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) |
|---|---|---|
| Methotrexate | Change From Baseline in Heath Assessment Questionnaire and Disability Index (HAQ-DI) at Week 14 | -0.32 scores on a scale |
| Upadacitinib 15 mg | Change From Baseline in Heath Assessment Questionnaire and Disability Index (HAQ-DI) at Week 14 | -0.65 scores on a scale |
| Upadacitinib 30 mg | Change From Baseline in Heath Assessment Questionnaire and Disability Index (HAQ-DI) at Week 14 | -0.73 scores on a scale |
Change From Baseline in in Disease Activity Score 28 (CRP) at Week 14
The DAS28 is a composite index used to assess rheumatoid arthritis disease activity, calculated based on the tender joint count (out of 28 evaluated joints), swollen joint count (out of 28 evaluated joints), Patient's Global Assessment of Disease Activity (0-100 mm), and hsCRP (in mg/L). Scores on the DAS28 range from 0 to approximately 10, where higher scores indicate more disease activity. A negative change from baseline in DAS28 (CRP) indicates improvement in disease activity.
Time frame: Baseline to week 14
Population: Full analysis set participants with available data at baseline; multiple imputation was used for missing post-baseline data.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) |
|---|---|---|
| Methotrexate | Change From Baseline in in Disease Activity Score 28 (CRP) at Week 14 | -1.20 scores on a scale |
| Upadacitinib 15 mg | Change From Baseline in in Disease Activity Score 28 (CRP) at Week 14 | -2.29 scores on a scale |
| Upadacitinib 30 mg | Change From Baseline in in Disease Activity Score 28 (CRP) at Week 14 | -2.61 scores on a scale |
Change From Baseline in Short-Form 36 (SF-36) Physical Component Score (PCS) at Week 14
The Short Form 36-Item Health Survey (SF-36) Version 2 is a self-administered questionnaire that measures the impact of disease on overall quality of life during the past 4 weeks. The SF-36 consists of 36 questions in eight domains (physical function, pain, general and mental health, vitality, social function, physical and emotional health). The physical component score is a weighted combination of the 8 subscales with positive weighting for physical functioning, role-physical, bodily pain, and general health. The PCS was calculated using norm-based scoring so that 50 is the average score and the standard deviation equals 10. Higher scores are associated with better functioning/quality of life; a positive change from baseline score indicates an improvement.
Time frame: Baseline to week 14
Population: Full analysis set participants with available data; a mixed effect model repeat measurement (MMRM) analysis with data from observed cases to Week 14 was used.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) |
|---|---|---|
| Methotrexate | Change From Baseline in Short-Form 36 (SF-36) Physical Component Score (PCS) at Week 14 | 4.32 scores on a scale |
| Upadacitinib 15 mg | Change From Baseline in Short-Form 36 (SF-36) Physical Component Score (PCS) at Week 14 | 8.28 scores on a scale |
| Upadacitinib 30 mg | Change From Baseline in Short-Form 36 (SF-36) Physical Component Score (PCS) at Week 14 | 10.19 scores on a scale |
Percentage of Participants Achieving Clinical Remission (CR) Based on DAS28(CRP) at Week 14
The DAS28 is a composite index used to assess rheumatoid arthritis disease activity, calculated based on the tender joint count (out of 28 evaluated joints), swollen joint count (out of 28 evaluated joints), Patient's Global Assessment of Disease Activity (0-100 mm), and hsCRP (in mg/L). Scores on the DAS28 range from 0 to approximately 10, where higher scores indicate more disease activity. A DAS28 score less than 2.6 indicates clinical remission.
Time frame: Week 14
Population: Full analysis set; participants who prematurely discontinued from study drug prior to Week 14 or for whom DAS28 data were missing at Week 14 were considered non-responders
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Methotrexate | Percentage of Participants Achieving Clinical Remission (CR) Based on DAS28(CRP) at Week 14 | 8.3 percentage of participants |
| Upadacitinib 15 mg | Percentage of Participants Achieving Clinical Remission (CR) Based on DAS28(CRP) at Week 14 | 28.1 percentage of participants |
| Upadacitinib 30 mg | Percentage of Participants Achieving Clinical Remission (CR) Based on DAS28(CRP) at Week 14 | 40.5 percentage of participants |
Percentage of Participants With an American College of Rheumatology 50% (ACR50) Response at Week 14
Participants who met the following 3 conditions for improvement from baseline were classified as meeting the ACR50 response criteria: 1. ≥ 50% improvement in 68-tender joint count; 2. ≥ 50% improvement in 66-swollen joint count; and 3. ≥ 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 * Health Assessment Questionnaire - Disability Index (HAQ-DI) * High-sensitivity C-reactive protein (hsCRP).
Time frame: Baseline and week 14
Population: Full analysis set; participants who prematurely discontinued from study drug prior to Week 14 or for whom ACR data were missing at Week 14 were considered non-responders.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Methotrexate | Percentage of Participants With an American College of Rheumatology 50% (ACR50) Response at Week 14 | 15.3 percentage of participants |
| Upadacitinib 15 mg | Percentage of Participants With an American College of Rheumatology 50% (ACR50) Response at Week 14 | 41.9 percentage of participants |
| Upadacitinib 30 mg | Percentage of Participants With an American College of Rheumatology 50% (ACR50) Response at Week 14 | 52.1 percentage of participants |
Percentage of Participants With an American College of Rheumatology 70% (ACR70) Response at Week 14
Participants who met the following 3 conditions for improvement from baseline were classified as meeting the ACR50 response criteria: 1. ≥ 70% improvement in 68-tender joint count; 2. ≥ 70% improvement in 66-swollen joint count; and 3. ≥ 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 * Health Assessment Questionnaire - Disability Index (HAQ-DI) * High-sensitivity C-reactive protein (hsCRP).
Time frame: Baseline and week 14
Population: Full analysis set; participants who prematurely discontinued from study drug prior to Week 14 or for whom ACR data were missing at Week 14 were considered non-responders.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Methotrexate | Percentage of Participants With an American College of Rheumatology 70% (ACR70) Response at Week 14 | 2.8 percentage of participants |
| Upadacitinib 15 mg | Percentage of Participants With an American College of Rheumatology 70% (ACR70) Response at Week 14 | 22.6 percentage of participants |
| Upadacitinib 30 mg | Percentage of Participants With an American College of Rheumatology 70% (ACR70) Response at Week 14 | 33.0 percentage of participants |