| Primary | Percentage of Participants With Any Infusion Reaction | An infusion reaction was defined as any adverse event (AE) that occurred during the infusion or during the 24 hours following the infusion and deemed possibly or probably related to tocilizumab. | Safety Analysis Set (SAS) Population: All randomized participants who received at least one infusion of tocilizumab. | Posted | | Number | | Percentage of Participants | | Baseline (Day 1), and Weeks 4, 8, 12, 16, and 20 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| | Group IDs | Group Description | Statistical Method | Statistical Comment | P-Value | P-Value Comment | Parameter Type | Parameter Value | Dispersion Type | Dispersion Value | Confidence Interval Sides | Confidence Interval % | CI Lower Limit | CI Upper Limit | CI Lower Limit Comment | CI Upper Limit Comment | Estimate Comment | Tested Non-Inferiority | Non-Inferiority Type | Non-Inferiority Comment | Other Analysis Description |
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| | | | | | Risk Difference (RD) | 0.0164 | | | 2-Sided | 95 | -0.2685 | 0.2988 | | | The CI (confidence interval) is calculated by Exact method based on binomial distribution. | No | Superiority or Other | | |
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| Secondary | Percentage of Participants Discontinuing Tocilizumab in Response to an AE or a Serious Adverse Event (SAE) | All occurrences of participants who received at least 1 infusion of tocilizumab and then stopped tocilizumab infusions due to an AE or SAE were analyzed. | | Posted | | Number | | Percentage of Participants | | Baseline (Day 1) and Weeks 4, 8, 12, 16, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | Percentage of Participants Discontinuing Tocilizumab for Other Reasons | Participants that stopped the administration of tocilizumab and discontinued the study prematurely due to reasons other than an AE or SAE were analyzed. | | Posted | | Number | | Percentage of Participants | | Baseline and Weeks, 4, 8, 12, 16, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | Percentage of Participants With Increased Liver Enzyme Values of Greater Than (>)1.5 Times, or >3 Times, or >5 Times Over the Upper Limit of Normal (ULN) by Visit Among Participants Who Completed All Visits | Increased liver enzyme values defined as Alanine Aminotransferase (ALT) and/or Aspartate Aminotransferase (AST) values of >1.5 times, or >3 times, or >5 times over the ULN. Almost none of the participants had increased measurements of AST, thus only values of ALT were presented. None of the participants presented with increased values of ALT above 3 or 5 ULN at any of the visits. ITT Completers is defined as a subset of the participants in the ITT population who completed all study visits. | ITT Completers with liver enzyme datasets for each analyzed visit | Posted | | Number | | Percentage of Participants | | Baseline and Weeks 4, 8, 12, 16, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | Percentage of Participants With Increased Lipid Values by Visit Among Participants Who Completed All Visits | Increased levels of high density lipoproteins (HDL) equal to or greater than (≥)1.5 millimoles per liter (mmol/L), and low density lipoproteins (LDL) ≥4.1 mmol/L, and total cholesterol ≥5.1 mmol/L, are defined according to the Adult Treatment Panel III (ATP-III) guidelines. | | Posted | | Number | | Percentage of Participants | | Screening and Weeks 4, 8, 12, 16, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | Percentage of Participants With a Reduction of at Least 1.2 Points in Disease Activity Score Based on 28-Joint Count (DAS28) by Visit Among Participants Who Completed All Visits | Improvement in Rheumatoid Arthritis (RA) disease activity was measured by the DAS28 score, which is an index combining measurements of swollen and tender joints, acute phase response High sensitivity C-Reactive Protein (hsCRP), and global assessment of disease activity by the participant. A clinically meaningful improvement was defined as a reduction of at least 1.2 units in the DAS28 score during the study period. A low disease activity was defined as a DAS28 score less than (<)3.2, and remission was defined as a DAS28 score <2.6. | | Posted | | Number | | Percentage of Participants | | Weeks 4, 8, 12, 16, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | Percentage of Participants Achieving a DAS28 Score Below 3.2 (Low Disease Activity) by Visit Among Participants Who Completed All Visits | Improvement in RA disease activity was measured by the DAS28 score, which is an index combining measurements of swollen and tender joints, acute phase response hsCRP, and global assessment of disease activity by the participant. A clinically meaningful improvement was defined as a reduction of at least 1.2 units in the DAS28 score during the study period. A low disease activity was defined as a DAS28 score <3.2, and remission was defined as a DAS28 score <2.6. | | Posted | | Number | | Percentage of Participants | | Weeks 4, 8, 12, 16, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | Percentage of Participants Achieving a DAS28 Score Below 2.6 (Remission) by Visit Among Participants Who Completed All Visits | Improvement in RA disease activity was measured by the DAS28 score, which is an index combining measurements of swollen and tender joints, acute phase response hsCRP, and global assessment of disease activity by the participant. A clinically meaningful improvement was defined as a reduction of at least 1.2 units in the DAS28 score during the study period. A low disease activity was defined as a DAS28 score <3.2, and remission was defined as a DAS28 score <2.6. | | Posted | | Number | | Percentage of Participants | | Weeks 4, 8, 12, 16, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | DAS28 Score by Visit Among Participants Who Completed All Visits | Improvement in RA disease activity was measured by the DAS28 score, which is an index combining measurements of swollen and tender joints, acute phase response hsCRP, and global assessment of disease activity by the participant. A clinically meaningful improvement was defined as a reduction of at least 1.2 units in the DAS28 score during the study period. A low disease activity was defined as a DAS28 score <3.2, and remission was defined as a DAS28 score <2.6. | ITT Completers; n = the number of participants analyzed for the given parameter at the specific visit. | Posted | | Mean | Standard Deviation | scores on a scale | | Baseline, Weeks, 4, 8, 12, 16, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | Percentage of Participants Achieving American College of Rheumatology 20 Percent (%) Improvement (ACR20 Response) by Visit Among Participants Who Completed All Visits | ACR20 response is defined as an improvement of ≥20% in swollen joint count (SJC; 66 joints) and tender joint count (TJC; 68 joints) as well as ≥20% improvement in at least 3 of the following 5 remaining ACR assessments: Patient Global Assessment of Pain; Patient Global Assessment of Disease Activity; Physician Global Assessment of Disease Activity; Health Assessment Questionnaire - Disability Index (HAQ-DI); and acute phase reactive factors (Erythrocyte Sedimentation Rate [ESR] or C-Reactive Protein [CRP]). | | Posted | | Number | | Percentage of Participants | | Weeks 4, 8, 12, 16, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | Percentage of Participants Achieving ACR 50% Improvement (ACR50 Response) by Visit Among Participants Who Completed All Visits | ACR50 response is defined as an improvement of ≥50% in SJC (66 joints) and TJC (68 joints) as well as ≥50% improvement in at least 3 of the following 5 remaining ACR assessments: Patient Global Assessment of Pain; Patient Global Assessment of Disease Activity; Physician Global Assessment of Disease Activity; HAQ-DI; and acute phase reactive factors (ESR or CRP). | | Posted | | Number | | Percentage of Participants | | Weeks, 4, 8, 12, 16, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | Percentage of Participants Achieving ACR 70% Improvement (ACR70 Response) by Visit, Among Participants Who Completed All Visits | ACR70 response is defined as an improvement of ≥70% in SJC (66 joints) and TJC (68 joints) as well as ≥70% improvement in at least 3 of the following 5 remaining ACR assessments: Patient Global Assessment of Pain; Patient Global Assessment of Disease Activity; Physician Global Assessment of Disease Activity; HAQ-DI; and acute phase reactive factors (ESR or CRP). | | Posted | | Number | | Percentage of Participants | | Weeks 4, 8, 12, 16, 20 and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | Percentage of Participants Achieving ACR 90% Improvement (ACR90 Response) by Visit Among Participants Who Completed All Visits | ACR90 response is defined as an improvement of ≥90% in SJC (66 joints) and TJC (68 joints) as well as ≥90% improvement in at least 3 of the following 5 remaining ACR assessments: Patient Global Assessment of Pain; Patient Global Assessment of Disease Activity; Physician Global Assessment of Disease Activity; HAQ-DI; and acute phase reactive factors (ESR or CRP). | | Posted | | Number | | Percentage of Participants | | Weeks 4, 8, 12, 16, 20 and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | High Sensitivity C-Reactive Protein (hsCRP) Levels by Visit Among Participants Who Completed All Visits | hsCRP is a marker for inflammation and is measured in milligrams per liter (mg/L). High levels of this protein indicate inflammation in diseases such as RA. | | Posted | | Mean | Standard Deviation | mg/L | | Screening, Baseline, Weeks 4, 8, 12, 16, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | Modified Health Assessment Questionnaire (M-HAQ) Score by Visit Among Participants Who Completed All Visits | M-HAQ is a self-reported, valid assessment of functional disability in RA. Assessment based on ability of participants to perform daily activities in 8 categories: dressing, arising, eating, walking, reaching, gripping, hygiene, and carrying out daily activities. Scores range 0 to 3; without any difficulty=0, with some difficulty=1, with much difficulty=2, unable to do=3. | | Posted | | Mean | Standard Deviation | scores on a scale | | Baseline, Weeks 4, 8, 12, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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| Secondary | Percentage of Participants With Improvement of at Least 0.22 Units in M-HAQ Compared to Baseline Per Visit Among Participants Who Completed All Visits | M-HAQ is a self-reported, valid assessment of functional disability in RA. Assessment based on ability of participants to perform daily activities in 8 categories: dressing, arising, eating, walking, reaching, gripping, hygiene, and carrying out daily activities. Scores range 0 to 3; without any difficulty=0, with some difficulty=1, with much difficulty=2, unable to do=3. | | Posted | | Number | | Percentage of Participants | | Weeks 4, 8. 12, 20, and 24 | | | | ID | Title | Description |
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| OG000 | Tocilizumab, Normal Administration | Participants received tocilizumab 8 mg/kg IV over 60 minutes once every 4 weeks for a total of 6 infusions during the 24-week treatment period. | | OG001 | Tocilizumab, Fast Administration | Participants received tocilizumab 8 mg/kg IV once every 4 weeks for a total of 6 infusions during the 24-week treatment period. The first infusion (Baseline) was given over 60 minutes, and over 31 minutes the following 5 infusions. |
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