| Primary | Percentage of Participants Who Were Week 8 Responders With Durable Clinical Response at Week 56 | Durable clinical response was defined as reduction in complete Full Mayo score of ≥3 points and ≥30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥1 point or absolute rectal bleeding subscore of ≤1 point at both Week 8 and 56. Clinical response was defined as reduction in complete full Mayo score of ≥3 points and ≥30% from Baseline (Week 0) with decrease in rectal bleeding subscore of ≥1 point or absolute rectal bleeding subscore of ≤1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and physician's global assessment [PGA]), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | ITT set: all participants that were intended to be treated with adalimumab. At Week 8, all participants who had received adalimumab treatment at least once were included and at Week 56, all participants who had clinical response at Week 8 were included. A participant was a Week 8 responder if they had a clinical response at Week 8. | Posted | | Number | 95% Confidence Interval | percentage of participants | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| | | Title | Denominators | Categories |
|---|
| | | Title | Measurements |
|---|
| - OG00053.95(42.13 to 65.45)
|
|
| |
| Primary | Percentage of Participants With Clinical Response at Week 8 | Clinical response was defined as reduction in complete full Mayo score of ≥3 points and ≥30% from Baseline (Week 0) with decrease in rectal bleeding subscore of ≥1 point or absolute rectal bleeding subscore of ≤1 point at week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | ITT set: all participants that were intended to be treated with adalimumab. At Week 8, all participants who had received adalimumab treatment at least once were included and at Week 56, all participants who had clinical response at Week 8 were included. | Posted | | Number | 95% Confidence Interval | percentage of participants | | Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Primary | Percentage of Participants With Clinical Response at Week 24 | Clinical response was defined as reduction in complete full Mayo score of ≥3 points and ≥30% from Baseline (Week 0) with decrease in rectal bleeding subscore of ≥1 point or absolute rectal bleeding subscore of ≤1 point at Week 24. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | | Posted | | Number | 95% Confidence Interval | percentage of participants | | Week 24 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Primary | Percentage of Participants With Clinical Response at Week 56 | Clinical response was defined as reduction in complete full Mayo score of ≥3 points and ≥30% from Baseline (Week 0) with decrease in rectal bleeding subscore of ≥1 point or absolute rectal bleeding subscore of ≤1 point at Week 56. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | | Posted | | Number | 95% Confidence Interval | percentage of participants | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Percentage of Participants With Clinical Remission at Week 8 | Clinical remission was defined as the full Mayo score ≤2 points, with no individual sub-score exceeding 1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | | Posted | | Number | | percentage of participants | | Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
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| Secondary | Percentage of Participants With Clinical Remission at Week 56 | Clinical remission was defined as the full Mayo score ≤2 points, with no individual sub-score exceeding 1 point at Week 56. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | | Posted | | Number | | percentage of participants | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Percentage of Participants Who Were Week 8 Responders With Clinical Remission at Week 8 | Clinical remission was defined as the full Mayo score ≤2 points, with no individual sub-score exceeding 1 point at Week 8. Clinical response was defined as reduction in complete full Mayo score of ≥ 3 points and ≥ 30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥ 1 point or absolute rectal bleeding subscore of ≤ 1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | ITT set. A participant was a Week 8 responder if they had a clinical response at Week 8. | Posted | | Number | | percentage of participants | | Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Percentage of Participants Who Were Week 8 Responders With Clinical Remission at Week 56 | Clinical remission was defined as the full Mayo score ≤2 points, with no individual sub-score exceeding 1 point at Week 56. Clinical response was defined as reduction in complete full Mayo score of ≥ 3 points and ≥ 30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥ 1 point or absolute rectal bleeding subscore of ≤ 1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | ITT set. A participant was a Week 8 responder if they had a clinical response at Week 8. | Posted | | Number | | percentage of participants | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Percentage of Participants With Steroid-free Remission at Week 8 | Steroid free remission was defined as participants who were in remission without the use of systemic steroids from Visit 1 (Baseline) prior to assessment. | | Posted | | Number | | percentage of participants | | Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| | |
| Secondary | Percentage of Participants With Steroid-free Remission at Week 56 | Steroid free remission was defined as participants who were in remission without the use of systemic steroids within the past 12 weeks prior to assessment. | | Posted | | Number | | percentage of participants | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| | |
| Secondary | Percentage of Participants Who Were Week 8 Responders With Steroid-free Remission at Week 8 | Steroid-free remission was defined as participants who were in remission without the use of systemic steroids within the past 12 weeks prior to assessment. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. Clinical response was defined as reduction in complete full Mayo score of ≥ 3 points and ≥ 30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥ 1 point or absolute rectal bleeding subscore of ≤ 1 point at Week 8. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | ITT set. A participant was a Week 8 responder if they had a clinical response at Week 8. | Posted | | Number | | percentage of participants | | Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Percentage of Participants Who Were Week 8 Responders With Steroid-free Remission at Week 56 | Steroid free remission was defined as participants who were in remission without the use of systemic steroids within the past 12 weeks prior to assessment. Clinical response was defined as reduction in complete full Mayo score of ≥ 3 points and ≥ 30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥ 1 point or absolute rectal bleeding subscore of ≤ 1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | ITT set. A participant was a Week 8 responder if they had a clinical response at Week 8. | Posted | | Number | | percentage of participants | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Percentage of Participants With Steroid-free Response at Week 8 | Steroid-free response was defined as participants who were in clinical response without the use of systemic steroids within the past 8 weeks prior to assessment. Clinical response was defined as reduction in complete full Mayo score of ≥ 3 points and ≥ 30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥ 1 point or absolute rectal bleeding subscore of ≤ 1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | | Posted | | Number | | percentage of participants | | Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Percentage of Participants With Steroid-free Response at Week 56 | Steroid-free response was defined as participants who were in clinical response without the use of systemic steroids within the past 8 weeks prior to assessment. Clinical response was defined as reduction in complete full Mayo score of ≥ 3 points and ≥ 30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥ 1 point or absolute rectal bleeding subscore of ≤ 1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | | Posted | | Number | | percentage of participants | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Percentage of Participants Who Were Week 8 Responders With Steroid-free Response at Week 8 | Steroid free response was defined as participants who were in clinical response without the use of systemic steroids within the past 8 weeks prior to assessment (in Week 8 clinical responders).Clinical response was defined as reduction in complete full Mayo score of ≥ 3 points and ≥ 30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥ 1 point or absolute rectal bleeding subscore of ≤ 1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | ITT set. A participant was a Week 8 responder if they had a clinical response at Week 8. | Posted | | Number | | percentage of participants | | Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
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| Secondary | Percentage of Participants Who Were Week 8 Responders With Steroid-free Response at Week 56 | Steroid free response was defined as participants who were in clinical response without the use of systemic steroids within the past 12 weeks prior to assessment (in Week 8 clinical responders). A participant was a Week 8 responder if they had a clinical response at Week 8. Clinical response was defined as reduction in complete full Mayo score of ≥ 3 points and ≥ 30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥ 1 point or absolute rectal bleeding subscore of ≤ 1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | ITT set. A participant was a Week 8 responder if they had a clinical response at Week 8. | Posted | | Number | | percentage of participants | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Percentage of Participants With Mucosal Healing at Week 8 | Mucosal healing was defined as an endoscopy sub-score of 0 or 1 at week 8. Endoscopic findings were scored on a scale from 0 to 3 as follows: 0 = Normal or inactive disease; 1 = Mild disease (erythema, decreased vascular pattern, mild friability); 2 = Moderate disease (marked erythema, lack of vascular pattern, friability, erosions); 3 = Severe disease (spontaneous bleeding, ulceration). The higher the score, the more severe the disease. | | Posted | | Number | | percentage of participants | | Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Percentage of Participants With Mucosal Healing at Week 56 | Mucosal healing was defined as an endoscopy sub-score of 0 or 1 at Week 56. Endoscopic findings were scored on a scale from 0 to 3 as follows: 0 = Normal or inactive disease; 1 = Mild disease (erythema, decreased vascular pattern, mild friability); 2 = Moderate disease (marked erythema, lack of vascular pattern, friability, erosions); 3 = Severe disease (spontaneous bleeding, ulceration). The higher the score, the more severe the disease. | | Posted | | Number | | percentage of participants | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Percentage of Participants Who Were Week 8 Responders With Mucosal Healing at Week 8 | Mucosal healing was defined as an endoscopy sub-score of 0 or 1 at Week 8. Endoscopic findings were scored on a scale from 0 to 3 (higher score, worse disease): 0=Normal or inactive disease; 1=Mild disease (erythema, decreased vascular pattern, mild friability); 2=Moderate disease (marked erythema, lack of vascular pattern, friability, erosions); 3=Severe disease (spontaneous bleeding, ulceration). Clinical response was defined as reduction in complete full Mayo score of ≥ 3 points and ≥ 30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥ 1 point or absolute rectal bleeding subscore of ≤ 1 point at Week 8. Mayo score measures disease activity for ulcerative colitis from 0 (normal or inactive disease) to 12 (severe disease), calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each ranging from 0 (normal) to 3 (severe disease). Negative change in Mayo score indicates improvement. | ITT set. A participant was a Week 8 responder if they had a clinical response at Week 8. | Posted | | Number | | percentage of participants | | Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
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| Secondary | Percentage of Participants Who Were Week 8 Responders With Mucosal Healing at Week 56 | Mucosal healing was defined as an endoscopy sub-score of 0 or 1 at Week 56. Endoscopic findings were scored on a scale from 0 to 3 (higher score, worse disease): 0=Normal or inactive disease; 1=Mild disease (erythema, decreased vascular pattern, mild friability); 2=Moderate disease (marked erythema, lack of vascular pattern, friability, erosions); 3=Severe disease (spontaneous bleeding, ulceration). Clinical response was defined as reduction in complete full Mayo score of ≥ 3 points and ≥ 30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥ 1 point or absolute rectal bleeding subscore of ≤ 1 point at Week 8. Mayo score measures disease activity for ulcerative colitis from 0 (normal or inactive disease) to 12 (severe disease), calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each ranging from 0 (normal) to 3 (severe disease). Negative change in Mayo score indicates improvement. | ITT set. A participant was a Week 8 responder if they had a clinical response at Week 8. | Posted | | Number | | percentage of participants | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Change in Partial Mayo Score From Baseline to Week 8 in Participants Who Were Clinical Responders at Week 56 | The partial Mayo score is based on the Mayo score, which is a tool designed to measure disease activity for ulcerative colitis. The partial Mayo score (Mayo score without endoscopy) ranges from 0 (normal or inactive disease) to 9 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in partial Mayo score indicates improvement. | ITT set of participants who were clinical responders at Week 56 | Posted | | Mean | Standard Deviation | score on a scale | | Baseline, Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
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| Secondary | Change in Full Mayo Score From Baseline to Week 8 in Participants Who Were Clinical Responders at Week 56 | Clinical response was defined as reduction in complete full Mayo score of ≥ 3 points and ≥ 30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥ 1 point or absolute rectal bleeding subscore of ≤ 1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and physician's global assessment [PGA]), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | ITT set of participants who were clinical responders at Week 56 with evaluable data for this Outcome Measure. | Posted | | Mean | Standard Deviation | score on a scale | | Baseline, Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Change in Full Mayo Score From Baseline to Week 56 in Participants Who Were Clinical Responders at Week 56 | Clinical response was defined as reduction in complete full Mayo score of ≥ 3 points and ≥ 30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥ 1 point or absolute rectal bleeding subscore of ≤ 1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and physician's global assessment [PGA]), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | ITT set of participants who were clinical responders at Week 56 | Posted | | Mean | Standard Deviation | score on a scale | | Baseline, Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Fecal Calprotectin Level at Week 8 | Fecal calprotectin is an indicator of inflammation in the colon with higher levels indicative of higher levels of inflammation. | | Posted | | Mean | Standard Deviation | mg/kg | | Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| | |
| Secondary | Fecal Calprotectin Level at Week 56 | Fecal calprotectin is an indicator of inflammation in the colon with higher levels indicative of higher levels of inflammation. | | Posted | | Mean | Standard Deviation | mg/kg | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| | |
| Secondary | Fecal Calprotectin Level at Week 8 in Participants Who Were Clinical Responders at Week 8 | Fecal calprotectin is an indicator of inflammation in the colon with higher levels indicative of higher levels of inflammation. | ITT set. A participant was a Week 8 responder if they had a clinical response at Week 8 and had evaluable data for this outcome. | Posted | | Mean | Standard Deviation | mg/kg | | Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Fecal Calprotectin Level at Week 56 in Participants Who Were Clinical Responders at Week 8 | Fecal calprotectin is an indicator of inflammation in the colon with higher levels indicative of higher levels of inflammation. | ITT set. A participant was a Week 8 responder if they had a clinical response at Week 8 and had evaluable data for this outcome. | Posted | | Mean | Standard Deviation | mg/kg | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Fecal Calprotectin Level at Week 8 in Participants Who Were Clinical Responders at Week 56 | Fecal calprotectin is an indicator of inflammation in the colon with higher levels indicative of higher levels of inflammation. Clinical response was defined as reduction in complete full Mayo score of ≥3 points and ≥30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥1 point or absolute rectal bleeding subscore of ≤1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and PGA), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | ITT set. A participant was a Week 8 responder if they had a clinical response at Week 8 and had evaluable data for this outcome | Posted | | Mean | Standard Deviation | mg/kg | | Week 8 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Fecal Calprotectin Level at Week 56 in Participants Who Were Clinical Responders at Week 56 | Fecal calprotectin is an indicator of inflammation in the colon with higher levels indicative of higher levels of inflammation. Clinical response was defined as reduction in complete full Mayo score of ≥3 points and ≥30% from Baseline (Week 0) with an accompanying decrease in rectal bleeding subscore of ≥1 point or absolute rectal bleeding subscore of ≤1 point at Week 8. The Mayo score is a tool designed to measure disease activity for ulcerative colitis. The Mayo score ranges from 0 (normal or inactive disease) to 12 (severe disease) and is calculated as the sum of 3 subscores (stool frequency, rectal bleeding, endoscopy, and physician's global assessment [PGA]), each of which ranges from 0 (normal) to 3 (severe disease). A negative change in Mayo score indicates improvement. | ITT set of participants who were clinical responders at Week 56 and had evaluable data for this outcome | Posted | | Mean | Standard Deviation | mg/kg | | Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
| |
| Secondary | Change in the Composition of Fecal Microbiota From Baseline to Week 8 and Week 56 | Composition of fecal microbiota (16S ribosomal ribonucleic acid (rRNA) gene sequencing) was measured at Week 0, Week 8, and Week 56. Fecal bacterial composition was determined using 16S sequencing. The obtained sequences were analyzed using the Ezbiocloud database and 16S microbiome pipeline to assess composition and diversity. | This endpoint was not completed due to lack of data collection. | Posted | | | | | | Week 0, Week 8, Week 56 | | | | ID | Title | Description |
|---|
| OG000 | Adalimumab | Adalimumab 160 mg at week 0, 80 mg at week 2, and then 40 mg every other week per the Korean label. |
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