| Primary | Percentage of Participants Achieving a 75% Reduction in the Psoriasis Area and Severity Index (PASI75) at Week 12 | Combined assessment of lesion severity and area affected into single score; range equals (=) 0 (no disease) to 72 (maximal disease). Body divided into 4 sections=head, upper/lower limbs, trunk; each area scored by itself and scores combined for final PASI. For each section percent area of skin involved was estimated: 0 (0%) to 6 (90-100%) and severity estimated by clinical signs of erythema, induration, scaling; ranged 0-4: 0=none, 1=slight, 2=moderate, 3=marked, 4=very marked. Final PASI=sum of severity parameters for each section*area score*weighing factor (head=0.1, upper limbs=0.2, trunk=0.3, lower limbs=0.4) summed over all sections. | | Posted | | Number | | percentage of participants | | Week 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Primary | Percentage of Participants Achieving a Physician's Global Assessment (PGA) Response of "Clear" or "Almost Clear" at Week 12 | PGA psoriasis is scored on a 5-point scale, reflecting a global consideration of the erythema, induration and scaling across all psoriatic lesions. PGA of Psoriasis scale ranges from 0 (no psoriasis) to 4 (severe disease). ‘Clear’ and “Almost clear’ includes all participants who were scored as a 0 or 1. | | Posted | | Number | | percentage of participants | | Week 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Psoriasis Area and Severity Index (PASI) Score by Visit | Combined assessment of lesion severity and area affected into single score. Body was divided into 4 sections: head, arms, trunk, legs. For each section, percent area of skin involved was estimated: 0=0% to 6=90â€"100%. Severity was estimated by clinical signs: erythema, induration, desquamation; scale: 0= none to 4= maximum. Final PASI = sum of severity parameters for each section*area score*weight of section (head: 0.1, arms: 0.2, body: 0.3, legs: 0.4) summed over all sections; total possible score range: 0= no disease to 72= maximal disease. | FAS; n (number) =number of participants with nonmissing observations at the specified visit. | Posted | | Mean | Standard Error | units on a scale | | Baseline and Weeks 1, 2, 4, and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Change From Baseline in PASI by Visit | Combined assessment of lesion severity and area affected into single score. Body was divided into 4 sections: head, arms, trunk, legs. For each section, percent area of skin involved was estimated: 0=0% to 6=90â€"100%. Severity was estimated by clinical signs: erythema, induration, desquamation; scale: 0= none to 4= maximum. Final PASI = sum of severity parameters for each section*area score*weight of section (head: 0.1, arms: 0.2, body: 0.3, legs: 0.4) summed over all sections; total possible score range: 0= no disease to 72= maximal disease. | Because Cohort 2 of the study was not conducted and Cohort 1 had a limited number of participants, the analyses were simplified and this analysis was not performed. | Posted | | | | | | Weeks 1, 2, 4 and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Percent Change From Baseline in PASI by Visit | Combined assessment of lesion severity and area affected into single score. Body was divided into 4 sections: head, arms, trunk, legs. For each section, percent area of skin involved was estimated: 0= 0% to 6= 90â€"100%. Severity was estimated by clinical signs: erythema, induration, desquamation; scale: 0= none to 4= maximum. Final PASI = sum of severity parameters for each section*area score*weight of section (head: 0.1, arms: 0.2, body: 0.3, legs: 0.4) summed over all sections; total possible score range: 0= no disease to 72= maximal disease. | FAS; n=number of participants with nonmissing observations at the specified visit. | Posted | | Mean | Standard Error | percent change from baseline | | Weeks 1, 2, 4, and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Percentage of Participants Achieving a PASI75 Response at Weeks 1, 2, and 4 | Combined assessment of lesion severity and area affected into single score; range=0 (no disease) to 72 (maximal disease). Body divided into 4 sections=head, upper/lower limbs, trunk; each area scored by itself and scores combined for final PASI. For each section percent area of skin involved was estimated: 0 (0%) to 6 (90-100%) and severity estimated by clinical signs of erythema, induration, scaling; ranged 0-4: 0=none, 1=slight, 2=moderate, 3=marked, 4=very marked. Final PASI=sum of severity parameters for each section*area score*weighing factor (head=0.1, upper limbs=0.2, trunk=0.3, lower limbs=0.4) summed over all sections. | | Posted | | Number | | percentage of participants | | Weeks 1, 2, and 4 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Change From Baseline in PGA Score by Visit | PGA psoriasis is scored on a 5-point scale, reflecting a global consideration of the erythema, induration, and scaling across all psoriatic lesions. PGA of Psoriasis scale ranges from 0 (no psoriasis) to 4 (severe disease). The severity scores of 3 components (erythema, induration, and scaling) are averaged and rounded to the nearest whole number to determine the PGA score. | FAS; n=number of participants with nonmissing observations at the specified visit. | Posted | | Mean | Standard Error | units on a scale | | Weeks 1, 2, 4, and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Percentage of Participants in Each PGA Category at Various Timepoints by Baseline Category | | Because Cohort 2 of the study was not conducted and Cohort 1 had a limited number of participants, the analyses were simplified and this analysis was not performed. | Posted | | | | | | Baseline and Weeks 1, 2, 4, and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Percentage of Participants by PGA Response Category and Timepoint | PGA psoriasis is scored on a 5-point scale, reflecting a global consideration of the erythema, induration and scaling across all psoriatic lesions. PGA of Psoriasis scale ranges from 0 (no psoriasis) to 4 (severe disease). Response category scores: 0=clear; 1=almost clear; 2=mild; 3=moderate; and 4=severe. The severity scores of 3 components (erythema, induration, and scaling) are averaged and rounded to the nearest whole number to determine the PGA score. | FAS; n=number of participants with nonmissing observations at the specified visit. | Posted | | Number | | percentage of participants | | Baseline and Weeks 1, 2, 4, and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Body Surface Area (BSA) | Assessment of BSA with psoriasis was performed separately for 4 body regions: head and neck, upper limbs, trunk (including axillae and groin), and lower limbs (including buttocks). The percent surface area with psoriasis was estimated by means of the handprint method, where the full palmar hand of the participant (ie, the participant's fully extended palm, fingers and thumb together) represents approximately 1% of the total BSA. The number of handprints of psoriatic skin in a body region can be used to determine the extent (%) to which a body regions is involved with psoriasis. In each body region, the percent body region surface area with psoriasis is multiplied by the Body Region Weighting (head and neck=10%, upper limbs=5%, trunk [including axillae and groin]=3.33% and lower limbs [including buttocks]=2.5%). BSA (%)=0.1Sh + 0.2Sh+0.3St+0.4Sl, where S=body region suface area with psoriasis: h=head; u=upper limbs; t=trunk; l=lower limbs. | FAS; n=number of participants with nonmissing observations at the specified visit. | Posted | | Mean | Standard Error | % BSA | | Baseline and Weeks 1, 2, 4, and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Change From Baseline in BSA | Assessment of BSA with psoriasis was performed separately for 4 body regions: head and neck, upper limbs, trunk (including axillae and groin), and lower limbs (including buttocks). The percent surface area with psoriasis was estimated by means of the handprint method, where the full palmar hand of the participant (ie, the participant's fully extended palm, fingers and thumb together) represents approximately 1% of the total BSA. The number of handprints of psoriatic skin in a body region can be used to determine the extent (%) to which a body regions is involved with psoriasis. In each body region, the percent body region surface area with psoriasis is multiplied by the Body Region Weighting (head and neck=10%, upper limbs=5%, trunk [including axillae and groin]=3.33% and lower limbs [including buttocks]=2.5%). BSA (%)=0.1Sh + 0.2Sh+0.3St+0.4Sl, where S=body region suface area with psoriasis: h=head; u=upper limbs; t=trunk; l=lower limbs. | Because Cohort 2 of the study was not conducted and Cohort 1 had a limited number of participants, the analyses were simplified and this analysis was not performed. | Posted | | | | | | Weeks 1, 2, 4, and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Percent Change From Baseline in BSA | Assessment of BSA with psoriasis was performed separately for 4 body regions: head and neck, upper limbs, trunk (including axillae and groin), and lower limbs (including buttocks). The percent surface area with psoriasis was estimated by means of the handprint method, where the full palmar hand of the participant (ie, the participant's fully extended palm, fingers and thumb together) represents approximately 1% of the total BSA. The number of handprints of psoriatic skin in a body region can be used to determine the extent (%) to which a body regions is involved with psoriasis. In each body region, the percent body region surface area with psoriasis is multiplied by the Body Region Weighting (head and neck=10%, upper limbs=5%, trunk [including axillae and groin]=3.33% and lower limbs [including buttocks]=2.5%). BSA (%)=0.1Sh + 0.2Sh+0.3St+0.4Sl, where S=body region suface area with psoriasis: h=head; u=upper limbs; t=trunk; l=lower limbs. | FAS; n=number of participants with nonmissing observations at the specified visit. | Posted | | Mean | Standard Error | percent change from baseline | | Weeks 1, 2, 4, and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Itch Severity Item (ISI) Score by Visit | The severity of itch (pruritus) due to psoriasis was assessed using the ISI, a single-item, horizontal numeric rating scale. Participants were asked to rate "your worst itching due to psoriasis over the past 24 hours" on a numeric rating scale anchored by the terms "No itching" (0) and "Worst possible itching" (10) at the ends. the baseline is defined as the average of all available diary entries before Baseline/Day 1 and the in-clinic measurement on Baseline/day 1. Week 1 is the mean of daily values of study days 2 to 8 and Week 2 is the mean of daily values of study days 9 to 15. | FAS; n=number of participants with nonmissing observations at the specified visit. | Posted | | Mean | Standard Error | units on a scale | | Baseline and Weeks 1, 2, 4, and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Change From Baseline in ISI by Visit | ISI, a single-item, horizontal numeric rating scale. Participants were asked to rate "your worst itching due to psoriasis over the past 24 hours" on a numeric rating scale anchored by the terms "No itching" (0) and "Worst possible itching" (10) at the ends. The baseline is defined as the average of all available diary entries before Baseline/Day 1 and the in-clinic measurement on Baseline/Day 1. Week 1 is the mean of daily values of study days 2 to 8 and Week 2 is the mean of daily values of study days 9 to 15. A negative value indicates an improvement. | FAS; n=number of participants with nonmissing observations at the specified visit. | Posted | | Mean | Standard Error | units on a scale | | Weeks 1, 2, 4 and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Target Plaque Severity Score (TPSS) by Visit | Target lesions were selected at baseline and followed for the duration of the study. Each target lesion was scored by the investigator on severity of erythema, induration, and scaling according to a 5-point (0 to 4) severity scale with a maximum sum score for a plaque of 12. The TPSS was calculated as the sum of the scores for erythema, induration, and scaling; the score can vary in increments of 1 unit from 0 to 12. | FAS; n=number of participants with nonmissing observations at the specified visit. | Posted | | Mean | Standard Error | score on a scale | | Baseline and Weeks 1, 2, 4, and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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| Secondary | Percent Change From Baseline in TPSS by Visit | Target lesions were selected at baseline and followed for the duration of the study. Each target lesion was scored by the investigator on severity of erythema, induration, and scaling according to a 5-point (0 to 4) severity scale with a maximum sum score for a plaque of 12. The TPSS was calculated as the sum of the scores for erythema, induration, and scaling; the score can vary in increments of 1 unit from 0 to 12. A negative value indicated improvment. | FAS; n=number of participants with nonmissing observations at the specified visit. | Posted | | Mean | Standard Error | percent change from baseline | | Weeks 1, 2, 4, and 12 | | | | ID | Title | Description |
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| OG000 | Tofacitinib 10 mg BID | Participants received tofacitinib tablets, 10 mg, orally, BID for 12 weeks. | | OG001 | Placebo | Participants received matching placebo tablets, orally, BID for 12 weeks. |
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