Primary-outcome results across pivotal trials
Per-arm reported values from Phase 2/3 and Phase 3 trials with results posted to ClinicalTrials.gov.
| Trial | Indication | Primary endpoint | Arm | Value |
|---|---|---|---|---|
| NCT02629159 SELECT-COMPARE | Arthritis, Rheumatoid | Percentage of Participants Achieving Clinical Remission (CR) Based on DAS28(CRP) at Week 12 Week 12 | Adalimumab | 18.0 percentage of participants |
| Placebo | 6.1 percentage of participants | |||
| Upadacitinib | 28.7 percentage of participants | |||
| NCT02629159 SELECT-COMPARE | Arthritis, Rheumatoid | Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 12 Baseline and Week 12 | Adalimumab | 63.0 percentage of participants |
| Placebo | 36.4 percentage of participants | |||
| Upadacitinib | 70.5 percentage of participants | |||
| NCT02675426 SELECT-NEXT | Arthritis, Rheumatoid | Percentage of Participants Achieving Low Disease Activity (LDA) Based on DAS28(CRP) at Week 12 Week 12 | Placebo | 17.2 percentage of participants |
| Upadacitinib 15 mg | 48.4 percentage of participants | |||
| Upadacitinib 30 mg | 47.9 percentage of participants | |||
| NCT02675426 SELECT-NEXT | Arthritis, Rheumatoid | Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 12 Baseline and Week 12 | Placebo | 35.7 percentage of participants |
| Upadacitinib 15 mg | 63.8 percentage of participants | |||
| Upadacitinib 30 mg | 66.2 percentage of participants | |||
| NCT02706847 SELECT-BEYOND | Arthritis, Rheumatoid | Percentage of Participants Achieving Low Disease Activity (LDA) Based on DAS28(CRP) at Week 12 Week 12 | Placebo | 14.2 percentage of participants |
| Upadacitinib 15 mg | 43.3 percentage of participants | |||
| Upadacitinib 30 mg | 42.4 percentage of participants | |||
| NCT02706847 SELECT-BEYOND | Arthritis, Rheumatoid | Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 12 Baseline and Week 12 | Placebo | 28.4 percentage of participants |
| Upadacitinib 15 mg | 64.6 percentage of participants | |||
| Upadacitinib 30 mg | 56.4 percentage of participants | |||
| NCT02706873 SELECT-EARLY | Arthritis, Rheumatoid | Change From Baseline in Modified Total Sharp Score (mTSS) at Week 24 - Global Analysis Baseline to Week 24 | Methotrexate | 0.67 units on a scale |
| Upadacitinib 15 mg | 0.14 units on a scale | |||
| Upadacitinib 30 mg | 0.07 units on a scale | |||
| NCT02706873 SELECT-EARLY | Arthritis, Rheumatoid | Percentage of Participants Achieving Clinical Remission (CR) Based on DAS28(CRP) at Week 24 - Global Analysis Week 24 | Methotrexate | 18.5 percentage of participants |
| Upadacitinib 15 mg | 48.3 percentage of participants | |||
| Upadacitinib 30 mg | 50.0 percentage of participants | |||
| NCT02706873 SELECT-EARLY | Arthritis, Rheumatoid | Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 12 - Global Analysis Baseline and Week 12 | Methotrexate | 54.1 percentage of participants |
| Upadacitinib 15 mg | 75.7 percentage of participants | |||
| Upadacitinib 30 mg | 77.1 percentage of participants | |||
| NCT02706873 SELECT-EARLY | Arthritis, Rheumatoid | Percentage of Participants With an American College of Rheumatology 50% (ACR50) Response at Week 12 - Global Analysis Baseline and Week 12 | Methotrexate | 28.3 percentage of participants |
| Upadacitinib 15 mg | 52.1 percentage of participants | |||
| Upadacitinib 30 mg | 56.4 percentage of participants | |||
| NCT02706951 | Arthritis, Rheumatoid | Percentage of Participants Achieving Low Disease Activity (LDA) Based on DAS28(CRP) at Week 14 Week 14 | Methotrexate | 19.4 percentage of participants |
| Upadacitinib 15 mg | 44.7 percentage of participants | |||
| Upadacitinib 30 mg | 53.0 percentage of participants | |||
| NCT02706951 | Arthritis, Rheumatoid | Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 14 Baseline and week 14 | Methotrexate | 41.2 percentage of participants |
| Upadacitinib 15 mg | 67.7 percentage of participants | |||
| Upadacitinib 30 mg | 71.2 percentage of participants | |||
| NCT02720523 SELECTSUNRISE | Arthritis, Rheumatoid | Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 12 Baseline and Week 12 | Placebo | 42.9 percentage of participants |
| Upadacitinib 15 mg | 83.7 percentage of participants | |||
| Upadacitinib 30 mg | 80.0 percentage of participants | |||
| Upadacitinib 7.5 mg | 75.5 percentage of participants | |||
| NCT02819635 | Colitis, Ulcerative | Substudy 1: Percentage Of Participants Who Achieved Clinical Remission Per Adapted Mayo Score at Week 8 At Week 8 | SS1: Placebo | 0 percentage of participants |
| SS1: Upadacitinib 15 mg | 14.3 percentage of participants | |||
| SS1: Upadacitinib 30 mg | 13.5 percentage of participants | |||
| SS1: Upadacitinib 45 mg | 21.4 percentage of participants | |||
| SS1: Upadacitinib 7.5 mg | 8.5 percentage of participants | |||
| NCT02819635 | Colitis, Ulcerative | Substudy 2: Percentage Of Participants Who Achieved Clinical Remission Per Adapted Mayo Score at Week 8 At Week 8 | SS2: Placebo | 4.8 percentage of participants |
| SS2: Upadacitinib 45 mg | 26.1 percentage of participants | |||
| NCT02819635 | Colitis, Ulcerative | Substudy 3: Percentage Of Participants Who Achieved Clinical Remission Per Adapted Mayo Score at Week 52 At Week 52 | SS3: Placebo | 12.1 percentage of participants |
| SS3: UPA 15 mg | 42.3 percentage of participants | |||
| SS3: UPA 30 mg | 51.7 percentage of participants | |||
| NCT02955212 | Arthritis, Rheumatoid | Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 12 Baseline and Week 12 | Placebo | 31.4 percentage of participants |
| Upadacitinib 15 mg | 71.6 percentage of participants | |||
| NCT03086343 | Arthritis, Rheumatoid | Change From Baseline in Disease Activity Score (DAS) 28 C-Reactive Protein (CRP) at Week 12 (Non-inferiority) Baseline and Week 12 | Abatacept | -2.00 units on a scale |
| Upadacitinib 15 mg | -2.52 units on a scale | |||
| NCT03104374 SELECT - PsA 2 | Arthritis | Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 12 Baseline and Week 12 | Placebo | 24.1 percentage of participants |
| Upadacitinib 15 mg | 56.9 percentage of participants | |||
| Upadacitinib 30 mg | 63.8 percentage of participants | |||
| NCT03104400 SELECT - PsA 1 | Arthritis | Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 12 Baseline and Week 12 | Adalimumab 40 mg | 65.0 percentage of participants |
| Placebo | 36.2 percentage of participants | |||
| Upadacitinib 15 mg | 70.6 percentage of participants | |||
| Upadacitinib 30 mg | 78.5 percentage of participants | |||
| NCT03345836 | Crohn Disease | Number of Participants With Adverse Events From first dose of study drug until 30 days following last dose of study drug (up to approximately 28 weeks) | Part 1 (Double-blind): Placebo | 112 Participants |
| Part 1 (Double-blind): Upadacitinib 45 mg | 221 Participants | |||
| Part 2 (Open-label): Upadacitinib 45 mg | 86 Participants | |||
| Part 3 (Extended Treatment DB): Upadacitinib 30 mg From Part 1 DB Upadacitinib 45 mg | 45 Participants | |||
| Part 3 (Extended Treatment DB): Upadacitinib 45 mg From Part 1 DB Placebo | 53 Participants | |||
| Part 3 (Extended Treatment OL): Upadacitinib 30 mg From Part 2 OL Upadacitinib 45 mg | 9 Participants | |||
| NCT03345836 | Crohn Disease | Percentage of Participants With Clinical Remission Per Crohn's Disease Activity Index (CDAI) at Week 12 Week 12 | Part 1 (Double Blind): Placebo | 21.1 percentage of participants |
| Part 1 (Double Blind): Upadacitinib 45 mg | 38.9 percentage of participants | |||
| NCT03345836 | Crohn Disease | Percentage of Participants With Endoscopic Response at Week 12 Baseline to Week 12 | Part 1 (Double Blind): Placebo | 3.5 percentage of participants |
| Part 1 (Double Blind): Upadacitinib 45 mg | 34.6 percentage of participants | |||
| NCT03345849 U-EXCEL | Crohn Disease | Percentage of Participants With Clinical Remission Per Crohn's Disease Activity Index (CDAI) at Week 12 Week 12 | Placebo | 29.1 percentage of participants |
| Upadacitinib 45 mg QD | 49.5 percentage of participants | |||
| NCT03345849 U-EXCEL | Crohn Disease | Percentage of Participants With Clinical Remission Per Patient-Reported Outcomes (PROs) at Week 12 Week 12 | Placebo | 22.2 percentage of participants |
| Upadacitinib 45 mg QD | 50.7 percentage of participants | |||
| NCT03345849 U-EXCEL | Crohn Disease | Percentage of Participants With Endoscopic Response at Week 12 Baseline and Week 12 | Placebo | 13.1 percentage of participants |
| Upadacitinib 45 mg QD | 45.5 percentage of participants | |||
| NCT03568318 AD Up | Dermatitis, Atopic | Main Study: Percentage of Participants Achieving at Least a 75% Reduction in Eczema Area and Severity Index Score (EASI 75) From Baseline at Week 16 Baseline and Week 16 | Placebo + Topical Corticosteroids | 26.4 percentage of participants |
| Upadacitinib 15 mg + Topical Corticosteroids | 64.6 percentage of participants | |||
| Upadacitinib 30 mg + Topical Corticosteroids | 77.1 percentage of participants | |||
| NCT03568318 AD Up | Dermatitis, Atopic | Main Study: Percentage of Participants Achieving Validated Investigator Global Assessment for Atopic Dermatitis (vIGA-AD) of 0 or 1 With a Reduction From Baseline of ≥ 2 Points at Week 16 Baseline and Week 16 | Placebo + Topical Corticosteroids | 10.9 percentage of participants |
| Upadacitinib 15 mg + Topical Corticosteroids | 39.6 percentage of participants | |||
| Upadacitinib 30 mg + Topical Corticosteroids | 58.6 percentage of participants | |||
| NCT03569293 Measure Up 1 | Dermatitis, Atopic | Main Study: Percentage of Participants Achieving at Least a 75% Reduction in Eczema Area and Severity Index Score (EASI 75) From Baseline at Week 16 Baseline and Week 16 | Placebo | 16.3 percentage of participants |
| Upadacitinib 15 mg QD | 69.6 percentage of participants | |||
| Upadacitinib 30 mg QD | 79.7 percentage of participants | |||
| NCT03569293 Measure Up 1 | Dermatitis, Atopic | Main Study: Percentage of Participants Achieving Validated Investigator Global Assessment for Atopic Dermatitis (vIGA-AD) of 0 or 1 With a Reduction From Baseline of ≥ 2 Points at Week 16 Baseline and Week 16 | Placebo | 8.4 percentage of participants |
| Upadacitinib 15 mg QD | 48.1 percentage of participants | |||
| Upadacitinib 30 mg QD | 62.0 percentage of participants | |||
| NCT03607422 | Dermatitis, Atopic | Main Study: Percentage of Participants Achieving at Least a 75% Reduction in Eczema Area and Severity Index Score (EASI 75) From Baseline at Week 16 Baseline and Week 16 | Placebo | 13.3 percentage of participants |
| Upadacitinib 15 mg QD | 60.1 percentage of participants | |||
| Upadacitinib 30 mg QD | 72.9 percentage of participants | |||
| NCT03607422 | Dermatitis, Atopic | Main Study: Percentage of Participants Achieving Validated Investigator Global Assessment for Atopic Dermatitis (vIGA-AD) of 0 or 1 With a Reduction From Baseline of ≥ 2 Points at Week 16 Baseline and Week 16 | Placebo | 4.7 percentage of participants |
| Upadacitinib 15 mg QD | 38.8 percentage of participants | |||
| Upadacitinib 30 mg QD | 52.0 percentage of participants | |||
| NCT03653026 U-Accomplish | Colitis, Ulcerative | Percentage of Participants Who Achieved Clinical Remission Per Adapted Mayo Score at Week 8 Week 8 | Placebo | 4.1 percentage of participants |
| Upadacitinib 45 mg | 33.5 percentage of participants | |||
| NCT03725202 SELECT-GCA | Giant Cell Arteritis | Percentage of Participants Achieving Sustained Remission at Week 52 From Week 12 to Week 52 | 15 mg Upadacitinib + 26-week CS Taper | 46.4 percentage of participants |
| 7.5 mg Upadacitinib + 26-week CS Taper | 41.1 percentage of participants | |||
| Placebo + 52-week CS Taper | 29.0 percentage of participants | |||
| NCT03738397 Heads Up | Dermatitis, Atopic | Percentage of Participants Achieving a 75% Reduction From Baseline in Eczema Area and Severity Index Score (EASI 75) at Week 16 Baseline and Week 16 | Dupilumab 300 mg EOW | 62.6 percentage of participants |
| Upadacitinib 30 mg QD | 72.4 percentage of participants | |||
| NCT04169373 SELECT-AXIS 2 | Axial Spondyloarthritis | Study 1: Percentage of Participants Achieving Assessment of SpondyloArthritis International Society 40 (ASAS40) Response at Week 14 Baseline and Week 14 | Study 1: Placebo | 18.2 percentage of participants |
| Study 1: Upadacitinib 15 mg | 44.5 percentage of participants | |||
| NCT04169373 SELECT-AXIS 2 | Axial Spondyloarthritis | Study 2: Percentage of Participants Achieving an ASAS40 Response at Week 14 Baseline and Week 14 | Study 2: Placebo | 22.5 percentage of participants |
| Study 2: Upadacitinib 15 mg | 44.9 percentage of participants | |||
| NCT04195698 | Dermatitis, Atopic | Number of Participants With Treatment-Emergent Adverse Events UPA/UPA arm: BL visit in Lead-In M16-046 to last dose in Long-Term Extension M19-850 (median time on follow-up is 536 days); DUPI/UPA arm: BL visit in Long-Term Extension M19-850 to last dose plus a 30-day follow-up (median time on follow-up is 399 days). | DUPI 300mg to UPA 30mg | 205 Participants |
| DUPI 300mg to UPA 30mg | 12 Participants | |||
| DUPI 300mg to UPA 30mg | 14 Participants | |||
| UPA 30mg to UPA 30mg | 17 Participants | |||
| UPA 30mg to UPA 30mg | 18 Participants | |||
| UPA 30mg to UPA 30mg | 223 Participants | |||
| NCT04195698 | Dermatitis, Atopic | Number of Participants With Treatment-Emergent Adverse Events of Special Interest (AESI) UPA/UPA arm: BL visit in Lead-In M16-046 to last dose in Long-Term Extension M19-850 (median time on follow-up is 536 days); DUPI/UPA arm: BL visit in Long-Term Extension M19-850 to last dose plus a 30-day follow-up (median time on follow-up is 399 days). | DUPI 300mg to UPA 30mg | 6 Participants |
| DUPI 300mg to UPA 30mg | 0 Participants | |||
| DUPI 300mg to UPA 30mg | 4 Participants | |||
| DUPI 300mg to UPA 30mg | 19 Participants | |||
| DUPI 300mg to UPA 30mg | 1 Participants | |||
| DUPI 300mg to UPA 30mg | 0 Participants | |||
| DUPI 300mg to UPA 30mg | 26 Participants | |||
| DUPI 300mg to UPA 30mg | 31 Participants | |||
| DUPI 300mg to UPA 30mg | 1 Participants | |||
| DUPI 300mg to UPA 30mg | 0 Participants | |||
| DUPI 300mg to UPA 30mg | 7 Participants | |||
| DUPI 300mg to UPA 30mg | 0 Participants | |||
| DUPI 300mg to UPA 30mg | 0 Participants | |||
| DUPI 300mg to UPA 30mg | 7 Participants | |||
| DUPI 300mg to UPA 30mg | 10 Participants | |||
| DUPI 300mg to UPA 30mg | 0 Participants | |||
| DUPI 300mg to UPA 30mg | 0 Participants | |||
| UPA 30mg to UPA 30mg | 8 Participants | |||
| UPA 30mg to UPA 30mg | 0 Participants | |||
| UPA 30mg to UPA 30mg | 5 Participants | |||
| UPA 30mg to UPA 30mg | 1 Participants | |||
| UPA 30mg to UPA 30mg | 44 Participants | |||
| UPA 30mg to UPA 30mg | 0 Participants | |||
| UPA 30mg to UPA 30mg | 0 Participants | |||
| UPA 30mg to UPA 30mg | 8 Participants | |||
| UPA 30mg to UPA 30mg | 4 Participants | |||
| UPA 30mg to UPA 30mg | 0 Participants | |||
| UPA 30mg to UPA 30mg | 25 Participants | |||
| UPA 30mg to UPA 30mg | 0 Participants | |||
| UPA 30mg to UPA 30mg | 0 Participants | |||
| UPA 30mg to UPA 30mg | 15 Participants | |||
| UPA 30mg to UPA 30mg | 0 Participants | |||
| UPA 30mg to UPA 30mg | 0 Participants | |||
| UPA 30mg to UPA 30mg | 8 Participants | |||
| NCT04195698 | Dermatitis, Atopic | Percentage of Participants With Potentially Clinically Important (PCI) Laboratory Values as Assessed by the Investigator From Baseline to 30 days following last dose of study drug (Week 52) | DUPI 300mg to UPA 30mg | 0 percentage of participants |
| DUPI 300mg to UPA 30mg | 1.3 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 3.4 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 3.4 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0.8 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0.4 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0.4 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 4.2 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 3.8 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 8.0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 1.7 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 1.7 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 1.3 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0.5 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0.5 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 2.5 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 1.3 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0.4 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 2.9 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 1.3 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0.8 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.8 percentage of participants | |||
| UPA 30mg to UPA 30mg | 3.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.8 percentage of participants | |||
| UPA 30mg to UPA 30mg | 1.3 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 3.8 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 3.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 1.3 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 3.8 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 1.3 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 1.3 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 8.1 percentage of participants | |||
| UPA 30mg to UPA 30mg | 5.1 percentage of participants | |||
| UPA 30mg to UPA 30mg | 13.1 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.8 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 1.3 percentage of participants | |||
| UPA 30mg to UPA 30mg | 1.3 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 1.3 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.4 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 5.1 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 5.1 percentage of participants | |||
| NCT04195698 | Dermatitis, Atopic | Percentage of Participants With Potentially Clinically Important (PCI) Vital Sign Measurements and Physical Examination Findings as Assessed by the Investigator From Baseline to 30 days following last dose of study drug (Week 52) | DUPI 300mg to UPA 30mg | 2.5 percentage of participants |
| DUPI 300mg to UPA 30mg | 0.4 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0.4 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 2.1 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 1.7 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 0 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 5.5 percentage of participants | |||
| DUPI 300mg to UPA 30mg | 22.5 percentage of participants | |||
| UPA 30mg to UPA 30mg | 39.0 percentage of participants | |||
| UPA 30mg to UPA 30mg | 4.7 percentage of participants | |||
| UPA 30mg to UPA 30mg | 0.8 percentage of participants | |||
| UPA 30mg to UPA 30mg | 5.5 percentage of participants | |||
| UPA 30mg to UPA 30mg | 7.6 percentage of participants | |||
| UPA 30mg to UPA 30mg | 1.3 percentage of participants | |||
| UPA 30mg to UPA 30mg | 2.1 percentage of participants | |||
| UPA 30mg to UPA 30mg | 9.3 percentage of participants | |||
| NCT05601882 Level Up | Dermatitis, Atopic | Percentage of Participants Achieving a ≥ 90% Reduction From Baseline in Eczema Area and Severity Index Score (EASI 90) and Worst Pruritus Numerical Rating Scale of 0 or 1 (WP-NRS 0/1) at Week 16 Baseline and Week 16 | Dupilumab (Period 1) | 8.9 percentage of participants |
| Upadacitinib (Period 1) | 19.9 percentage of participants |