Study name, year, and NCT | Study design, country | Intervention | Study sample size, n | Age (years), mean (SD) | Male, % | Disease duration (years), mean (SD) | Biologic experience, % | Employed, % | Psoriasis, % | PASI, mean (SD) | DAS28-CRP, mean (SD) | WPAI version |
---|---|---|---|---|---|---|---|---|---|---|---|---|
KEEPsAKE 1 2022 (NCT03675308) [23] | RCT, Multiple | Risankizumab 150 mg | 483 | 51.3 (12.2) | 52.2 | 7.1 (7.0) | 0 | –a | 100 | 10.9 (10.1) | – | WPAI:PsA |
Placebo | 481 | 51.2 (12.1) | 48.6 | 7.1 (7.7) | 0 | 100 | 10.0 (10.4) | – | ||||
KEEPsAKE 2 2022 (NCT03671148) [24] | RCT, Multiple | Risankizumab 150 mg | 224 | 53.1 (12.5) | 44.6 | 8.2 (8.2) | 46.9 | –a | 54.9b | 7.7 (6.7) | – | WPAI:PsA |
Placebo | 219 | 52.7 (12.6) | 45.2 | 8.2 (8.3) | 46.1 | 54.3b | 8.4 (9.9) | – | ||||
BE OPTIMAL 2022 (NCT03895203) [25] (data on file) | RCT, Multiple | Bimekizumab 160Â mg | 431 | 48.5 (12.6) | 46.6 | 6.0 (7.3) | 0 | 63 | 50.3b | 8.2 (6.8) | 3.8 (0.9) | WPAI:SHP |
Adalimumab 40Â mg | 140 | 49.0 (12.8) | 50.7 | 6.1 (6.8) | 0 | 64 | 48.6b | 8.6 (7.6) | 3.7 (0.9) | |||
Placeboe | 281 | 48.7 (11.7) | 45.2 | 5.6 (6.5) | 0 | 67 | 49.8b | 7.9 (5.6) | 3.8 (1.0) | |||
SELECT-PsA 1 2021 (NCT03104400) [22] | RCT, Multiple | Upadacitinib 15 mg QD | 429 | 51.6 (12.2) | 44.5 | 6.2 (7.4) | 0 | 58a | – | 9.8 (10.0) | – | WPAI |
Adalimumab 40 mg EOW | 429 | 51.4 (12.0) | 48.2 | 5.9 (7.1) | 0 | – | 9.4 (8.5) | – | ||||
Placebo | 423 | 50.4 (12.2) | 51.1 | 6.2 (7.0) | 0 | – | 11.2 (11.4) | – | ||||
DISCOVER-2 2021 (NCT03158285) [26] | RCT, Multiple | Guselkumab 100 mg Q4W | 245 | 46.0 (12.0) | 58.0 | 5.5 (5.9) | 0 | 62 | 100 | 10.8 (11.7) | – | WPAI:PsA |
Guselkumab 100 mg Q8W | 248 | 45.0 (12.0) | 52.0 | 5.1 (5.5) | 0 | 100 | 9.7 (11.7) | – | ||||
Placebo | 246 | 46.0 (12.0) | 48.0 | 5.8 (5.6) | – | 100 | 9.3 (9.8) | – | ||||
SELECT-PsA 2 2021 (NCT03104374) [27] | RCT, Multiple | Upadacitinib 15 mg QD | 211 | 53.0 (12.0) | 46.4 | 9.6 (8.4) | 100 | –a | – | 10.1 (9.2) | – | WPAI |
Placebo | 212 | 54.1 (11.5) | 43.4 | 11.0 (10.3) | 100 | – | 11.7 (11.4) | – | ||||
FUTURE 1 2017 (NCT01392326) [28] | RCT, Multiple | Secukinumab 150 mg Q4W | 202 | 49.6 (11.8) | 47.5 | – | 29.2c | 51 | 53.5b | 15.6 (13.9) | 4.8 (1.1) | WPAI:GH |
Placebo | 202 | 48.5 (11.2) | 47.5 | – | 61 | 54.0b | 15.1 (11.6) | 4.9 (1.1) | ||||
RCT, Multiple | Ixekizumab 80Â mg Q4W | 122 | 52.6 (13.6) | 52.0 | 11 (9.6) | 100 | 53 | 97.0d | 6.4 (7.9) | 5.1 (1.1) | WPAI:SHP | |
Ixekizumab 80Â mg Q2W | 123 | 51.7 (11.9) | 41.0 | 9.9 (7.4) | 100 | 57 | 92.0d | 6.2 (8.7) | 5.1 (1.1) | |||
Placebo | 118 | 51.5 (10.4) | 47.0 | 9.2 (7.3) | 100 | 44.9 | – | 5.2 (6.3) | 5.0 (1.1) | |||
RCT, Multiple | Adalimumab 40Â mg Q2W | 101 | 48.6 (12.4) | 50.5 | 6.9 (7.5) | 0 | 61 | 96.0d | 5.5 (6.5) | 4.9 (1.0) | WPAI:SHP | |
Ixekizumab 80Â mg Q4W | 107 | 49.1 (10.1) | 42.1 | 6.2 (6.4) | 0 | 68 | 93.5d | 6.9 (6.6) | 5.0 (1.0) | |||
Ixekizumab 80Â mg Q2W | 103 | 49.8 (12.6) | 46.6 | 7.2 (8.0) | 0 | 60 | 92.2d | 6.0 (7.0) | 5.0 (1.0) | |||
Placebo | 106 | 50.6 (12.3) | 45.3 | 6.3 (6.9) | 0 | 45.3 | – | 6.2 (7.5) | 4.9 (1.0) | |||
FUTURE 2 2015 (NCT01752634) [32] | RCT, Multiple | Secukinumab 300 mg Q4W | 100 | 46.9 (12.6) | 51.0 | 7.4 (7.5) | 33.0c | –a | 41.0b | 11.9 (8.4)b | 4.8 (1.1) | WPAI:GH |
Secukinumab 150Â mg Q4W | 100 | 46.5 (11.7) | 55.0 | 6.5 (8.2) | 37.0c | 58.0b | 16.2 (14.3)b | 4.9 (1.1) | ||||
Placebo | 98 | 49.9 (12.5) | 39.8 | 7.3 (7.8) | 35.7c | 43.9b | 11.6 (8.3) | 4.7 (1.0) | ||||
Nakagawa 2019 (NCT02414633) [33] | Prospective observational, Japan | Adalimumab 40 mg, 80 mg | 106 | 49.3 (10.7) | 72.6 | – | 10.4 | 100 | – | 9.0 (8.6) | 3.8 (1.3) | WPAI:PsA v2 |
Corrona 2020 (NCT02530268) [21] | Prospective observational, United States | Secukinumab 150 mg, 300 mg | 100 | 51.6 (11.6) | 54.3 | 7.0 (7.0) | 83.0 | – | – | – | – | WPAI |