Table 2.
Agent (route of admission) | Target mechanism | Outcome (placebo) |
---|---|---|
Secukinumab (subcutaneous) | IL-17 |
Casseres et al.: HiSCR week 20: 67% SUNSHINE: HiSCR week 16: 45% (versus 34%) SUNRISE: HiSCR week 16: 42–46% (versus 31%) |
Tofacitinib (oral) | JAK | “Improvement” in two patient case series |
Povorcitinib (oral) | JAK |
First phase 2 trial: HiSCR week 8: 43% Second phase 2 trial: HiSCR week 8: 88% (versus 57%) |
Bermekimab (subcutaneous) | IL-1α |
TNF-α failure: HiSCR week 12: 63% TNF-α naive: HiSCR week 12: 61% |
IFX-1 (intravenous) | C5a | HiSCR week 16: non-superior to placebo (47%) |
Apremilast (oral) | PDE4 | HiSCR week 16: 53% |
Metformin monotherapy (oral) | Antiinflammatory effects | Subjective clinical response 12 months: 68% |
Risankizumab (subcutaneous) |
IL-23α | HiSCR week 16: non-superior to placebo; 43–47% (versus 42%) |
IL Interleukin, JAK Janus kinase, PDE4 Phosphodiesterase-4, C5a Complement 5a, HiSCR Hidradenitis Suppurativa Clinical Response, TNF Tumor necrosis factor