Table 4.
Study drug | Study analysis | Dose | Mean % improvement in NAPSI |
---|---|---|---|
Infliximab, TNF‐α inhibitor16 |
Phase 3, RCT Retrospective |
5 mg Q8W | W50, 67.8% |
Etanercept, TNF‐α inhibitor15 |
Randomized, open‐label Post hoc |
25 mg biw | W54, 51.0% |
Ustekinumab, IL‐2/23 inhibitor18 |
Phase 2/3, RCT Secondary endpoint |
45 mg and 90 mg Q12W |
W64, 56.6% (45 mg) W64, 67.8% (90 mg) |
Ixekizumab, IL‐17A inhibitor19 |
Phase 2, RCT Post hoc |
120 mg Q4W | W48, 75.4% |
Ixekizumab, IL‐17A inhibitor20 |
Phase 3, RCT Subgroup |
80 mg Q4W | W60, 81.8% |
Tofacitinib, JAK inhibitor21 |
Phase 3, RCT Post hoc |
5 mg and 10 mg bid |
W52, 65.6% (5 mg) W52, 75.5% (10 mg) |
bid, twice daily; biw, twice weekly; eow, every other week; NAPSI, Nail Psoriasis Severity Index; Ps, psoriasis; RCT, randomized controlled trial; QnW, every n week(s); W, week.