Extrapolating the speed of psoriasis clearance: Head-to-head agents in clinical trials

Authors

  • Creighton Pfau AT Still University School of Osteopathic Medicine Arizona, Mesa, Arizona. Author
  • Katie K Lovell Center for Dermatology Research, Department of Dermatology, Wake Forest University School of Medicine, Winston-Salem, North Carolina. Author
  • Hanna Ozbeki AT Still University School of Osteopathic Medicine Arizona, Mesa, Arizona. Author
  • Steven R. Feldman Center for Dermatology Research, Department of Dermatology, Wake Forest University School of Medicine, Winston-Salem, North Carolina. , Department of Dermatology, Wake Forest University School of Medicine, Winston-Salem, North Carolina. , Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, North Carolina , Department of Social Sciences & Health Policy, Wake Forest University School of Medicine, Winston-Salem, North Carolina. Author

DOI:

https://doi.org/10.25251/t1b8ft53

Keywords:

psoriasis, biologics, trials, PASI, speed of response

Abstract

Background: Biologic therapies targeting interleukin-17 (IL-17) and interleukin-23 (IL-23) pathways have transformed psoriasis management, with IL-17 inhibitors widely regarded as achieving faster clearance. However, the clinical significance of differences in clearance times remains unclear.

Objective: To compare time to achieve a 75% reduction in the Psoriasis Area and Severity Index (PASI75) between IL-17 and IL-23 inhibitors using data from head-to-head clinical trials.

Methods: A PubMed search identified trials reporting PASI75 response times for IL-17 and IL-23 inhibitors. Graphs from 12 studies were analyzed using Engauge Digitizer Software to estimate the time until half of participants reached PASI75.

Results: IL-17 inhibitors achieved PASI75 faster than IL-23 inhibitors, with average response times of 4.5 weeks versus 7 weeks, respectively. The fastest IL-17 agent (bimekizumab) reached PASI75 in 2.5 weeks, while the fastest IL-23 agent (risankizumab) required 5.5 weeks. Differences between classes were smaller than anticipated, particularly for newer IL-23 inhibitors targeting the p19 subunit. Limitations: PASI75 timepoints were estimated from published graphs, introducing potential measurement error.

Conclusion: IL-17 inhibitors generally achieve faster psoriasis clearance than IL-23 inhibitors, but the clinical relevance of this difference is limited. Safety and long-term efficacy profiles should guide treatment selection, highlighting the importance of personalized patient care.

References

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Published

05/09/2026