All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a Healthcare Professional.

  TRANSLATE

The pso Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the pso Hub cannot guarantee the accuracy of translated content. The pso and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.

The PsOPsA Hub is supported by educational grants. All educational content is developed independently by SES in collaboration with our expert steering committee, with no input or influence from financial supporters. We would like to express our gratitude to the following companies for their support: • UCB: For website development, launch, and ongoing maintenance. • UCB: For educational content and news updates.

Now you can support HCPs in making informed decisions for their patients

Your contribution helps us continuously deliver expertly curated content to HCPs worldwide. You will also have the opportunity to make a content suggestion for consideration and receive updates on the impact contributions are making to our content.

Find out more

LIMMitless long-term results: Continuous risankizumab in moderate-to-severe plaque psoriasis

By Sheetal Bhurke

Share:

Oct 14, 2025

Learning objective: After reading this article, learners will be able to cite a new clinical development in plaque psoriasis.


Long-term results of the phase III, open-label extension of the LIMMitless trial (NCT03047395) were published by Papp et al. in the American Journal of Clinical Dermatology. This trial evaluated the efficacy and safety of 150 mg risankizumab every 12 weeks over a duration of 324 weeks in 897 patients with moderate-to-severe plaque psoriasis (661 patients completed the study). 

Key data: At Week 324, risankizumab showed lower cumulative rates of serious adverse events (SAEs), at 6.7 vs 9.9 events/100 patient-years (E/100 PY), and treatment-emergent adverse events (TEAEs) leading to discontinuation, at 1.7 vs 2.7 E/100 PY, compared with Week 16. At Week 304, 86.0% of patients achieved Psoriasis Area and Severity Index (PASI) 90, 54.2% achieved PASI 100, 84.7% attained static Physician’s Global Assessment (sPGA) 0/1, and 76.3% achieved Dermatology Life Quality Index (DLQI) 0/1. 

Key learning: Risankizumab was well tolerated and showed high efficacy through 6 years of continuous treatment in patients with moderate-to-severe plaque psoriasis. The findings suggest risankizumab has the potential to improve outcomes in patients requiring long-term psoriasis management.

References

Please indicate your level of agreement with the following statements:

The content was clear and easy to understand

The content addressed the learning objectives

The content was relevant to my practice

I will change my clinical practice as a result of this content