A Study of the Safety and Efficacy of Risankizumab in Adult Participants With Plaque Psoriasis Who Have Had a Suboptimal Response to Secukinumab or Ixekizumab

  • STATUS
    Recruiting
  • End date
    Oct 26, 2022
  • participants needed
    250
  • sponsor
    AbbVie
Updated on 6 October 2021
secukinumab
ixekizumab

Summary

This study will evaluate whether adult participants with moderate to severe plaque psoriasis who have been treated with secukinumab or ixekizumab for at least 6 months and are experiencing a suboptimal response may benefit from switching to risankizumab with regard to skin symptoms, quality of life symptoms and psoriasis symptoms.

Study duration will last for up to 64 weeks with risankizumab given by subcutaneous injection at Week 0, Week 4, and then every 12 weeks for 52 Weeks. An additional visit will occur at Week 8 for a physical exam and questionnaire collection. A final follow-up phone call will occur at Week 60.

Details
Condition Plaque Psoriasis
Treatment risankizumab
Clinical Study IdentifierNCT04102007
SponsorAbbVie
Last Modified on6 October 2021

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