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A Study About How Well TAK-279 Works and Its Safety in Participants With Moderate-to-severe Plaque Psoriasis During 52 Weeks of Treatment

About

Brief Summary

The main aim of this study is to show how well TAK-279 reduces the skin plaques compared to placebo, in participants with moderate-to-severe plaque psoriasis. Participants will be assigned to one of the 3 study treatments (TAK-279, apremilast (an approved treatment), or a placebo). Participants will be in the study for up to 61 weeks.

Primary Purpose
Treatment
Study Type
Interventional
Phase
Phase 3

Eligibility

Gender
All
Healthy Volunteers
No
Minimum Age
18 Years
Maximum Age
N/A

Inclusion Criteria:

  • Plaque psoriasis for at least 6 months.
  • Moderate to severe disease.
  • Candidate for phototherapy or systemic therapy.

Exclusion Criteria:

  • Other forms of psoriasis.
  • History of recent infection.
  • Prior exposure to TAK-279 or active comparator.

Other protocol defined inclusion/exclusion criteria apply.

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Study Stats
Protocol No.
23-5201
Category
Autoimmune Disorders
Contact
Ross Divinagracia
Location
  • UCLA Santa Monica
  • UCLA Westwood
For Providers
NCT No.
NCT06088043
For detailed technical eligibility, visit ClinicalTrials.gov.