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Psoriasis Study

The purpose of this study is to determine if an investigational medication taken by mouth, called zasocitinib, is safe and works better than deucravacitinib for patients who have moderate to severe plaque psoriasis.

Age & Gender

  • 18 years ~ 99 years
  • Male, Female, Gender Inclusive

Visit Availability

  • Standard business hours (M-F, 8-5)

Location

North Carolina (Statewide)

What will be asked of you

At each visit, you will meet with a member of the study team and fill out questionnaires. The study also involves vital signs, blood draws, urine testing, physical exams, ECGs, and a Chest x-ray. You must provide a complete medical history and medication use. Women of child bearing potential will be required to use a birth control method approved by the study. Participants must be willing to take the study medication every day during the study.

Incentives

Additional information can be provided upon request

In-person visits:
9
Total length of participation:
20 weeks

Looking for Specific Volunteers

Able to participate:

  • You have a diagnosis of plaque psoriasis
  • You have active psoriasis affecting 10% or more of your skin
  • You are at least 18 years old.

Not eligible if:

  • You have primarily other types of psoriasis other than plaque type.
  • You require treatment for an immune related disease.
  • You have an active infection or a history of certain serious infections.
  • You have uncontrolled or severe high blood pressure.

Contact the Team

Visit Location

Contact & Visit Location

Primary Contact

Primary Visit Location

Dermatology Clinical Trials Unit (DCTU)
UNC Dermatology and Skin Cancer Center at Southern Village
410 Market St Ste 362, Chapel Hill, NC 27516, USA

Additional Study Information

Principal Investigator

Laura Ferris
Dermatology-Research

Study Type

Clinical or Medical
Interventional

Study Topics

Skin, Hair, and Nails

IRB Number

25-0871

ClinicalTrials.gov

not yet available

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