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TAK-279-PsA-3001
Recruiting

A Study of Zasocitinib in Adults With Psoriatic Arthritis Who Have Not Taken Biologic Medicines

Clinicaltrials.gov
#NCT06671483
|

About this clinical trial

Psoriatic arthritis (PsA) is a chronic inflammatory disease that affects the joints and skin in people who have psoriasis (PsO). The main aim of the study is to know how well zasocitinib (TAK-279) works in participants with active PsA who have not previously been treated with biologic disease-modifying antirheumatic drugs. The participants will be treated with either zasocitinib, active comparator, or placebo. Participants will be in the study for up to 60 weeks.

US
PL
MX
18+
Interventional Phase 3 clinical trial.

At a glance

What medical conditions are being studied?

Psoriatic Arthritis

What is the clinical trial testing?

Placebo, Zasocitinib, Active Comparator

How many participants are being enrolled?

1088

Are placebos part of the clinical trial?

Yes

When is the clinical trial being conducted?

Mar 2025 - Jan 2028

How long is participation in the clinical trial?

Participants will be in this study for up to 60 weeks.

Key requirements

Sexes

All

Age

18+ Years

Healthy volunteers?

No

Entry criteria

Must be men and women of 18 years or older.
Must have had signs and symptoms of psoriatic arthritis (PsA) for at least 3 months.
Must have active arthritis (at least 3 tender and swollen joints) at the start of the study.
Must have at least 1 symptom of raised and thickened areas of skin known as plaques, or any changes in the appearance of nails.
Did not respond well to at least one of the other treatments for PsA, which includes medicines for inflammation.
Cannot have other conditions that might affect study results (including skin conditions such as rheumatoid arthritis, systemic lupus erythematosus, Lyme disease).
Cannot have previously taken a biologic medicine (made by cells) that is used for treatment of PsA or psoriasis.
Cannot have had a recent infection or have a history of certain infections or medical conditions that might make it hard for them to take part safely in the study.
Additional entry criteria will be discussed by the study doctor.

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