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Continuation Study of Zasocitinib in Adults With Psoriatic Arthritis

Sponsored by Takeda

About this trial

Last updated 17 days ago

Study ID

TAK-279-PsA-3003

Status

Recruiting

Type

Interventional

Phase

Phase 3

Placebo

No

Accepting

18-75 Years
18+ Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Started 25 days ago

What is this trial about?

Psoriatic arthritis (PsA) is a long-term inflammatory disease that affects the joints and skin. The purpose of this study is to check how safe zasocitinib is, how well it is tolerated and how well it works in adults with PsA over a longer period of time. Adults who completed the 1-year (52-week) treatment period in one of the parent studies (TAK-279-PsA-3001 [NCT06671483] or TAK-279-PsA-3002 [NCT06671496]) may be able to join this continuation study (also called long-term extension or LTE study). All participants in this continuation study, will receive zasocitinib (lower or higher dose), once a day (QD). Each participant can be in this study for approximately 2 years (108 weeks). This includes a treatment period of up to 2 years (104 weeks) and a 1-month (4-week) follow-up period to monitor a participant's health.

What are the participation requirements?

Yes

Inclusion Criteria

Men and women aged 18 years or older can participate.
Must have a diagnosis of psoriatic arthritis (PsA).
Must have completed 52-week treatment period in one of the parent studies (TAK-279-PsA-3001 [NCT06671483] or TAK-279-PsA-3002 [NCT06671496]).
The study doctor must believe that the continued or newly started treatment with zasocitinib may help the participant.

Additional entry criteria will be discussed with the study doctor.

Locations

Location

Status

Recruiting

For more information, view the full study details:

NCT07286058