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+ Years
All
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?
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