Long-term study of zasocitinib for joint and skin psoriatic arthritis
Checks long-term safety of zasocitinib in adults with active psoriatic arthritis.
Plain-language title generated from the registry record
Registry title: Continuation Study of Zasocitinib in Adults With Psoriatic Arthritis
Key facts
- Where
- Bad Bentheim, Bad Doberan, Berlin, Dresden, Hamburg, Herne, Leipzig, Munich, and Ratingen, GermanySee the 10 sites
- Phase
- Phase 3
Where in Germany
- Thermalsole und Schwefelbad Bentheim GmbHBad Bentheim, GermanyTaking people
- Prof. Dr. med. Gunther Neeck MVZ GmbHBad Doberan, GermanyTaking people
- ISA - Interdisciplinary Study Association GmbHBerlin, GermanyTaking people
- Rheumatologische SchwerpunktpraxisBerlin, GermanyTaking people
- Staedtisches Klinikum DresdenDresden, GermanyTaking people
- MVZ Rheumatologie und Autoimmunmedizin Hamburg GmbHHamburg, GermanyTaking people
- St. Elisabeth Gruppe GmbH Katholische Kliniken Rhein-RuhrHerne, GermanyTaking people
- Universitaetsklinikum Leipzig AorLeipzig, GermanyTaking people
- Medicover GmbHMunich, GermanyTaking people
- Studienambulanz Rheumazentrum Ratingen GbRRatingen, GermanyTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Takeda
- Trial code
- NCT07286058EU 2025-522586-30-00
- Record updated
- 9 September 2026
- Original description
Psoriatic arthritis (PsA) is a long-term inflammatory disease that affects the joints and skin.Read full original descriptionShow less
A Phase 3, Multicenter, Long-Term Extension Study to Evaluate the Long-Term Safety, Tolerability, and Efficacy of Zasocitinib (TAK-279) in Subjects With Active Psoriatic Arthritis Who Are Either Biologic DMARD-Naïve or Biologic DMARD-Experienced, Including Those With Inadequate Response to Biologic DMARDs
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.
Inclusion: The participant is aged 18 years or older at the time of signing the informed consent form (ICF). In South Korea, the age requirement for adult participants is >=19 years of age; The participant has completed the 52-week treatment period in one of the parent studies (TAK-279-PsA-3001 or TAK-279-PsA-3002) independent of treatment assignment, and without meeting the criteria for permanent discontinuation of trial intervention defined in the parent studies; The participant must be deemed by the investigator to benefit from continued or newly initiated (that is, for participants randomized to active comparator in parent study TAK-279-PsA-3001) zasocitinib therapy.
Exclusion: The participant has developed evidence of a concomitant comorbid skin condition that, in the opinion of the investigator, would interfere with the study assessments, such as evidence of non-plaque PsO (erythrodermic, pustular, predominately guttate PsO, inverse, or drug-induced PsO); The participant has developed any disease(s) that might confound the evaluations of benefit of zasocitinib therapy since enrollment in the respective parent study, including but not limited to rheumatoid arthritis, axial spondyloarthritis (this does not include a primary diagnosis of PsA with spondylitis), systemic lupus erythematosus, Lyme disease, gout, or fibromyalgia; Any participant who is deemed by the investigator to be not benefiting from the trial intervention based upon lack of improvement or worsening of their symptoms in the respective parent study; Any participant who met the criteria for permanent discontinuation of trial intervention defined in the parent studies (TAK-279-PsA-3001 or TAK-279-PsA-3002).