Continuation Study of Zasocitinib in Adults With Psoriatic Arthritis
Takeda · NCT07286058
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 3
- Target enrollment
- 1182
- US sites recruiting
- 19
- Study start
- March 11, 2026
- Record last updated
- September 9, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is 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.
Being studied: Zasocitinib
Conditions: Psoriatic Arthritis
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- 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 Criteria
- 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).
- 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.
- 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).
Recruiting US locations
Jeffrey Loomer, MD Arizona Arthritis & Rheumatology Research
Tucson, AZ 85748
Site contact: Site Contact · 85748 · loomer.research@azarthritis.com
First OC Dermatology Research Inc.
Fountain Valley, CA 92708
Site contact: Site Contact · 714-531-2966 · vivian.laquer@firstocdermresearch.com
Purushotham & Akther Kotha MD
La Mesa, CA 91942
Site contact: Site Contact · roshankotha@gmail.com
Triwest Research Associates LLC
La Mesa, CA 91942
Site contact: Site Contact · 619-334-4735 · drmabaquiao@triwestresearch.com
The Cohen Medical Centers
Thousand Oaks, CA 91360-3967
Site contact: Site Contact · 805-904-0982 · drcohen@wmresearch.com
Denver Arthritis Clinic - Lowry
Denver, CO 80230
Site contact: Site Contact · rantolini@dacdenver.com
Direct Helpers Research Center
Hialeah, FL 33012
Site contact: Site Contact · 305-828-3555 · don@dhrtrials.com
Sweet Hope Research Specialty, Inc, d/b/a Neoclinical Research
Hialeah, FL 33016
Site contact: Site Contact · csesin1979@aol.com
IRIS Research and Development
Plantation, FL 33324
Site contact: Site Contact · 954-476-2338 · drvalenzuela@irisrheumatology.com
Klein and Associates, M.D., P.A.
Hagerstown, MD 21740-6138
Site contact: Site Contact · 301-791-6680 · ookoye@rheumdocs.com
Paramount Medical Research & Consulting, LLC
Middleburg Heights, OH 44130
Site contact: Site Contact · 440-826-0742 · idiabmd@gmail.com
West Tennessee Research Institute
Jackson, TN 38305
Site contact: Site Contact · 731-633-0145 · aresearch@arthritisclinic.org
Accurate Clinical Research
Baytown, TX 77521
Site contact: Site Contact · 832-705-7839 · snajammd@accurateclinicalresearch.com
Novel Research LLC
Bellaire, TX 77401
Site contact: Site Contact · 832-400-2262 · wajeeha@novelresearch.net
Novel Research | Abigail Neiman - Houston, TX
Houston, TX 77024
Site contact: Site Contact · neiman@novelresearch.net
Northwest Houston Arthritis Center
Houston, TX 77090
Site contact: Site Contact · 832-834-5627 · adnan@novelresearch.net
West Texas Clinical Research
Lubbock, TX 79424
Site contact: Site Contact · 806-993-1040 · jitendra.vasandani@yahoo.com
Southwest Rheumatology Research, LLC
Mesquite, TX 75150
Site contact: Site Contact · 972-288-2600 · asinghal@swrr.net
Advanced Rheumatology of Houston
The Woodlands, TX 77382united
Site contact: Site Contact · 281-766-7886 · tbrionez@gmail.com
Study contacts (from the official record)
- Takeda Contact · +1-877-825-3327 · medinfoUS@takeda.com
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