A Study of Zasocitinib in Adults With Psoriatic Arthritis Who Have Not Taken Biologic Medicines
Sponsored by Takeda
About this study
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.
Where this study is enrolling (46)
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Arizona Arthritis & Rheumatology Research, PLLC | Phoenix, AZ
Phoenix, Arizona
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AARR- Chandler AZ
Chandler, Arizona
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Purushotham & Akther Kotha MD
La Mesa, California
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Triwest Research Associates LLC
La Mesa, California
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The Cohen Medical Centers
Thousand Oaks, California
Show all 46 locations
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First OC Dermatology Research Inc.
Fountain Valley, California
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Foothill Arthritis Clinic
Tujunga, California
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Denver Arthritis Clinic | Denver, CO
Denver, Colorado
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RASF- Clinical Research Center
Boca Raton, Florida
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Arthritis & Rheumatic Disease Specialties (AARDS)
Aventura, Florida
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Bioresearch Partners
Miami, Florida
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Clinical Research of West Florida | Clearwater, FL
Clearwater, Florida
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Clinical Research of West Florida | Tampa, FL
Tampa, Florida
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GNP Research, LLC | Hollywood, FL
Cooper City, Florida
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IRIS Research and Development | Plantation, FL
Plantation, Florida
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Millennium Research | Ormond Beach, FL
Ormond Beach, Florida
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Sarasota Arthritis Research Center
Sarasota, Florida
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Sweet Hope Research Specialty, Inc, d/b/a Neoclinical Research
Hialeah, Florida
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Tectum Medical Research
Davie, Florida
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West Broward Rheumatology Associates, Inc.
Tamarac, Florida
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Marietta Rheumatology Associates
Marietta, Georgia
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Greater Chicago Specialty Physicians LLC/CIS
Schaumburg, Illinois
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GSCP/CIS
Orland Park, Illinois
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Accurate Clinical Research, Inc. | Lake Charles
Lake Charles, Louisiana
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Klein & Associates, M.D., P.A.
Hagerstown, Maryland
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June DO, PC Private Practice - Dr. Justus Fiechtner
Lansing, Michigan
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Clinical Research Institute of Michigan
Saint Clair Shores, Michigan
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Michigan Rheumatology Group, P.C. - Grand Blanc Office
Grand Blanc, Michigan
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Ash Research Clinic - Howell
Howell, Michigan
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Saint Louis Rheumatology
St Louis, Missouri
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Santa Fe Rheumatology
Santa Fe, New Mexico
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Albuquerque Center for Rheumatology PC
Albuquerque, New Mexico
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NYU Langone Health | Joseph S. and Diane H. Steinberg Ambulatory Care Center - Rheumatology Department
Brooklyn, New York
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Accellacare of Hickory
Hickory, North Carolina
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Paramount Medical Research & Consulting, LLC
Middleburg Heights, Ohio
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University Hospitals | UH Cleveland Medical Center - Department of Medicine - Rheumatology Division
Cleveland, Ohio
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PA Regional Center for Arthritis and Osteoporosis Research
Wyomissing, Pennsylvania
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West Tennessee Research Institute
Jackson, Tennessee
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Clinical Investigations of Texas
Plano, Texas
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Southwest Rheumatology Research, LLC | Mesquite, TX
Mesquite, Texas
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Accurate Clinical Research
Baytown, Texas
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Introscience Research | Northwest Houston Arthritis Center - Houston, TX
Houston, Texas
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Novel Research | Bellaire Location
Bellaire, Texas
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Accurate Clinical Research
Houston, Texas
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West Texas Clinical Research
Lubbock, Texas
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Arthritis Northwest, PLLC | Spokane, WA
Spokane, Washington
Who can participate
Inclusion criteria
- ✓1. 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.
- ✓Disease Characteristics:
- ✓2. The participant has a diagnosis of PsA.
- ✓3. The participant must have signs and symptoms of PsA for at least 3 months prior to screening.
- ✓4. The participant meets the Classification Criteria for Psoriatic Arthritis (CASPAR criteria).
- ✓5. The participant has active arthritis as shown by a minimum of \>=3 tender joints in TJC68 and \>=3 swollen joints in SJC66 at the screening and baseline (Day 1) visits.
- ✓6. The participant has at least 1 active lesion of plaque PsO \>=2 cm in diameter, or any nail or nail bed changes characteristic of PsO.
- ✓Medications for PsA:
- ✓7. The participant has had at least one of the following:
- ✓1. Inadequate response to a nonsteroidal anti-inflammatory drug (NSAID) (not applicable in the European Union \[EU\]/ European Economic Area \[EEA\]), OR
- ✓2. Inadequate response to a conventional synthetic disease-modifying antirheumatic drug (csDMARD).
Exclusion criteria
- ✕PsA and PsO:
- ✕1. The participant has other disease(s) that might confound the evaluations of benefit of zasocitinib therapy, including but not limited to rheumatoid arthritis, axial spondyloarthritis, systemic lupus erythematosus, Lyme disease, gout, or fibromyalgia.
- ✕2. The participant has 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).
Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.
Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.