Effectiveness of Treatment With Tofacitinib in Patients With Psoriatic Arthritis in Routine Clinical Practice
About the study
This is a Multinational Study of Tofacitinib in Patients Treated for Psoriatic Arthritis in order to evaluate the effectiveness of treatment with tofacitinib on disease activity, remission, and Quality of Life, in a real-world setting over a 12-month observation period
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria: Patients must meet all of the following inclusion criteria to be eligible for inclusion in the study:
- Patients aged ≥ 18 years
- Moderate to severe PsA disease activity diagnosed
- Patients for whom the physician's decision has been made to initiate treatment with tofacitinib, in usual clinical practice conditions and in compliance with the local label
- Patients are treatment naïve to tofacitinib on the date of providing informed consent
- Evidence of a personally signed and dated informed consent document indicating that the patient (or a legally acceptable representative) has been informed of all pertinent aspects of the study
- Patients on DMARDs must have not had a treatment change in the past 3 months
EXCLUSION CRITERIA
Exclusion Criteria: Patients meeting any of the following criteria will not be included in the study:
- Contraindications according to the Xeljanz® (tofacitinib) Prescribing Information
- Receipt of any investigational drug within 3 months before study inclusion
- Patient is pregnant or breastfeeding
- Recent herpes zoster infection (within past 6 months) or history of severe disseminated herpes zoster infection
- Active treatment for a malignancy
- Concomitant treatment with a biological disease-modifying antirheumatic drugs (bDMARD)
Study Locations
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How to Apply
Contact the study center to learn if this study is a good match for you.
Study’s details
Contition
Psoriatic Arthritis
Age (in years)
18+
Participants needed
500
Est. Completion Date
Jul 22, 2024
Treatment type
Observational [Patient Registry]
Sponsor
Pfizer
ClinicalTrials.gov identifier
NCT04517669
Study number
A3921332
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