Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Pfizer
Non-interventional study: subjects to be selected according to the usual clinical practice of their physician
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subject eligibility should be reviewed and documented by an appropriately qualified member of the investigator's study team before subjects are included in the study.
Evidence of a personally signed and dated informed consent document indicating that the subject (or a legally acceptable representative) has been informed of all pertinent aspects of the study is a requirement for inclusion into this study.
Subjects who are willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
Definitive diagnosis of RA or PsA.
Eligible for Etanercept treatment according to Summary of Product Characteristics (SmPC).
Inclusion of subjects pretreated with other biologics other than Etanercept is possible
One plain radiograph of hands and feet (Anteroposterior) within 3 month prior to initiation of treatment with Etanercept and one planned consecutive radiograph of hand and feet taken over 12 to 18 months according to German recommendations for patients treated with biologics.
You may not be if
Receipt of any investigational drug within 3 months of study inclusion.
Hypersensitivity to the active substance (etanercept) or to any of the excipients.
Sepsis or risk of sepsis.
Active infections, including chronic or localised infections.
Subjects who have received any previous treatment with etanercept
Subjects who are investigational site staff members or subjects who are Pfizer employees directly involved in the conduct of the trial.
