A study to describe the one-year persistence in participants treated by Flixabi (infliximab) or Imraldi (Adalimumab) as prescribed by the physician for each of the 5 following indications: Rheumatoid Arthritis (RA), Ankylosing Spondylitis (AS), Psoriatic Arthritis (PsA), Crohn's Disease (CD) \[adults and children\] and Ulcerative Colitis (UC) \[adults for both treatments and children only for Flixabi\].
Study Type
OBSERVATIONAL
Enrollment
2,274
Administered as specified in the treatment arm.
Administered as specified in the treatment arm.
Research Site
Caluire-et-Cuire, Auvergne-Rhône-Alpes, France
Research Site 1
Clermont-Ferrand, Auvergne-Rhône-Alpes, France
Research Site
Clermont-Ferrand, Auvergne-Rhône-Alpes, France
Research Site
Lyon, Auvergne-Rhône-Alpes, France
Research Site 1
Pierre-Bénite, Auvergne-Rhône-Alpes, France
Percentage of Participants who are Still Treated with Either Flixabi or Imraldi at 12 Months
Percentage of participants, either infliximab naïve or switched from Remicade or CT-P13 to Flixabi, who are still treated with Flixabi, and either adalimumab naïve or switched from Humira or other adalimumab biosimilars to Imraldi, who are still treated with Imraldi, at 12 months for RA, AS, PsA, CD (adults and children), and UC (adults for both treatments and children only for Flixabi) will be reported.
Time frame: Up to 12 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Research Site
Pierre-Bénite, Auvergne-Rhône-Alpes, France
Research Site
Saint-Etienne, Auvergne-Rhône-Alpes, France
Research Site
Dijon, Bourgogne-Franche-Comté, France
Research Site 1
Brest, Brittany Region, France
Research Site
Brest, Brittany Region, France
...and 50 more locations