Long Term Clinical Trial Study for Psoriatic Arthritis (PsA), Ankylosing Spondylitis (AS), and Non-Radiographic Axial Spondyloarthritis (nr-axSpA) Patients taking Tildrakizumab

By Spondylitis Association of America

Wednesday, February 27, 2019

The following is an announcement from SAA about a third party clinical trial. SAA is not affiliated with this study, the researchers, or the drug manufacturer.


A phase 2/3 clinical trial is now recruiting patients over the age of 18 with active psoriatic arthritis (PsA), ankylosing spondylitis (AS), or non-radiographic axial spondyloarthritis (nr-axSpA) to participate in a multiple-dose, long-term extension study (4-years). This study is a follow up, and is recruiting those who have previously participated in the parent study involving the medication Tilldrakizumab.

The purpose of the trial titled, “A Long Term Study to Demonstrate the Safety and Efficacy of Tildrakizumab in Subjects With Psoriatic Arthritis and Ankylosing Spondylitis or Non-Radiographic Axial Spondyloarthritis” is to study the safety and efficacy of Tildrakizumab in those with psoriatic arthritis (PsA), ankylosing spondylitis (AS) or non-radiographic axial spondyloarthritis (nr-axSpA).

Study qualifications include:

  • • Age 18-99
  • • Have a clinical diagnosis of psoriatic arthritis (PsA), ankylosing spondylitis (AS) or non-radiographic axial spondyloarthritis (nr-axSpA), and have completed the parent study with baseline improvement of 20% in symptoms.
  • • Not currently on the medications leflunomide and/or methotrexate
  • • No history of active tuberculosis (TB) or symptoms of TB
  • • Ability to provide a 4-year commitment to the study

More information can be found on the Clinical Trials website.

Please visit the clinical trials study locations page for contact information, and to locate specific study locations. You can also contact the study sponsor, Sun Pharma Global FZE, for more information at clinical.trials@sparcmail.com


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