Long Term Evaluation of Safety and Efficacy of Tildrakizumab in Patients With Psoriatic Arthritis

Prior treatment

• Subject has previously been enrolled in this long-term extension study.

Other illness

• Any condition that in the opinion of the Investigator represents an obstacle for study conduct and/or represents a potential unacceptable risk for the subject.

Other

• Female subjects of childbearing potential who do not agree to abstain from heterosexual activity or practice a dual method of contraception.
• Female is pregnant or breastfeeding, or planning to become pregnant or initiate breastfeeding while enrolled in the study or up to 17 weeks after the last dose of IMP.

• Subjects possess the ability to understand the requirements of the study.
• Subject has provided written informed consent as evidenced by signature on an informed consent form approved by an institutional review board/EC.
• Agree to abide by the study restrictions, scheduled treatment, laboratory assessments, other study procedures and return to the site for the required assessments.
• Subject with PsA who had met all eligibility criteria for the parent study, had completed the parent study treatment period and has not developed any parent protocol criteria for premature discontinuation of treatment or withdrawal from the study.