An Open-Label Extension Study to Evaluate Long Term Safety and Efficacy of Tildrakizumab in Patients with Psoriatic Arthritis - NI

Sun Pharmaceutical Industries Limited0 个研究点目标入组 0 人开始时间: 待定最近更新: 2024年8月19日

试验速览

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•1.Subjects possess the ability to understand the requirements of the study.2.Subject has provided written informed consent as evidenced by signature on an informed consent form approved by an institutional review board/EC.3.Agree to abide by the study restrictions, scheduled treatment, laboratory assessments, other study procedures and return to the site for the required assessments.4.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.5.Psoriatic Arthritis subjects who achieved ACR20 response at study entry AND the subject has received sufficient clinical benefit,in the opinion of the Investigator,to support continued treatment with Tildrakizumab.

•1.Female subjects of childbearing potential who do not agree to abstain from heterosexual activity or practice a dual method of contraception.2.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.3.Subject has previously been enrolled in this long-term extension study.4.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.

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