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Clinical Trial Summary

This is a Phase 3, long-term open-label extension study to evaluate the safety, tolerability and efficacy of tofacitinib in subjects with active PsA who have previously participated in randomized studies of tofacitinib for this indication.

This study will include a sub-study to evaluate the efficacy, safety and tolerability of tofacitinib 5 mg BID administered as monotherapy after methotrexate withdrawal compared to tofacitinib 5 mg BID continued in combination with methotrexate. The sub-study will be available to subjects who have completed at least 24 months of participation in the open-label extension study and meet eligibility criteria for the sub-study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01976364
Study type Interventional
Source Pfizer
Contact
Status Completed
Phase Phase 3
Start date February 17, 2014
Completion date May 20, 2019

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