Real-World check: arthritis drug xeljanz XR under safety watch in korea

NCT ID NCT04876781

First seen Nov 01, 2025 · Last updated May 21, 2026 · Updated 32 times

Summary

This study is a post-marketing surveillance required by Korean regulators to monitor the safety and effectiveness of Xeljanz XR (tofacitinib) in everyday medical practice. It will enroll about 200 adults with moderate to severe rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis who are already prescribed the drug. Researchers will track side effects and disease activity scores over roughly four years. The goal is to confirm the drug's real-world safety profile and how well it controls arthritis symptoms.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for ACTIVE MODERATE TO SEVERE RHEUMATOID ARTHRITIS are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Pfizer

    RECRUITING

    Seoul, South Korea

Conditions

Explore the condition pages connected to this study.