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Japan Post-Marketing Surveillance for Peficitinib to Assess Safety and Effectiveness in the Patients With Rheumatoid Arthritis

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Overview

The objective of this study is to investigate the safety and effectiveness in routine clinical practice and actual clinical setting for all patients with rheumatoid arthritis (RA) treated with peficitinib.

Description

This is a mandatory Post-Marketing Surveillance (PMS) requested by Pharmaceuticals and Medical Devices Agency (PMDA) as a part of the Japan-Risk Management Plan (J-RMP).

Eligibility

Inclusion Criteria:

  • All patients with rheumatoid arthritis (RA) treated with peficitinib for the first time.

Exclusion Criteria:

  • Not applicable.

Study details

Rheumatoid Arthritis (RA)

NCT03971253

Astellas Pharma Inc

22 April 2025

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