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A Study to Evaluate the Safety of Remsima® SC in the Treatment of RA, AS, PsA and Ps

Rheumatoid Arthritis Clinical Trial

Official title:
An Observational, Prospective Cohort Study to Evaluate Safety of Remsima® Subcutaneous in Patients With Rheumatoid Arthritis, Ankylosing Spondylitis, Psoriatic Arthritis and Psoriasis

Clinical Trial Summary

This is an observational, prospective cohort study to evaluate the safety of Remsima® SC in the treatment of RA, AS, PsA and Ps.

Clinical Trial Description

CT-P13(Remsima®) is an IgG1 chimeric human-murine mAb biosimilar to Remicade® (infliximab, Janssen Biologics B.V.) developed by CELLTRION, Inc.The purpose of this study is to assess the safety of Remsima® Subcutaneous (SC) in Rheumatoid Arthritis (RA), Ankylosing Spondylitis (AS), Psoriatic Arthritis (PsA) and Psoriasis (Ps) patients by evaluation of adverse events of special interest (AESI) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05866614
Study type Observational [Patient Registry]
Source Celltrion
Contact YounJeong Choi
Phone +82 032 850 5767
Email younjeong.choi@celltrion.com
Status Recruiting
Phase
Start date January 13, 2023
Completion date March 2027
View Details
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