86 0

Full metadata record

DC FieldValueLanguage
dc.contributor.author유대현-
dc.date.accessioned2022-01-14T04:48:03Z-
dc.date.available2022-01-14T04:48:03Z-
dc.date.issued2020-06-
dc.identifier.citationCLINICAL DRUG INVESTIGATION, v. 40, no. 6, page. 541-553en_US
dc.identifier.issn1173-2563-
dc.identifier.issn1179-1918-
dc.identifier.urihttps://link.springer.com/article/10.1007%2Fs40261-020-00907-5-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/167131-
dc.description.abstractBackground The infliximab biosimilar CT-P13 has widely received regulatory approval in all indications of reference infliximab, including rheumatoid arthritis (RA) and ankylosing spondylitis (AS). Objective This retrospective analysis investigated drug survival and long-term safety and effectiveness of CT-P13 in patients with RA or AS in the Republic of Korea. Methods This non-interventional, retrospective, multicenter analysis collected medical record data for adult patients with RA or AS who received CT-P13 treatment at five Korean referral hospitals (2012-2017). Drug survival and long-term safety were primary outcomes. The secondary outcome was long-term effectiveness, assessed by disease activity measures. Results Overall, 491 patients were treated with CT-P13 (154 patients with RA [135 infliximab-naive; 19 switched from reference infliximab]; 337 patients with AS [219 infliximab-naive; 118 switched from reference infliximab]). Drug survival was similar in naive and switched patients. Treatment-emergent adverse events (TEAEs) occurred in 31.8% and 29.4% of patients with RA and AS, respectively; incidence was similar in naive and switched groups. Upper respiratory tract infection, influenza-like illness, and urticaria were the most common TEAEs. Overall, nine (1.8%) patients experienced serious adverse events (SAEs) deemed potentially drug-related; SAEs led to permanent CT-P13 discontinuation in five (1.0%) patients, including three with tuberculosis. Disease activity decreased over time. Conclusion Up to 5 years of CT-P13 treatment was safe and effective in patients with RA and AS, based on drug survival, incidence of TEAEs, and disease activity. Drug survival and safety were similar in naive patients and switched groups, supporting switching from reference infliximab to CT-P13.en_US
dc.description.sponsorshipThis study was supported by Celltrion Healthcare Co., Ltd. (Incheon, Republic of Korea).en_US
dc.language.isoenen_US
dc.publisherADIS INT LTDen_US
dc.subjectNECROSIS-FACTOR INHIBITORSen_US
dc.subjectMODIFYING ANTIRHEUMATIC DRUGSen_US
dc.subjectLONG-TERM SAFETYen_US
dc.subjectRETENTION RATEen_US
dc.subjectINNOVATOR INFLIXIMABen_US
dc.subjectPARALLEL-GROUPen_US
dc.subjectDOUBLE-BLINDen_US
dc.subjectREAL-WORLDen_US
dc.subjectEFFICACYen_US
dc.subjectVASCULITISen_US
dc.titleA 5-year Retrospective Analysis of Drug Survival, Safety, and Effectiveness of the Infliximab Biosimilar CT-P13 in Patients with Rheumatoid Arthritis and Ankylosing Spondylitisen_US
dc.typeArticleen_US
dc.relation.no6-
dc.relation.volume40-
dc.identifier.doi10.1007/s40261-020-00907-5-
dc.relation.page541-553-
dc.relation.journalCLINICAL DRUG INVESTIGATION-
dc.contributor.googleauthorKim, Tae-Hwan-
dc.contributor.googleauthorLee, Shin-Seok-
dc.contributor.googleauthorPark, Won-
dc.contributor.googleauthorSong, Yeong Wook-
dc.contributor.googleauthorSuh, Chang-Hee-
dc.contributor.googleauthorKim, SooKyoung-
dc.contributor.googleauthorLee, Young Nam-
dc.contributor.googleauthorYoo, Dae Hyun-
dc.relation.code2020050740-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.piddhyoo-
dc.identifier.researcherIDM-3924-2017-
Appears in Collections:
COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML


qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE