Mostrar el registro sencillo del ítem
dc.contributor.author | Suh, Chang-Hee | |
dc.contributor.author | Yoo, Dae Hyun | |
dc.contributor.author | Berrocal Kasay, Alfredo | |
dc.contributor.author | Chalouhi El-Khouri, Elia | |
dc.contributor.author | Cons Molina, Francisco Fidenci | |
dc.contributor.author | Shesternya, Pavel | |
dc.contributor.author | Miranda, Pedro | |
dc.contributor.author | Medina-Rodriguez, Francisco G. | |
dc.contributor.author | Wiland, Piotr | |
dc.contributor.author | Jeka, Slawomir | |
dc.contributor.author | Chavez-Corrales, Jose | |
dc.contributor.author | Linde, Thomas | |
dc.contributor.author | Hrycaj, Pawel | |
dc.contributor.author | Abello-Banfi, Mauricio | |
dc.contributor.author | Hospodarskyy, Ihor | |
dc.contributor.author | Jaworski, Janusz | |
dc.contributor.author | Piotrowski, Mariusz | |
dc.contributor.author | Brzosko, Marek | |
dc.contributor.author | Krogulec, Marek | |
dc.contributor.author | Shevchuk, Sergii | |
dc.contributor.author | Calvo, Armando | |
dc.contributor.author | Andersone, Daina | |
dc.contributor.author | Park, Won | |
dc.contributor.author | Shim, Seung Cheol | |
dc.contributor.author | Lee, Sang Joon | |
dc.contributor.author | Lee, Sung Young | |
dc.date.accessioned | 2019-07-04T17:00:18Z | |
dc.date.available | 2019-07-04T17:00:18Z | |
dc.date.issued | 2019 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12866/6850 | |
dc.description.abstract | Objective: The aim of this study was to investigate long-term clinical outcomes of extended treatment with CT-P10, a rituximab biosimilar, compared with rituximab reference products sourced from the USA and the EU (US-RTX and EU-RTX) in rheumatoid arthritis (RA) for up to 48 weeks. Methods: In this multinational, randomized, double-blind trial, adults with active RA received up to two courses of CT-P10, US-RTX, or EU-RTX alongside methotrexate. Efficacy endpoints included Disease Activity Score 28-joint count (DAS28) and American College of Rheumatology (ACR) response rates. Pharmacokinetics, pharmacodynamics, immunogenicity, and safety were also assessed. Results: Of 372 patients randomized to the study drug, 330 (88.7%) completed the second treatment course. Mean change from baseline to week 48 in DAS28-C-reactive protein was comparable in the CT-P10 and combined rituximab (US-RTX and EU-RTX) groups (− 2.7 and − 2.6, respectively). ACR20, ACR50, and ACR70 response rates at week 48 indicated no differences between groups (80.6%, 55.4%, and 31.7% vs. 79.8%, 53.9%, and 33.7% in the CT-P10 and combined rituximab groups, respectively). Similar improvements in the Health Assessment Questionnaire Disability Index and all medical outcomes in the Short Form 36-Item Health Survey, including physical and mental health, were seen in all groups. At week 48, antidrug antibodies were detected in 4.9%, 9.4%, and 8.6% of patients in the CT-P10, US-RTX, and EU-RTX groups, respectively. CT-P10 and rituximab displayed similar pharmacokinetic, pharmacodynamic, and safety profiles. Conclusion: CT-P10 was similar to EU-RTX and US-RTX in terms of efficacy, pharmacokinetics, pharmacodynamics, immunogenicity, and safety up to week 48. | en_US |
dc.language.iso | eng | |
dc.publisher | Springer | |
dc.relation.ispartofseries | BioDrugs | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es | |
dc.subject | mental health | en_US |
dc.subject | human | en_US |
dc.subject | adult | en_US |
dc.subject | aged | en_US |
dc.subject | female | en_US |
dc.subject | male | en_US |
dc.subject | Article | en_US |
dc.subject | priority journal | en_US |
dc.subject | controlled study | en_US |
dc.subject | major clinical study | en_US |
dc.subject | death | en_US |
dc.subject | drug efficacy | en_US |
dc.subject | multicenter study | en_US |
dc.subject | drug safety | en_US |
dc.subject | drug withdrawal | en_US |
dc.subject | randomized controlled trial | en_US |
dc.subject | lower respiratory tract infection | en_US |
dc.subject | urinary tract infection | en_US |
dc.subject | malignant neoplasm | en_US |
dc.subject | C reactive protein | en_US |
dc.subject | clinical outcome | en_US |
dc.subject | pharmacodynamics | en_US |
dc.subject | methotrexate | en_US |
dc.subject | long term care | en_US |
dc.subject | rheumatoid arthritis | en_US |
dc.subject | antibody detection | en_US |
dc.subject | upper respiratory tract infection | en_US |
dc.subject | treatment duration | en_US |
dc.subject | double blind procedure | en_US |
dc.subject | immunogenicity | en_US |
dc.subject | phase 3 clinical trial | en_US |
dc.subject | rituximab | en_US |
dc.subject | Short Form 36 | en_US |
dc.subject | DAS28 | en_US |
dc.subject | drug antibody | en_US |
dc.subject | infusion related reaction | en_US |
dc.subject | rhinitis | en_US |
dc.title | Long-Term Efficacy and Safety of Biosimilar CT-P10 Versus Innovator Rituximab in Rheumatoid Arthritis: 48-Week Results from a Randomized Phase III Trial | en_US |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | https://doi.org/10.1007/s40259-018-00331-4 | |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.01.05 | |
dc.relation.issn | 1179-190X |
Ficheros | Tamaño | Formato | Ver |
---|---|---|---|
No hay ficheros asociados a este ítem. |