dc.contributor | Buitrago Bejarano, Roberto José | |
dc.contributor | Benavides Solarte, Mario | |
dc.creator | Guiot Riveros, Vivian Gissell | |
dc.creator | Giraldo Quintero, Sebastian | |
dc.date.accessioned | 2021-07-01T21:45:21Z | |
dc.date.accessioned | 2022-09-22T13:46:53Z | |
dc.date.available | 2021-07-01T21:45:21Z | |
dc.date.available | 2022-09-22T13:46:53Z | |
dc.date.created | 2021-07-01T21:45:21Z | |
dc.identifier | https://repository.urosario.edu.co/handle/10336/31763 | |
dc.identifier | https://doi.org/10.48713/10336_31763 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/3432441 | |
dc.description.abstract | Introduction: There is no scientific evidence of comparative studies between biosimilars that demonstrate safety and efficacy, this being relevant for clinicians and insurers to feel supported at the time of acquiring and prescribing this type of molecules. In Colombia, since it is a disease with late diagnosis and that consequently presents a greater risk of severity and complication, contemplating a broader portfolio that guarantees the safety profile, quality, and adequate response to treatment would generate a positive impact on access to this type of therapies. Objectives: To determine whether or not there are differences in efficacy according to control of rheumatoid arthritis activity and safety associated with treatment with Biosimilar ABP 501 (Adalimumab), Biosimilar CT-P13 (Infliximab). Methodology: A systematic review of the literature was carried out that included intervention studies, evaluating the clinical responses according to the ACR20, ACR50, ACR 70, DAS 28 PCR, and safety scales evaluated by the formation of anti-drug antibodies and the presence of any adverse events. Results: For ABP 501 80% of the studied population reached an ACR 20 response, 49% for ACR 50 and 26% for ACR 70 at week 24, for CT-P13 71% of the studied population reached an ACR 20 response , 41% ACR 50 and 20% ACR 70 for week 30, while at week 54 and 102 an ACR 20, ACR 50, ACR70 response of 72%, 42% and 33% was evidenced. And 71.7%, 48% and 24.3% respectively. Anti-drug antibodies ABP 502 Week 24 of 38.3%, week 52 54%. CT-P13, week 30, 54, 102 of 40%, 41% and 41% respectively. Discussion: ABP 501 and CT-P13 showed safety and effectiveness in patients with moderate to severe RA, showing a superior clinical response in those patients treated with ABP 501, in long-term safety CT-P13 presented greater safety by presenting a lower proportion of patients with anti-drug antibodies. | |
dc.language | spa | |
dc.publisher | Universidad del Rosario | |
dc.publisher | Maestría en Epidemiología | |
dc.publisher | Escuela de Medicina y Ciencias de la Salud | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/2.5/co/ | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.rights | Abierto (Texto Completo) | |
dc.rights | EL AUTOR, manifiesta que la obra objeto de la presente autorización es original y la realizó sin violar o usurpar derechos de autor de terceros, por lo tanto la obra es de exclusiva autoría y tiene la titularidad sobre la misma.
PARGRAFO: En caso de presentarse cualquier reclamación o acción por parte de un tercero en cuanto a los derechos de autor sobre la obra en cuestión, EL AUTOR, asumirá toda la responsabilidad, y saldrá en defensa de los derechos aquí autorizados; para todos los efectos la universidad actúa como un tercero de buena fe.
EL AUTOR, autoriza a LA UNIVERSIDAD DEL ROSARIO, para que en los términos establecidos en la Ley 23 de 1982, Ley 44 de 1993, Decisión andina 351 de 1993, Decreto 460 de 1995 y demás normas generales sobre la materia, utilice y use la obra objeto de la presente autorización.
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POLITICA DE TRATAMIENTO DE DATOS PERSONALES. Declaro que autorizo previa y de forma informada el tratamiento de mis datos personales por parte de LA UNIVERSIDAD DEL ROSARIO para fines académicos y en aplicación de convenios con terceros o servicios conexos con actividades propias de la academia, con estricto cumplimiento de los principios de ley. Para el correcto ejercicio de mi derecho de habeas data cuento con la cuenta de correo habeasdata@urosario.edu.co, donde previa identificación podré solicitar la consulta, corrección y supresión de mis datos. | |
dc.rights | Atribución-NoComercial-SinDerivadas 2.5 Colombia | |
dc.rights | Atribución-NoComercial-SinDerivadas 2.5 Colombia | |
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dc.source | Instituto Nacional de medicamentos y alimentos INVIMA (2015) INFORME DE ANÁLISIS DE EVENTOS ADVERSOS SERIOS NACIONALES EN ENSAYOS CLÍNICOS CON MEDICAMENTOS REPORTADOS EN EL AÑO 2015. Disponible en: https://www.invima.gov.co/documents/20143/790891/2015Informe+EASa+2015.pdf/dbb641ef-616e-661d-ecf4-0b77fa9c863e. | |
dc.source | instname:Universidad del Rosario | |
dc.source | reponame:Repositorio Institucional EdocUR | |
dc.subject | Uso de biosimilares ABP 501 y CT-P13 en enteramiento de Artritis reumatoide | |
dc.subject | Analisis de seguridad en el uso de Infliximab (anticuerpo monoclonal quimérico) | |
dc.subject | Análisis de uso seguro de Amgevita® | |
dc.subject | Análisis de uso seguro de Remsina® | |
dc.subject | Análisis de eficacia y seguridad del uso de fármacos de tratamiento biológico | |
dc.subject | Uso de biosimilares ABP 501 (Adalimumab) y CT-P13 (Infliximab) en el tratamiento de Artritis reumatoide | |
dc.title | Eficacia y seguridad del biosimilar ABP 501 (Adalimumab) comparado con biosimilar CT-P13 (Infliximab) en pacientes adultos con artritis reumatoide. Revisión sistemática | |
dc.type | masterThesis | |