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Assessment of the long-term safety of mepolizumab and durability of clinical response in patients with severe eosinophilic asthma
Indexado
WoS WOS:000466784600010
Scopus SCOPUS_ID:85057186016
DOI 10.1016/J.JACI.2018.09.033
Año 2019
Tipo artículo de investigación

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



Conclusion: These data support the long-term safety and efficacy of mepolizumab in patients with SEA.

Métricas Externas



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Disciplinas de Investigación



WOS
Immunology
Allergy
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Khatri, Sumita Mujer Cleveland Clin Fdn - Estados Unidos
Cleveland Clinic Foundation - Estados Unidos
2 Moore, Wendy Mujer Wake Forest Sch Med - Estados Unidos
Wake Forest School of Medicine - Estados Unidos
Wake Forest University School of Medicine - Estados Unidos
3 Gibson, Peter G. Hombre UNIV NEWCASTLE - Australia
University of Newcastle, Australia - Australia
The University of Newcastle, Australia - Australia
4 Leigh, Richard Hombre Univ Calgary - Canadá
University of Calgary - Canadá
Cumming School of Medicine - Canadá
5 Bourdin, Arnaud Hombre Univ Montpellier - Francia
CHU Montpellier - Francia
Physiologie et Médecine Expérimentale du Cœur et des Muscles - Francia
Hopital Arnaud de Villeneuve - Francia
6 Maspero, Jorge Hombre Fdn Cidea Allergy & Resp Res Unit - Argentina
Fundación Cidea Allergy and Respiratory Research Unit - Argentina
7 Barros, M. Hombre Universidad de Valparaíso - Chile
Hospital Carlos Van Buren - Chile
Hosp Carlos Van Buren - Chile
8 Buhl, R. Hombre Mainz Univ Hosp - Alemania
Klinikum der Johannes-Gutenberg-Universität und Fachbereich Medizin - Alemania
Universitätsmedizin Mainz - Alemania
9 Howarth, Peter Hombre Univ Southampton - Reino Unido
Southampton Gen Hosp - Reino Unido
GSK House - Reino Unido
University of Southampton, Faculty of Medicine - Reino Unido
GlaxoSmithKline plc. - Reino Unido
10 Albers, Frank C. Hombre GSK - Estados Unidos
GlaxoSmithKline, USA - Estados Unidos
GlaxoSmithKline plc. - Estados Unidos
11 Bradford, Eric S. Hombre GSK - Estados Unidos
GlaxoSmithKline, USA - Estados Unidos
GlaxoSmithKline plc. - Estados Unidos
12 Gilson, Martyn Hombre GSK - Reino Unido
GlaxoSmithKline plc. - Reino Unido
13 Price, Robert G. Hombre GSK - Reino Unido
GlaxoSmithKline plc. - Reino Unido
14 Yancey, Steven W. Hombre GSK - Estados Unidos
GlaxoSmithKline, USA - Estados Unidos
GlaxoSmithKline plc. - Estados Unidos
15 Ortega, Hector Hombre GSK - Estados Unidos
GlaxoSmithKline, USA - Estados Unidos
GlaxoSmithKline plc. - Estados Unidos

Muestra la afiliación y género (detectado) para los co-autores de la publicación.

Financiamiento



Fuente
National Institutes of Health
Novartis
National Heart, Lung, and Blood Institute
GlaxoSmithKline
National Health and Medical Research Council
Sanofi
Regeneron Pharmaceuticals
AstraZeneca
Meso Scale Diagnostics
Boehringer Ingelheim
MedImmune
GlaxoSmithKline (GSK)
North Carolina GlaxoSmithKline Foundation
Sanofi Aventis
Roche
Chiesi Farmaceutici
Teva Pharmaceutical Industries
Sanofi Regeneron
Pearl Therapeutics

Muestra la fuente de financiamiento declarada en la publicación.

Agradecimientos



Agradecimiento
This study was funded by GlaxoSmithKline (GSK ID: MEA115666; ClinicalTrials.gov number: NCT01691859).
Disclosure of potential conflict of interest: S. Khatri reports being an investigator in clinical trials in relation to GlaxoSmithKline and Boston Scientific, for which her institution is compensated for time related to the study. W. Moore reports receiving research grants from GlaxoSmithKline, AstraZeneca, Boehringer Ingelheim, Novartis, Pearl Therapeutics, Sanofi Regeneron, and the National Institutes of Health (NIH)/National Heart, Lung, and Blood Institute (NHLBI), and has been an advisory board consultant for AstraZeneca and Sanofi Regeneron. P. G. Gibson reports receiving personal fees from AstraZeneca, GlaxoSmithKline, and Novartis and a research grant from GlaxoSmithKline and the National Health and Medical Research Council (NHMRC). R. Leigh reports receiving honoraria and speakers’ fees from AstraZeneca, Boehringer Ingelheim, GlaxoSmithKline, Novartis, and TEVA; his institution has also received research funding from AstraZeneca, GlaxoSmithKline, MedImmune, Novartis, and Sanofi for clinical trials in which he was a site investigator. A. Bourdin reports receiving personal fees, research grants, and nonfinancial support from GlaxoSmithKline; personal fees and nonfinancial support from AstraZeneca and Novartis; research grants from MSD; research grants and personal fees from Actelion; and personal fees and nonfinancial support from Chiesi. J. Maspero reports attending focus groups and boards for AstraZeneca and receiving personal fees from Novartis, AstraZeneca, GlaxoSmithKline, Sanofi, and Uriach. M. Barros reports receiving honoraria from Boehringer Ingelheim and Grifols for lectures and Advisory boards and has been involved as Principal Investigator in clinical trials for GlaxoSmithKline, Pearl Therapeutics, Sanofi Aventis, and Chiesi. R. Buhl reports personal fees from AstraZeneca, Chiesi, Teva, and Cipla; grants and personal fees from Boehringer Ingelheim, Novartis, and Roche; and grants from GlaxoSmithKline, all of which are outside the submitted work. P. Howarth, F. C. Albers, E. S. Bradford, M. Gilson, R. G. Price, and S. W. Yancy are all employees of GlaxoSmithKline and hold stocks/shares in GlaxoSmithKline. H. Ortega is a former employee of GlaxoSmithKline and holds stocks/shares in GlaxoSmithKline.

Muestra la fuente de financiamiento declarada en la publicación.