Mortality risk reduction with budesonide/glycopyrrolate/formoterol fumarate versus fluticasone furoate/umeclidinium/vilanterol in COPD: a matching-adjusted indirect comparison based on ETHOS and IMPACT

Daiana Stolza Clinic of Respiratory Medicine, Medical Center and Faculty of Medicine, University of Freiburg, Freiburg, GermanyCorrespondence[email protected]

Erik Hermanssonb AstraZeneca, Gothenburg, Sweden

Mario Ouwensb AstraZeneca, Gothenburg, Sweden

Barinder Singhc Pharmacoevidence, Mohali, India

Akanksha Sharmac Pharmacoevidence, Mohali, India

Dan Jacksond AstraZeneca, Cambridge, UK

Patrick Darkene AstraZeneca, Gaithersburg, MD, USA

Jonathan Marshalld AstraZeneca, Cambridge, UK

Karin Bowene AstraZeneca, Gaithersburg, MD, USA

Hana Müllerovád AstraZeneca, Cambridge, UK

Bernardino Alcázar Navarretef Respiratory Department, Hospital Universitario Virgen de las Nieves, Granada, Spain;g Instituto Biosanitario de Granada, IBS-Granada, Granada, Spain

Richard Russellh King’s Centre for Lung Health, Department of Immunobiology, School of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King’s College London, London, UK

MeiLan K. Hani Division of Pulmonary and Critical Care, University of Michigan, Ann Arbor, MI, USA

Deniz Tansey-Dwyerd AstraZeneca, Cambridge, UK

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Mortality risk reduction with budesonide/glycopyrrolate/formoterol fumarate versus fluticasone furoate/umeclidinium/vilanterol in COPD: a matching-adjusted indirect comparison based on ETHOS and IMPACT

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Mortality risk reduction with budesonide/glycopyrrolate/formoterol fumarate versus fluticasone furoate/umeclidinium/vilanterol in COPD: a matching-adjusted indirect comparison based on ETHOS and IMPACT

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