Last updated on 28 February 2025
AvATher is an expert advisory group that provides evidence-based advice on antiviral compounds and monoclonal antibodies targeting Covid-19, as well as other respiratory viruses, in late preclinical or clinical development.
Initially designed to evaluate antiviral drugs against Covid-19, AvATher is extending its scope to other respiratory viruses (Coronavirus, influenza, RSV, other viruses considered to be priority pathogens). The group works with the agency’s other facilitation groups, in particular the Coordinated Action on Respiratory Viruses and the GEPC Preclinical Studies Group.
In the event of an epidemic crisis caused by other pathogens (viral haemorrhagic fever, Arbovirus, etc.), the group may exceptionally be asked to issue opinions and/or recommendations, or to appraise clinical trials concerning new antiviral candidates potentially active against the pathogen.
In particular, the AvATher group is responsible for :
Lionel Piroth
Dijon University Hospital
Laurence Weiss
Paris Cité University
Claire Andrejak
(Amiens University Hospital)
Yvanie Caillé
(Association Renaloo)
Sophie Caillard-Ohlmann
(Strasbourg University Hospitals, Head of department (Nephrology, dialysis and transplantation) )
Xavier de Lamballerie
(Aix-Marseille University)
Alban Dhanani
(ANSM)
Alexandre Dauvignaud
(Bordeaux University Hospital)
Jérémie Guedj
(Inserm)
Julie Helms
(Strasbourg University Hospitals)
Maya Hites
(Erasmus Hospital – Université libre de Bruxelles)
Bruno Hoen
(Lorraine University)
Vincent Levy
(AP-HP)
Robert Manfredi
(French Ministry of Health and Prevention /Population Health Division)
Guillaume Martin-Blondel
(Toulouse University Hospital)
Mathieu Molimard
(Bordeaux University)
Nathan Piffer Smadja
(AP-HP)
Erica Telford
(ANRS MIE)
Franck Touret
(Aix-Marseille University)
Astrid Vabret
(Caen University Hospital)
Hervé Watier
(Tours University)
This document presents the opinion of the AvATher group issued on February 18, 2025, regarding baloxavir marboxil (Xofluza®), a cap-dependent endonuclease inhibitor, in the context of the increasing outbreaks of highly pathogenic avian influenza (HPAI) H5N1 and the emergence of human cases of influenza A (H5N1).
The opinion outlines the antivirals currently authorized in the European Union and analyzes the available data on the virological and pharmacological efficacy of Xofluza®, particularly in comparison with other existing treatments. It also examines aspects related to virus transmission, administration protocols, and resistance management. Additionally, the document discusses relevant clinical studies and potential public health implications, particularly in comparison with oseltamivir.