This page shows the latest baloxavir marboxil news and features for those working in and with pharma, biotech and healthcare.
Roche’s Xofluza (baloxavir marboxil) has been approved by the European Commission (EC) to treat and prevent uncomplicated influenza in children aged one year and over.
Roche has received approval from the US Food and Drug Administration (FDA) for a supplemental New Drug Application (sNDA) for Xofluza (baloxavir marboxil).
The EC has authorised Xofluza (baloxavir marboxil) for the treatment of uncomplicated influenza in patients aged 12 years and above.
Xofluza (baloxavir marboxil) is now indicated for use as a treatment to prevent influenza infection in people 12 years of age and above who have had contact with someone with influenza.
The CHMP has recommended Xofluza (baloxavir marboxil) for approval in the EU as a treatment for uncomplicated influenza patients aged 12 years and above.
Expands use to patients at high risk of flu-related complications. Roche’s Xofluza (baloxavir marboxil) has received FDA approval for use in people who have a high risk of developing
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