EMA confirms risks of MS drug Zinbryta
The European Medicines Agency has concluded that the risks linked with use of Biogen and AbbVie’s multiple sclerosis drug Zinbryta outweigh its benefits.
Read Moreby Selina McKee | May 21, 2018 | News | 0
The European Medicines Agency has concluded that the risks linked with use of Biogen and AbbVie’s multiple sclerosis drug Zinbryta outweigh its benefits.
Read Moreby Selina McKee | Mar 8, 2018 | News | 0
The European Medicines Agency is now recommending the immediate suspension and recall of Biogen’s multiple sclerosis therapy Zinbryta, just days after announcing a safety review.
Read Moreby Selina McKee | Mar 5, 2018 | News | 0
European regulators have started an “urgent review” of Biogen and Abbvie’s multiple sclerosis therapy Zinbryta following a stream of cases of serious inflammatory brain disorders in patients taking the drug.
Read Moreby Selina McKee | Apr 11, 2017 | News | 0
Scotland will become the first UK nation to routinely offer HIV pre-exposure prophylaxis to all eligible patients after the Scottish Medicines Consortium backed the use of Gilead’s Truvada alongside four other new therapies to be funded by the NHS.
Read Moreby Selina McKee | Mar 16, 2017 | News | 0
Eligible patients with multiple sclerosis should be able to get routine access to Biogen’s Zinbryta on the NHS in the next few months following a green light from cost regulators.
Read Moreby Selina McKee | May 31, 2016 | News | 0
US patients with multiple sclerosis could soon gain access to a new treatment option after the US Food and Drug Administration approved Biogen and AbbVie’s once-monthly, self-administered subcutaneous injection Zinbryta.
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