EU Marketing Authorisation change for Maviret
The authorisation shortens the treatment period from from 12 to eight weeks.
Read Moreby Anna Smith | Mar 9, 2020 | News | 0
The authorisation shortens the treatment period from from 12 to eight weeks.
Read Moreby Anna Smith | May 2, 2019 | News | 0
AbbVie’s Mavyret treats all six genotypes of hepatitis C virus.
Read Moreby Selina McKee | Nov 14, 2017 | News | 0
The Scottish Medicines Consortium (SMC) has published new advice accepting three new medicines for use by NHS Scotland, offering patients new treatment options for soft tissue sarcoma, acromegaly and hepatitis C
Read Moreby Selina McKee | Aug 4, 2017 | News | 0
AbbVie’s hepatitis C therapy Mavyret has picked up an approval in the US just days after having been green lighted by regulators in Europe.
Read Moreby Selina McKee | Jul 31, 2017 | News | 0
Patients with hepatitis C in Europe could soon gain access to two new pan-genotypic treatment options after the European Commission issued approval for AbbVie’s Maviret and Gilead’s Vosevi following an accelerated review.
Read Moreby Selina McKee | May 11, 2017 | News | 0
AbbVie’s glecaprevir/pibrentasvir (G/P) has become the first treatment for chronic hepatitis C to be included in the UK’s Early Access to Medicines Scheme (EAMS).
Read Moreby Selina McKee | Apr 21, 2017 | News | 0
AbbVie has released late-stage clinical data showing high cure rates for its experimental ribavirin-free hepatitis C therapy glecaprevir/pibrentasvir (G/P) across the majority of patients infected with the virus.
Read Moreby Selina McKee | Jan 24, 2017 | News | 0
European regulators are undertaking a speedy review of AbbVie’s investigational, pan-genotypic regimen of glecaprevir (ABT-493)/pibrentasvir (ABT-530) (G/P) for the treatment of chronic hepatitis C (HCV) in all major genotypes.
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