SMC green light for rare blood cancer treatment
NHS funding was backed for four medicines
Read Moreby Selina McKee | Dec 10, 2019 | News | 0
NHS funding was backed for four medicines
Read Moreby Selina McKee | Dec 2, 2018 | News | 0
Shire has announced that the European Commission has approved its hereditary angioedema (HAE) drug Takhzyro.
Read Moreby Selina McKee | Nov 16, 2018 | News | 0
Shire says it presented data showing that its experimental drug lanadelumab provides a significant and clinically meaningful reduction of hereditary angioedema (HAE) attacks.
Read Moreby Selina McKee | Aug 24, 2018 | News | 0
Shire’s Takhzyro has been approved in the US for the prevention of attacks of hereditary angioedema (HAE) in patients 12 years of age and older.
Read Moreby Selina McKee | Mar 29, 2018 | News | 0
EU regulators have validated Shire’s application to market its experimental hereditary angioedema (HAE) drug lanadelumab, indicating that there is sufficient data to begin a priority review.
Read Moreby Selina McKee | Feb 28, 2018 | News | 0
European regulators will undertake an accelerated assessment of Shire’s hereditary angioedema (HAE) drug lanadelumab.
Read Moreby Selina McKee | Feb 23, 2018 | News | 0
US regulators are undertaking a speedy review of Shire’s lanadelumab (SHP643) for the prevention of angioedema attacks in patients 12 years and older with hereditary angioedema (HAE).
Read More





PharmaTimes Media Ltd.
44 Maiden Lane
Covent Garden
London
WC2E 7LN
E: editorial@pharmatimes.com
E: subscriptions@pharmatimes.com
T: +44 (0)20 7240 6999
