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BioWorld - Sunday, February 8, 2026
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EMA validates MAA for Xyndari for sickle cell disease
March 13, 2018
Sigilon Therapeutics' SIG-003 awarded EMA ATMP designation
March 12, 2018
NTP-42 receives E.U., U.S. orphan designations for pulmonary arterial hypertension
March 8, 2018
Vocimagene amiretrorepvec/5-fluorocytosine granted E.U. orphan designation for glioma
March 8, 2018
EMA accepts regulatory submission for Forxiga in adults with type 1 diabetes
March 7, 2018
Gene therapy from Meiragtx receives European PRIME disgnation
March 5, 2018
EMA grants orphan drug designation to MTD-119 for hepatocellular carcinoma
March 1, 2018
EMA gives accelerated assessment to Shire's lanadelumab
Feb. 28, 2018
EMA grants orphan drug designation to cannabidiol for tuberous sclerosis
Feb. 28, 2018
EMA committee recommends change to marketing authorization terms for Feraccru
Feb. 26, 2018
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