Thursday, 28 November 2013
European Medicines Agency recommends refusal of the marketing authorisation for masitinib
The European Medicines Agency Committee for Medicinal Products for Human Use (CHMP) has adopted a negative opinion, recommending the refusal of the marketing authorisation for the medicinal product masitinib (Masican), intended for the treatment of malignant gastrointestinal stromal tumour (GIST). Read more here.
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment