Friday proved to be a good day for some of the world’s leading drugmakers, as the European Medicines Agency’s advisory unit, the Committee for Medicinal Products for Human Use (CHMP), came out with a batch of positive recommendations regarding European Union approval.
Backing for GSK/HGS’ Benlysta
Among these was UK-based GlaxoSmithKline (LSE: GSK) and US Partner Human Genome Sciences’ (Nasdaq: HGSI) lupus drug Benlysta (belimumab), which is intended as add-on therapy in adult patients with active autoantibody-positive systemic lupus erythematosus with a high degree of disease activity.
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