** Shares of drugmaker Apellis Pharmaceuticals APLS.O fall
~1.2% to $65.49 premarket
** The European Medicines Agency (EMA) has recommended the
refusal of marketing authorization for Apellis' eye disease drug
Syfovre
** EMA says that the benefits of treatment should impact
patients' everyday functioning, and this was not demonstrated in
the studies for Syfovre
** Adds, the benefits of the drug did not outweigh its risks
** APLS plans to seek immediate re-examination of its
marketing application
** As of last close, stock up 25.5% in the last 12 months
(Reporting by Christy Santhosh)
((Christy.Santhosh@thomsonreuters.com))