** Shares of drug developer Inovio INO.O rise ~8.7% to 39
cents premarket
** The U.S. FDA said early-stage data from Inovio's RRP
treatment trial can be used to submit a marketing application
for review under the FDA's accelerated approval program - INO
** Says co will be required to initiate a confirmatory trial
prior to submission and satisfy all other FDA filing
requirements
** Inovio says the FDA advised co's previously planned
late-stage trial would not be required to support this
submission
** RRP is characterized by the development of small,
wart-like growths, or papillomas, in the respiratory tract
** Up to last close, Inovio shares down 77% YTD
(Reporting by Christy Santhosh)
((Christy.Santhosh@thomsonreuters.com))