Sarepta's second shot at showing its Duchenne gene therapy delivers positive data but underwhelms — shares tumble
When Sarepta revealed last January that its gene therapy for Duchenne muscular dystrophy had failed the key functional endpoint in Part 1 of a Phase II trial, executives underscored that there’s a second part to the study — giving them another shot at a favorable readout.
One year later, Sarepta is taking the virtual podium at JP Morgan to present what they call positive results.
But reactions are decidedly mixed, and investors sent shares $SRPT tumbling 10.94% to $76.15.
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