Thanks for your input
Here’s the thing
If the readout re DMD trial is Stella good
FDA could give Per the green light as soon as end 24 ..
PER has stated that they will take the Tox first to the FDA
Then take the readout to the FDA soon after..
Because of the urgency for DMD sufferers there is no time to waste
FDA has set a precedence ..
We wait
Ann: Phase IIb study of ATL1102 in DMD completes recruitment, page-235
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