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F1ash

02/12/18 11:30 AM

#140714 RE: Investor2014 #140712

None of us knows what feedback the FDA had on the Rett IND, but anyone is free to promote that it was something approaching a doomsday scenario



Let’s be clear, I never said it was a “doomsday scenario”.

I did suggest that the Rett girl’s communication difficulties in communicating side effects could complicate the IND application before it actually happened though.

Based on preclinical data, what dose would you predict they would like to use in the Rett trial? (I’ve asked several times now)
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tradersbend

02/12/18 1:42 PM

#140727 RE: Investor2014 #140712

You mean no brain bleeding or heart palpitations like the approved drug?
Sound like a short / stopped trial approval to me!