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Kb1123

06/22/21 8:40 PM

#316761 RE: infitvest #316760

It’s the overwhelming percentage of patients that select to go into the ole that is telling
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polarbear77

06/22/21 8:56 PM

#316763 RE: infitvest #316760

Excellent point, infitvest, and furthermore, if you were the parent of a Rett Syndrome-afflicted child, tell me you wouldn’t be effectively knocking down the door of your child’s neurologist’s office and/or the RS advocacy organizations to (essentially) demand immediate access to blarcamesine after reading yesterday’s results and slides and charts from our placebo controlled trial.

Wild horses could not keep me away.

No treatment currently available. Serious and debilitating rare disease of unmet need.

It’s time to provide these patients with our safe and very effective compound, and at an early enough age to slow/reverse the course of the disease.

Godspeed Anavex.

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98beamer

06/23/21 6:09 AM

#316788 RE: infitvest #316760

I ask myself this over and over...

If my child was taking an experimental drug (2-73) would I be "excited" if I didn't see progress or positive changes?



If my child was on this drug I would also have to consider they may be taking the placibo and this may be why I'm not seeing progress.