... with that, a poster is able to visit nidan's history and read his past posts. He was encouraging, helpful and reflected calm. mr, I think you are mistaken.
He has not posted since 8/26, so tomorrow is a month that he hasn't posted for the general public to read.
If anyone received a PM from him since, please let us know.
Otherwise, he be with bennyboy and ipulator. God bless all of them.
Peace, powerwalker
ANAVEX NOW ... RIGHT NOW ... MONO-STYLE ... for LIFE ... and for ALL AGES!!!
The “figure it outon the back of a napkin” comment sure didnt seem like we would be charging $3,000 a year for Rett patients. Maybe he mentioned some number that I cant recall but I think he is very optimistic that this will be a good starting revenue generator. Would be nice once revenue really starts pouring in to reduce what we charge for Rare diseases. Just doesnt seem right to charge a high price given the cards they have been dealt and the family members struggles (which are blessings in disguise)!
'Are they anticipating manufacturing and selling the drug on their own which is a big undertaking and very complicated'
If RETT approved, RETT foundation will let every patient/parent know... Although AVXL has manufacturing capability for RETT, it will require a partner for PDD, PD(motor), AD and other CNS drugs in the pipeline.
Another theory - ANVX might need another shelf(one already exists) for hostile takeover attempt after very good trial data is published. ALL IMHO.
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