InvestorsHub Logo
Followers 261
Posts 19732
Boards Moderated 0
Alias Born 10/03/2004

Re: bioinvestor10 post# 34933

Thursday, 07/01/2010 1:42:58 PM

Thursday, July 01, 2010 1:42:58 PM

Post# of 146240
Don't need FDA approval to generate income or increased value. Only need to progress to IND filing. There are funds and grants available long before FDA approval. Then, there is the orphan drug status/fast track/expedited review that kicks in once the tox work up is completed and when nanoviricides shows no adverse effects. Note I said when and not if.

There is a huge push to get this to Human testing and trials. There is also pressure due to immediate need to get this into compassionate use as quickly as possible. There is currently nothing out there, and the Sanofi solution is just another vaccine that if there are adverse effects they won't show up until late in trials and when clinical testing goes from hundreds of patients to 10s of thousands. That is the stage that all other vaccines have failed. I genuinely hope it does work, but I'm not putting any money over there, none at all.

Volume:
Day Range:
Bid:
Ask:
Last Trade Time:
Total Trades:
  • 1D
  • 1M
  • 3M
  • 6M
  • 1Y
  • 5Y
Recent NNVC News