RE: Sponsor Access to Interim Data11 Feb 2022 10:23
Thanks for this Matml, really interesting to see that there is official FDA guidance for 'taking a peek' when there is an urgent need for the drug being studied.
This of course plays in to what just about every genuine holder here has been thinking for months. If we know it works, is safe, can save lives and potentially bring a genuine end to covid restrictions, why the hell don't governments know this!?!
I think the obvious answer is they do and they have been meticulously planning for the roll out of SNG for many months, clearing a path for approval, production and distribution of SNG001. RM has of course said as much in various interviews and panels over the last year.
I think it's good practice to take a step back and have a look at how truly unique this situation is relative to how drugs would be approved in the past. The fact that all of these dots are in the public domain for all of us to connect, because there is such a pressing need for the drug and it is of massive public interest.
Personally, I think production has already been established, approvals are a rubber stamp at this point and we are going to see INFb used in hospitals within the next 4-6 weeks. Governments will rightly want to take credit for supporting SNG and if the news drops and then the public is waiting months for the drug to be put in to action, against more deaths, long covid and restrictions, the backlash would be massive.
GLA and hold on tight to those golden tickets.