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Saturday, 12/31/2022 8:16:42 AM

Saturday, December 31, 2022 8:16:42 AM

Post# of 703411
After the ASM, I am pleased that everything with NWBO is moving forward, but I was left with 1 sad thought in my mind.

I know the RA's are there for the protection of the public. But I was struck with all the enormous amount of paper work, inspections etc., and TIME it takes to approve a new drug or vaccine. If 10 people had died and 100 had survived because of a clinical trial they would have been shut down immediately.

Let's take the UK only and GMB only. 12,000 GMB cases per year. A conservative 20% survival rate with DC Vac, That is 2400 patients that would be alive in 2 years of the approval process!! How did we get to this point? Remember scientist and doctors with PHD's have got this vaccine to the point of consideration by the RA's not snake oil sales men. Seems as if these all powerful, self-important agencies have gotten out of hand and are a determent to the advancement of medicine. Please do not crunch the numbers with all solid tumor cancers in 2 years all around the world.

Somebody restore my faith in the system for the new year.
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