Replies to post #19774 on Revive Therapeutics Ltd (RVVTF)

[rf101459]

The way I always viewed it is possible EUA at 210 data so one can get a script from Doc. But not likely finale approval till after data from 1000.

[RioDad]

Warrior,

I believe
At 210, the FDA will give green light for Emergency Use Authorization (EUA).
1000 patient trial should be completed and maybe even expanded so that other aspects can proven scientifically.

Now, why did I say ‘expanded’?

It’s my belief that the trial needs to start including measurements for antibodies, and strength of virus found in blood after 14, 28, 42, 60, and may be even 180 & 365 days.

I am going to make a Scientific hypothesis that Bucillamine may help those in the trial create a natural immunity.
If it can be taken for 14 days and cripple the virus and lessen “shed” then it is the Wonder Drug we’ve all hoped it can be.

Remember Coronavirus are not new, and Bucillamine could be used for a myriad of other illnesses & conditions.