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Re: Midnight-Rider post# 164884

Wednesday, 05/12/2021 1:49:56 PM

Wednesday, May 12, 2021 1:49:56 PM

Post# of 232977
I agree, I finally realized that they have taken the CMC module information and since that is manufacturing data which really they don't control , they submit and claim they have started the process.

The fail point for CYDY is the clinical portion. It's possible all the EUA applications require results and passing P-Value which they do not have.

It's possible they are using these to kick the can down the road until they can get a successful trial, however that is way down the road, if ever.

This is why I saw the CSP and revenue from that as important, yet they went completely silent on that and skipped to EUA which I do not believe they will even complete the application for, much less receive the EUA.

If they can't get paid, then they definitely will not donate an expensive amount of LL to the Philippines , which may be what the Philippines FDA is pushing for.


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