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Re: Evil Rabbit post# 183620

Tuesday, 09/14/2021 12:35:33 PM

Tuesday, September 14, 2021 12:35:33 PM

Post# of 233200

Lol. Nice try. There is zero contamination. ANVISA wants reassurance that it won’t be an issue going forward, as they do with EVERY drug administered that way.

Here's what Nader himself said on the September 8th call:

But then Anvisa had a problem with the stability of the product in regards to particles that could be produced when you mix the Leronlimab in the IV bag and we had to do special tests. So we had to go to drawing board. Dr. Nitya Ray and his team did a fantastic job getting that test done very quickly and getting positive results, which we are very proud of, and getting that to Anvisa. The final report is either going to Anvisa today or it’s already been perhaps there.

You can't have it both ways. Either there was a problem (which Nader's own words seem to indicate), or this is a standard test that Cytodyn failed to perform in advance of starting the trial.

You can't seriously consider this guy as on the ball when we're burning $10-$13 million a month and he just wasted 3 months.
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