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Re: A deleted message

Tuesday, 04/07/2020 6:23:23 PM

Tuesday, April 07, 2020 6:23:23 PM

Post# of 233119
Company plans on submitting data on the first ten patients treated on emergency IND. They are going to ask for emergency approval from the FDA.

What do you think their chances are?

Say

All ten patients were in severe condition and were on a ventilator. They are now doing great and off the ventilator.

Can the FDA grant provisional approval based upon results on the two ongoing trials? Have you ever seen anything like this.

What does the FDA have to lose?

200,000 dead patients waiting for more results.

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