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Posted On: 01/30/2021 10:03:13 PM
Post# of 148899
As Nader mentioned Thursday evening in the Phillippines zoom call, the US FDA and the UK MHRA want the CD12 data as soon as it is unblinded.
I suspect the primary reason for this is because the primary endpoint is so simple and obvious.
If CD12 morality reduction is 30% or better the primary endpoint is hit, and everyone can move quickly to offer EUA.
The US FDA and UK MHRA know that they want to see the mortality reduction as soon as possible so they can be prepared to proceed?
I suspect the primary reason for this is because the primary endpoint is so simple and obvious.
If CD12 morality reduction is 30% or better the primary endpoint is hit, and everyone can move quickly to offer EUA.
The US FDA and UK MHRA know that they want to see the mortality reduction as soon as possible so they can be prepared to proceed?
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