Now that IH is up and running again, here is what

Now that IH is up and running again, here is what I have been thinking a lot about: the FDA received the raw CD-12 data as soon as it became unblinded weeks ago, and NP is now or imminently requesting EUA. Wouldn't the FDA have already told NP not to bother seeking EUA if it was a "no go" weeks ago from the FDA's perspective?