I've seen a few posts, here and elsewhere, mention
Post# of 145747
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Obviously we'd all love to see that.
My question is, would that possibility (or not), or the odds of it, have been discussed in Cytodyn's recent FDA meeting? Curious if mgmt might touch on the subject in any future CC. Would love to know it's even remotely possible or whether we should all wind our necks in and assume P3 will be a must. Knowing what dicks the FDA have been, I'm going to keep said neck wound in.
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