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1. Do we know that Dr.BP started measuring viral load with the first patient in both trials? I know that the pre-print of his manuscript contained Plasma Viral Load graphs. Just not sure every trial subject was tested and documented that way.

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The viral load reduction would have been known before the trial started and the blood samples sent to IncellDX could have both serum and plasma separated for tests. So I have no doubt that was done.

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2. Is the FDA possibly so stringent in their submission regulations that there is facility for providing additional data points beyond what is officially included in the trial protocol?

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Any additional data that can support conclusions in the trial can be added in a supplement.

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