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If you go back to the presentation made, either October 7 th or 8 th where the Dr. presented the data on Leronlimab he stated clearly that the FDA currently had the data for Cd12..or in his words ..and the FDA has the data as we speak....

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I did recall that and I don't profess to know the exact title or function of the individual Dr.HS was referring to.

Everyone is entitled to their own subjective view of this topic. However, I take Dr.NP's comment regarding no COVID EUA or Approval prior to Interim-293 at face value, and today's sleepy meeting does nothing to change my opinion.