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DewDiligence

04/03/23 5:53 PM

#2442 RE: Jake2234 #2441

If EDP-235 advances to phase-3, ENTA will likely seek to show non-inferiority to Paxlovid, which ought to be an achievable goal.

There is no FDA requirement that a COVID drug has to show any particular result for viral load or IVA to get approval.