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abew4me

08/14/23 2:30 PM

#427317 RE: Investor2014 #427234

Yes it most certainly is.

Once A2-73 has obtained FDA approval for Rett, that is the disease the FDA has assigned to that drug.

Therefore, if Anavex plans to submit an NDA using A2-73 for Fragile X (or any other disease) without conducting a P1 or P2, then they are in fact repurposing that drug.