JJ I agree with your reply. Anavex is not going to market Blarcasamine as it doesnt have the expertise but what they do have is the wherewithal/expertise to get the drug approved and will imo.
These are difference times, I dont think our drug will be hard for a partner to market for Alz (PD/PDD off label) once it gets approved. This isnt a drug needing to be administered in a clinical setting and doesnt come with the black box warnings and AE’s. This coinciding with the new Alz early detection tests that are surfacing in the market place which will benefit our prophylactic conceptualization. If Dr M has manufacturing broken out I think we are looking at possibly even partnering with amazon for delivery which he has also stated now on the record.
As for rare diseases once we are approved the foundations will spread the news like wildfire and Dr.’s will not need to know about our drug, just give it too them initially and have a few follow ups, the rest will again come in the mail. I think Dr’s and middlemen marketers are stuck in pill pilfering, jabland and office setting visits. Thats all old fashioned once blarcasamine gets approved. I read somewhere AI has even become more efficient than nurses in following medication prescribing and avoiding complications from mistakes. Sad but inevitable.
Enough rambling from my tiny red so(lo)ap box.
Cheers