Thursday, November 12, 2020 12:53:48 PM
B-C19 hopefully will change that, and I believe us to be on track to have a statistically significant clinical trial event lined up to precipitate something along the lines of a legitimate partnership (as opposed to a $400k one).
Having an overseas trial would bypass the wait for the IND approval (or default), and would expedite the timeline. Having biomarkers in place prior to an interim at 30 days (if it's a 2mo trial) will hopefully provide solid enough feedback to trigger a major partnership to move the indication significantly beyond what Leo would be able to do alone.
IMO, this is dead if Leo tries to go it alone.
(Reminder: The answering machine nonsense with the phone, the building lease, the uplist... etc, etc. )
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