An external third party (pharma partner) will be the validation the market needs and could be seen as a measure of the strength of the AA chances from their perspective IMO .... who that partner / global pharma is and for what amount they contribute will be telling (again IMO) ....
..... chances are they have seen more Rexlemestrocel-L data through an NDA than the 'docs' on HC have (lol) so the size of their financial commitment will IMO be a measure / guidance as to their confidence in a successful FDA AA outcome for this indication ?
GLTAH
Ann: FDA Supports Accelerated Approval Pathway for Heart Failure, page-122
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