Shareholders here and @ RLF have been continuously screwed unless they have flipped to a profit after one pump or another. The feud and costly Delays seem to continue.*
I Expected!!! that the EAP data had been crunched already and presented WITH the CT data.
FDA may take as long as two months from application and NOW they will have to review the EAP data as 'supplemental supporting data' as well. More delays.
Questionable EUA may now need changing to full FDA approval review, IMO.
The Inhaler is using a slightly different formulation of RLF-100 IV.?. More shelf stable 'nebulized' formulation, but still needing sub-zero logistics.
They NEED to show Progress on the 'dry powder' formulations for future Inhaler use and CTs...ASAP.
Are ALL the data sets finally given to RLF for EMA? Will JJ stick his **** into that too?
*Historic betrayal issues.
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