Mesoblast believes that the totality of these clinical studies, together with additional potency assay data currently being generated using the IL-2R alpha inhibition potency assay in place during the pediatric Phase 3 trial, will both support approval for the pediatric indication and provide a link between the RYONCIL product that was used in the pediatric Phase 3 trial and available commercial inventory.
Still a week to go .Still think theres a kicker.
if not and the offer is not fully subscribed great less dilution.
I cant see its that big a deal.
The next decision from the FDA on the Assay Data is.
Remember the head of the department and the Blood and Bone
marrow transplant centre and Mesoblast were all present in person.
Just what did they agree on.?
Aloha.
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