No it is not the correct interpretation.
Company guidance was as below- no time frame- they have now , as per last presentation, said second half of the year.
Mesoblast intends to request a pre-BLA meeting with FDA to discuss data presentation, timing and
FDA expectations for an accelerated approval filing in ischemic HFrEF patients with end-stage heart
failure.
Come back July 1
Reg
banter and General Discussion, page-9965
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