Agree with you, lets hope MSB holds. Could not reply Col's post so borrowing tour instead
Col
I was talking about the final report to the FDA. The next line after your quote reads "The final module will be filed during January, and Mesoblast will request an expedited FDA review of the BLA under the product candidate’s existing Fast Track designation. If approved, remestemcel-L is planned to be launched in the US in 2020."That should be very clear what was filed and what was not.
MSB Trading - 2020, page-1524
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