Just thinking out loud…
My understanding is that we (inclusive of all co- owners of MSB & not to be confused with the royal ‘WE’) are seeking approval to have Remestemcel-L made available on market for paediatric sr aGVHD. Should such approval be given by the fda, we would not be competing with Jakafi as it has already failed in those patients we would be treating.
Once the adult trial is concluded & should approval be given, would we then be competing for the entire market (adult & paediatric) & from what stage of the disease would our treatment be used?
I’m asking also because I am keen to determine the treatment side effects & whether side effects are the same for the entire market or just adults?
Also, do physicians take into account side effects when choosing treatments & are patients informed?
https://hcp.jakafi.com/acute-graft-versus-host-disease/
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