@Aaronfzr I vote c).
$1bn for DAYBUE ain’t happening any time soon. EU country level approvals will be slow, as once EU approval is given, $ACAD has to work with each member state has to work through price negotiations with national, public buyers.
Unlike US where private insurers are usually quick to add to their schedules once US FDA approves, in EU the country level process can take years. And even then, prices will be c. 70% of US, and accessibility will be lower and variable.
I sometimes wonder how well the covering analysts actually understand their markets.
Ho hum. At least we are agreed it’s worth a lot more than $14!
I am poised to add back more once we get the green light on start of PMS Phase 3. Surely can’t be long now. There aren’t many patients in the dataset to analyse and relatively few variables … trial size, end points. I’m sure Jon hasn’t given the whole team an extended summer break. So maybe FDA is taking its time answering emails, and between FDA, and the Board, the clinical team is in a bit of a do-loop?