Yes the call, created more questions than answers,
Post# of 148119
I posted this one yesterday but it deserves repeating:
“MHRA has recommended that Leronlimab might be a good candidate for Early access to Medicines Scheme or called EAMS. Under this EAMS approval patients in the UK will be allowed to have access to #leronlimab prior to it’s full marketing authorization."
I'm going to listen to that section again, but didn't Kush say they are already putting together for delivery everything MHRA has asked for to make a determination here? Given our safety profile the UK may just bang this out, to all our surprise.