>Another problem is that Kamada may not have enough of the active pharmaceutical ingredient (API) for inhalable API to treat all cystic fibrosis patients.<
Not enough API to make API? That sounds like circular reasoning
On a more serious note…
>…API will be approved for cystic fibrosis even before it is approved for the treatment of congenital emphysema. Approval for treating both diseases is expected before 2009.<
It takes chutzpah to display such confidence in an indication (CF) where prior attempts to use AAT failed (#msg-21040079). Could this be a case where the Hebrew to English translation came out wrong?
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”