ARIA—If they were going for true 3rd-line (T315I or failed both 2nd line drugs) then I am pretty sure the FDA would approve.
For non-T315I patients, we’re really talking about a fourth-line treatment. ARIA longs dismiss Bosulif as irrelevant, but that’s no longer a tenable viewpoint, IMO.
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”