Wolly99
$ALT FWIW: I'm hearing that FDA is strongly considering VCTE as a RLSE but only in combination with a concurrent drop in ELF. So instead of # of people on drug who had a drop in VCTE ≥30% compared to placebo, it'd be VCTE drop of ≥30% AND a drop in ELF of -0.5 units. VCTE+ELF to simplify.
Of note, ALT just released this data via AASLD abstracts:
1.8mg = 32.4% VCTE+ELF responders at 48W compared to just 6% pbo (p<0.0001)
This matches survo almost exactly. EFX didn't hit ≥30% reduction at week 24, but hit ~50% VCTE+ELF with the high dose at week 96 vs 6% pbo.
So figure with efx high dose at just 48 weeks (not 96), it'd project to be about 40% dual VCTE+ELF responders. And pemvi 2.4mg (not 1.8mg) would be maybe right under that around 37-39% - beating survo.
53
