Given the $195M in pre-commercial milestones expected from ABBV for regulatory filing ($40M in calendar 2Q14) and regulatory approval ($150M expected in early calendar 2015) of ABBV’s 3-DAA HCV regimen (#msg-91918990), it’s clear that ENTA does not have a liquidity probem.
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”