Monday, March 13, 2017 3:03:11 PM
First impressions: it is a long trial (240 weeks dosing), measures fibrosis stage reduction, for well compensated patients (MELD score below 12).
It seems to target a segment not covered by CNAT, ie compensated patients who do not necessarily have a High Portal Vein Pressure issue (hence they are not classified as at high risk of developing decompensation). I think was done on purpose to target a segment not currently covered by any other drugs under development, anyway top line results not earlier than 2020.
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