Mid 2008: Complete phase-1/2 IDX899 7-day monotherapy study using lower doses than 800mg. (Data from the 800mg cohort were reported on 2/6/08: #msg-26606685.) Report results at an unspecified conference.
3Q08: Start phase-2 IDX899 6-week combination study, IDX899+Truvada vs Sustiva+Truvada in first- or second-line patients.
2009: Partner IDX899 program following above phase-2 study.
HCV
April 2008: Report preclinical data on IDX184 ar EASL (#msg-27106080).