– ABI-4334 was well-tolerated with a favorable safety profile and half-life supporting once-daily oral dosing observed –
– In the first 150 mg dose cohort, ABI-4334 showed strong antiviral activity with a mean reduction of 2.9 log IU/mL in plasma HBV DNA over 28 days of treatment –
– Enrollment in final cohort of 400 mg ongoing with data anticipated in 1H 2025 –
No comments:
Post a Comment
Note: Only a member of this blog may post a comment.