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Univariate associations between pre-LT variables and outcomes in post-LT year 1 were determined using Mann-Whitney U and Fishers exact tests

Methods: This analysis includes data from participants who have received at least 24 weeks ( 6 doses) of tobevibart 300 mg and elebsiran 200 mg subcutaneously every 4 weeks (Q4W) and are on nucleoside reverse transcriptase inhibitors in the ongoing MARCH, STRIVE, and THRIVE studies in participants with CHB (NCT04856085 and NCT05612581) and the SOLSTICE study in participants with CHD (NCT05461170)

doi: 10.1016/j.molcel.2021.08.018

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