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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)

The stability of these DNA-AuNPs conjugates is significantly higher than that of analogues prepared from monothiols and cyclic disulfide-terminated oligodeoxyribonucleotides [74]

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