Assembly Biosciences (ASMB) announced new preclinical and in vitro data for two therapeutic candidates featured in poster presentations, including one late-breaker, at the European Association for the Study of the Liver, EASL, Congress, taking place May 7-10, 2025, in Amsterdam, the Netherlands. The late-breaker poster presentation titled “Preclinical profiling of ABI-6250, a first-in-class oral therapeutic candidate for chronic hepatitis D” highlights preclinical data supporting the advancement of ABI-6250 into an ongoing Phase 1a clinical study. Results demonstrate that in cell culture, ABI-6250 specifically inhibits both HDV and hepatitis B virus at low nanomolar levels and shows selectivity versus a panel of other viruses. ABI-6250 showed minimal effects on cell viability in vitro across multiple cell types, and also selectively inhibited the sodium taurocholate cotransporting polypeptide bile acid transporter compared to a broad range of other transporters in vitro. The poster presentation titled “Sustained inhibition of HBV replication and HBsAg levels after long-term treatment with CAM ABI-4334 in human hepatocytes” describes in vitro studies of ABI-4334 evaluating multiple viral biomarkers of HBV infection. These results showed durable reduction in HBV nucleic acids and antigens in human hepatocytes following a one-month course of treatment with ABI-4334.
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