Arbutus Biopharma Corporation announced new preliminary end-of-treatment data from the Phase 2a clinical trial in patients receiving ongoing standard-of-care nucleoside analogue therapy indicating that treatment with imdusiran, Arbutus’ RNAi therapeutic, followed by Barinthus Biotherapeutic’s T-cell stimulating immunotherapeutic, VTP-300, was generally safe, well-tolerated and led to maintenance of lower HBsAg levels during the post-treatment follow-up period in patients with cHBV.
June 6, 2024
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