Arbutus Biopharma (NASDAQ:ABUS) has received regulatory clearance to initiate a Phase 1a/1b clinical trial of AB-729, a subcutaneously-administered RNA interference (RNAi) agent.
The Company was requested to complete its ongoing 3- and 6-month toxicology studies before commencing this trial. Based on further interaction with the regulatory authority, a revised protocol was submitted and Arbutus has received clearance to begin the Phase 1a/1b clinical trial.
AB-729-001 is a single and multiple dose clinical trial to investigate the safety, tolerability, pharmacokinetics, and pharmacodynamics of AB-729 administered by subcutaneous injection to healthy subjects and patients with chronic hepatitis B infection.
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