Arbutus Biopharma (ABUS) Jefferies 2024 Global Healthcare Conference summary
Event summary combining transcript, slides, and related documents.
Jefferies 2024 Global Healthcare Conference summary
31 Jan, 2026Strategic vision and clinical focus
Aims to achieve a functional cure for hepatitis B using combination therapies of direct-acting antivirals and immunologics, targeting a cure rate of at least 20% with finite treatment duration.
Lead asset imdusiran (AB-729), a GalNAc-conjugated siRNA, is in multiple phase IIa trials (IMPROVE I, II, III) with various combinations, including interferon, VTP-300 vaccine, and durvalumab.
AB-101, an oral PD-L1 inhibitor, is in phase I development, with plans to combine it with imdusiran in future studies.
Strategic partnership with Qilu Pharmaceutical in China includes $40M upfront and $50M equity investment, expanding reach in the Asia Pacific region.
Strong cash position and ongoing patent litigation regarding LNP technology with Moderna and Pfizer, with a trial set for April 2025.
Clinical trial updates and data highlights
IMPROVE I phase IIa data showed 33% of patients achieved undetectable HBsAg and HBV DNA at end of treatment, with sustained S antigen loss and high HBV S antibodies.
Combination of imdusiran and VTP-300 vaccine demonstrated sustained S antigen reduction, with additional benefit from nivolumab in a third cohort.
IMPROVE-3 is evaluating imdusiran with durvalumab, targeting immune exhaustion via the PD-1/PD-L1 axis.
AB-101 demonstrated safety, receptor occupancy, and T cell function reconstitution in preclinical and early clinical studies.
Key opinion leaders consider functional cure rates above 15% clinically meaningful; further data expected by year-end.
Market and scientific rationale
Over 250 million people globally are affected by HBV, with significant prevalence in Asia Pacific due to limited vaccine access and mother-to-child transmission.
Combination therapy strategy aims to reduce HBV DNA, lower S antigen, and boost immune response for a finite, more tolerable treatment.
Imdusiran offers dosing every 8 weeks, robust S antigen declines, and immune reactivation, providing a competitive advantage.
Small molecule PD-L1 inhibitor AB-101 is designed to avoid immune-related adverse events seen with antibody therapies.
Latest events from Arbutus Biopharma
- $178.4M Moderna settlement drove profit, cash boost, and $230M return to shareholders planned.ABUS
Q2 2026 - Phase 2a trials show strong surface antigen loss and high nucleoside discontinuation rates.ABUS
H.C. Wainwright 5th Annual Viral Hepatitis Virtual Conference - Q1 2026 net income hit $169.7M on $178.7M settlement, with costs down and imdusiran advancing.ABUS
Q1 2026 - Key votes include director elections, incentive plan approval, say-on-pay, and auditor ratification.ABUS
Proxy filing - Key votes include director elections, equity plan approval, and auditor appointment at the 2026 meeting.ABUS
Proxy filing - $2.25B Moderna settlement and improved net loss highlight strong 2025 performance.ABUS
Q4 2025 - Imdusiran advances, cost cuts, and strong cash extend runway into Q4 2026.ABUS
Q2 2024 - Q3 2024 net loss narrowed, pipeline advanced, and cash runway extended into Q4 2026.ABUS
Q3 2024 - Imdusiran and novel immunotherapies show strong promise for hepatitis B functional cure.ABUS
H.C. Wainwright 26th Annual Global Investment Conference 2024