Arbutus Biopharma Corporation · NASDAQ:ABUS

Arbutus Biopharma — AASLD 2022

15 slides from Arbutus Biopharma's conference presentation, Nov 4, 2022

  1. Slide 1: AASLD Data Presentation

    NASDAQ: ABUS www.arbutusbio.com November 4, 2022 AASLD Data Presentation

  2. Slide 2: Forward-Looking Statements

    Forward - Looking Statements This presentation contains forward - looking statements within the meaning of the U . S . Private Securities Litigation Reform Act of 1995 and Canadian securities laws . All statements that are not historical facts are hereby identified as forward - looking statements fo

  3. Slide 3: AB-729-001 Phase 1a/1b Clinical Trial

    AB - 729 - 001 Phase 1a/1b Clinical Trial HBeAg : HBV E antigen | TDF: tenofovir disoproxil fumarate Part 3: Multiple Ascending Dose in cHBV Patients (n=7/cohort) E: 60mg Q4W HBV DNA - F: 60mg Q8W HBV DNA - G: 90mg Q8W + TDF HBV DNA+ I: 90mg Q8W HBV DNA - J: 90mg Q12W HBV DNA - K: 90mg Q8W HBV DNA -

  4. Slide 4: Robust HBsAg Declines Irrespective of Dose, Dosing Schedule, HBeAg or HBV DNA Status

    Robust HBsAg Declines Irrespective of Dose, Dosing Schedule, HBeAg or HBV DNA Status Mean (SE) Baseline and Δ log 10 HBsAg by Visit Data shown as mean (SE) log 10 IU/mL; HBsAg LLOQ = 0.07 IU/mL, <LLOQ defined as 0.035 IU/mL Last AB - 729 dose in Cohort K was at Week 40 *N=6; # N=5, 2 subjects did no

  5. Slide 5: Robust HBsAg Declines Persist After Stopping AB-729

    Data presented at AASLD 2022 5 Change in HBsAg vs time Robust HBsAg Declines Persist After Stopping AB - 729 33 of 41 patients had HBsAg < 100 IU/mL at some point during the trial 1 patient in Cohort E (baseline HBsAg = 583.5 IU/mL) who qualified but declined to participate in NA discontinuation ser

  6. Slide 6: HBV Control Maintained While Off-Treatment

    HBV Control Maintained While Off - Treatment Pt. 46 Pt. 51 Pt. 52 Pt. 53 Pt. 56 Pt. 58 Pt. 59 Pt. 60 Pt. 61 No patients have met virologic or clinical relapse criteria or restarted NA therapy to date HBV DNA has transiently increased in some patients and subsequently decreased with no intervention D

  7. Slide 7: AB-729-001 Safety Summary

    AE: Adverse Event | TEAE: Treatment Emergent Adverse Event 7 AB - 729 - 001 Safety Summary *1 patient (Cohort A) with rapid decline in HBsAg of ~2.0 log10 IU/mL had an unrelated Gr 2 AE of food poisoning resulting in unrelated transient Grade 3 AEs of ALT/AST elevation (without bilirubin changes) AB

  8. Slide 8: AB-729 Key Attributes

    Single trigger agent targeting all HBV transcripts Unique, proprietary GalNAc delivery technology AB - 729 Key Attributes 1.8 to 2.1 log 10 HBsAg decline in cHBV patients irrespective of dose, dosing interval or baseline characteristics Robust reduction in HBsAg with 48 weeks of treatment No evidenc

  9. Slide 9: Clinical Collaboration with Assembly

    Clinical Collaboration Provides accelerated AB - 729 combination POC with Assembly’s capsid inhibitor and a NA AB - 729 Follow Up (24 - weeks) AB - 729 (60mg) + VBR (300mg) + NA (n=32) AB - 729 + NA (n=17) VBR + NA (n=16) Baseline Wk 48 Wk 24 Primary objective: evaluate safety and tolerability of ve

  10. Slide 10: Preliminary Phase 2a Triple Combination Data

    10 Preliminary Phase 2a Triple Combination Data The proportion of patients who achieved HBsAg levels <100 IU/mL and <10 IU/mL was similar in patients who received VBR+AB - 729+NrtI and AB - 729+NrtI No patients experienced HBsAg loss or seroconversion At the time of this analysis 0/1, 2/2 (100%), an

  11. Slide 11: 3-Pronged Approach to Therapeutic Success

    Suppress Reduce Boost Viral DNA and cccDNA Pool Viral Antigen - HBsAg Host Immune System Leading to an HBV Cure 3 - Pronged Approach to Therapeutic Success Therapeutic success will require a combination of agents with complementary MOAs. Suppress HBV DNA Reduce viral antigens Boost host immune respo

  12. Slide 12: AB-101: Demonstrates Target Engagement in CD8+ Kupffer Cells in a cHBV Mouse Model

    12 AB - 101: Demonstrates Target Engagement in CD8+ Kupffer Cells in a c HBV Mouse Model GalNAc - siRNA s.c. AB - 101 10 mg/kg p.o. q.d . GalNAc - siRNA s.c. AB - 101 30 mg/kg p.o. q.d . Day 0 GalNAc - siRNA s.c. Vehicle p.o. q.d . Day 0 Day 21 Day 41 AB - 101 30 mg/kg p.o. q.d . Atezolizumab 10 mg/

  13. Slide 13: AB-101 + siRNA Combination: Increases HBV-Specific T Cell Activity and HBsAb

    13 AB - 101 + siRNA Combination: Increases HBV - Specific T Cell Activity and HBsAb in Liver Liver HBV - Specific T Cells Day 42 Ex vivo Fluorospot Data presented at AASLD 2022

  14. Slide 14: AB-101: Summary

    14 AB - 101: Summary Oral small - molecule PD - L1 inhibitors have been identified which function through a novel internalization mechanism distinct from antibody approaches Combination treatment with AB - 101 and HBV - targeting siRNA resulted in the activation of HBV - specific T cell and humoral

  15. Slide 15: Thank You

    Thank You

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