Aura Biosciences, Inc. · NASDAQ:AURA

Aura Biosciences — EAU 2025 Research Forum

12 slides from Aura Biosciences's conference presentation, March 2025

  1. Slide 1: Virus-like Drug Conjugates (VDC), a paradigm shifting approach for the treatment of bladder cancer

    Virus-like Drug Conjugates (VDC), a paradigm shifting approach for the treatment of bladder cancer Mechanism, First Insights, and Future Directions P . Black, Vancouver (CA), L. Bukavina, Philadelphia (US), S. Shariat, Vienna (AT) S. D. Brookman-May, Aura Biosciencs Boston (US), University of Munich

  2. Slide 2: Investigational Product Candidates

    Investigational Product Candidates This presentation discusses product candidates that are under preclinical or clinical evaluation and that have not yet been approved for marketing by the U.S. Food and Drug Administration (FDA) or any other regulatory authority. Until finalized in a clinical study

  3. Slide 3: Background – AU-011 (Bel-sar)

    Background – AU-011 (Bel-sar) Necrotic tumor cells Bel-sar • Current standard of care for NMIBC leaves a large, injection NIR light (689 nm) unmet medical need: DAMPS and neoantigens • High recurrence rates • Need for repeat surgeries and adjuvant treatments • AU-011 is a focally administered, Virus

  4. Slide 4: Phase 1 trial of bel-sar for bladder cancer designed to evaluate safety, feasibility, and mechanism of action

    Phase 1 trial of bel-sar for bladder cancer designed to evaluate safety, feasibility, and mechanism of action Single dose window of opportunity study in NMIBC all-comers Histopathological assessment completed at time of standard of care TURBT Part 1 (n=5) Part 2 (n=~10) bel-sar alone bel-sar + focal

  5. Slide 5: Efficacy data: Ta Intermediate-Risk NMIBC

    Efficacy data: Ta Intermediate-Risk NMIBC 4/5 patients demonstrated CR; 5/5 patients with immune response in target tumor aFor purposes of this analysis, Clinical complete response defined as absence of tumor cells on histopathologic evaluation. bBladder urothelial field effect: absence of tumor cel

  6. Slide 6: Efficacy data: Ta High-Risk NMIBC

    Efficacy data: Ta High-Risk NMIBC 1/5 patients demonstrated CR; 5/5 patients with immune response in target tumor aClinical complete response defined as absence of tumor cells on histopathologic evaluation. bBladder urothelial field effect: absence of tumor cells in non-target lesions. cImmune respo

  7. Slide 7: Visual and Immune Response in Patient A3: Intermediate-Risk NMIBC

    Visual and Immune Response in Patient A3: Intermediate-Risk NMIBC Tumor: Before bel-sar H&E: After bel-sar CD4: After bel-sar Tumor: After bel-sar Lymphoid follicles were observed, Significant infiltration of CD4+/CD8+ T-cells suggesting a strong adaptive immune in both treated and untreated tumors,

  8. Slide 8: Mature Tertiary Lymphoid Structures (TLS) in Target (Treated) Lesion

    Mature Tertiary Lymphoid Structures (TLS) in Target (Treated) Lesion: Active Immunosurveillance After Bel-sar Treatment CD3: T cells CD20: B cells CD23: Follicular Dendritic Cells (FDC) (Found in B cell follicles, only present in mature TLS) PNAd: Peripheral Node Addressin (Stains for high endotheli

  9. Slide 9: Early Tertiary Lymphoid Structures (TLS) in Distant Non-Target Lesion

    Early Tertiary Lymphoid Structures (TLS) in Distant Non- Target (Non-Treated) Lesion: Urothelial Immune Field Effect After Bel-sar Treatment CD3: T cells CD20: B cells CD23: Follicular Dendritic Cells (FDC) (Found in B cell follicles, only present in mature TLS) PNAd: Peripheral Node Addressin (Stai

  10. Slide 10: Summary and Conclusions Phase 1 Trial

    • Dual mechanism of action demonstrated with Virus-like Drug Conjugate: • Tumor cell necrosis with clinical complete response • Strong local immune response (active immunosurveillance) with generation of mature TLS • Extensive urothelial field effect in NMIBC with early TLS Summary and visualized in

  11. Slide 11: Future Directions for VDC Development in Bladder Cancer

    NIR light Necrotic tumor cells AU-011 injection DAMPS and neoantigens 1 Immune-ablative treatment without T cell trafficking and TURBT proliferation (LR/IR NMIBC) Activation of APCs Future Directions for VDC Development in Presentation of neoantigens to T cells Bladder Cancer IMMUNE ACTIVATION NIR l

  12. Slide 12: Panel Discussion

    Virus-like Drug Conjugates (VDC) Panel Discussion A paradigm shifting • Dr. Peter Black, Vancouver (CA) approach for the • Dr. Laura Bukavina, Cleveland (US) treatment of bladder cancer • Dr. Shahrokh Shariat (AUT) • Dr. Sabine Brookman-May (DE, US), Aura Biosciences, Mechanism Boston First Insights

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