Argenica Therapeutics Ltd · ASX:AGN

Argenica Therapeutics — Techknow Investor Presentation (July 2026)

19 slides from Argenica Therapeutics's conference presentation, July 2026

  1. Slide 1: Precision Neuroprotection for Severe Brain Injury

    Precision Neuroprotection for Severe Brain Injury ARGENICA THERAPEUTICS Targeting patients where brain injury – and value – is greatest TECHKNOW INVESTOR PRESENTATION ASX:AGN JULY 2026 DR LIZ DALLIMORE - MANAGING DIRECTOR PRESENTATION 1 www.argenica.com.au

  2. Slide 2: Disclaimer

    DISCLAIMER This presentation has been prepared by Argenica Therapeutics Limited and its related entities (the “Company”) and is not an offer document. It does not purport to contain all the information that a prospective investor may require in connection with any potential investment in the Company

  3. Slide 3: Investment Overview

    INVESTMENT OVERVIEW PRECISION NEUROPROTECTION APPROACH TO SEVERE BRAIN INJURY SCIENTIFICALLY VALIDATED FIRST-IN-CLASS NEUROPROTECTIVE DRUG Xaranetide (ARG-007) is a neuroprotective therapy targeting acute and secondary brain injury, with extensive preclinical efficacy data published on the ability o

  4. Slide 4: Key Company Metrics

    KEY COMPANY METRICS $6.4M $20M FY26 CASH @ BANK 1 MARKET CAP2 R&D Tax Rebate Expected H2 ARGENICA THERAPEUTICS 128.5M 37% SHARES HELD BY TOP 20 +ve DATA SHARES ON ISSUE IN PHASE 2 STROKE TRIAL 1. Cash balance as @ 30 June 2026 4 2. Calculated with closing price on @ 23rd July 2026 being $0.155 www.a

  5. Slide 5: Ischaemic Stroke Opportunity

    ISCHAEMIC STROKE ARGENICA THERAPEUTICS OPPORTUNITY 5 www.argenica.com.au

  6. Slide 6: Stroke Has the Greatest Incidence of Disability and Death

    STROKE HAS THE GREATEST INCIDENCE OF DISABILITY AND DEATH OF ALL NEUROLOGICAL CONDITIONS1 • Stroke is the leading neurological cause of long-term disability and death, significantly greater than other leading neurological conditions. • Stroke-related costs in the United States came to nearly $56.5 b

  7. Slide 7: Xaranetide's Unique Mechanism of Action to Reduce Multiple Causes of Brain Injury

    XARANETIDE’S UNIQUE MECHANISM OF ACTION TO REDUCE MULTIPLE CAUSES OF BRAIN INJURY ARGENICA THERAPEUTICS 7 Values in graphic approximated from Edwards et al., Mol Brain 2018 11(1):8 and Chiu et al., 2020. Curr Ther Res Clin Exp. 19:92:100584 for illustrative purposes www.argenica.com.au

  8. Slide 8: Key Benefits of Xaranetide Peptide Drug

    KEY BENEFITS OF XARANETIDE PEPTIDE DRUG PRODUCT  Powdered peptide reconstituted in saline and stable for up to 2 years* CONVIENIENT  Easy to store at 4°C (fridge) in 10mL vials & STABLE  Simple to inject into IV bag when ready to use ARGENICA THERAPEUTICS  Immediately available at point of care

  9. Slide 9: Phase 2 Trial Results

    PHASE 2 TRIAL ARGENICA THERAPEUTICS RESULTS 9 www.argenica.com.au

  10. Slide 10: Phase 2 Trial Design

    PATIENT HAS A PATIENT IN ARRIVES AT DIAGNOSE REHAB STROKE AMBULANCE HOSPITAL STROKE TYPE THROMBECTOMY BEGINS ARGENICA THERAPEUTICS Initial screening of Administration of Endpoints patients to meet inclusion 0.3mg/kg ARG-007 or Mortality rate and frequency of Adverse and Serious criteria saline place

  11. Slide 11: Phase 2 Post Hoc Results

    The Phase 2 trial identified a treatment effect in more severe stroke patients, paving the way for a precision-designed Phase 2b trial PHASE 2 POST HOC RESULTS • Whilst no overall effect was seen across the broader patient group due to baseline stroke severity imbalance ARGENICA THERAPEUTICS and ina

  12. Slide 12: ARG-007 Significantly Reduces Growth of Damaged Brain

    ARG-007 significantly reduces growth of damaged brain in moderate to severe stroke patients ARGENICA THERAPEUTICS Figure 1: Total corrected ischaemic lesion volumes (cISC) in ml as predicted from the corresponding multivariate model across different baseline AIV values (0ml, 10ml, 20ml; 30 ml). The

  13. Slide 13: Moderate to Severe Stroke Patients Have Reduced Disability Following ARG-007 Treatment

    Moderate to severe stroke patients have reduced disability following ARG-007 treatment ARGENICA THERAPEUTICS Figure 2: In multivariate analysis there was a significant interaction between infarct core size and treatment effect on clinical outcomes, specifically the modified rankin scale. Patients wi

  14. Slide 14: ARG-007 Significantly Improved Disability Outcomes in Patients with More Severe Strokes

    ARG-007 significantly improved disability outcomes in patients with more severe strokes ABLE TO WALK WITHOUT ASSISTANCE ARGENICA THERAPEUTICS Figure 3: Distribution of the mRS at 90 days across treatment arms using e-ASPECTS or AIV to exclude patients with small infarct cores alongside patients with

  15. Slide 15: FDA Clinical Hold Update

    FDA CLINICAL HOLD UPDATE The three safety assays requested by the FDA are now complete, with ARG-007 showing a clean safety profile across all three assays. Comprehensive clinical hold response to be submitted to FDA within weeks. FDA-Requested Assay Status Outcome Tenecteplase (TNK) Drug-Drug Inter

  16. Slide 16: Late-Stage Trial: Designed to Prove Efficacy in Moderate to Severe Strokes

    LATE-STAGE TRIAL: DESIGNED TO PROVE EFFICACY IN MODERATE TO SEVERE STROKES  Moderate to severe stroke (ASPECTS 3-8, AI assisted interpretation) PATIENT  Large Vessel Occlusion undergoing thrombectomy POPULATION  With or without thrombolysis ARGENICA THERAPEUTICS  mRS shift 90 days ENDPOINT  mRS

  17. Slide 17: Traumatic Brain Injury Update

    TRAUMATIC BRAIN INJURY UPDATE PROGRESS TOWARDS PHASE 1B TRIAL IN MODERATE TO SEVERE TBI ESTABLISHING PARTNERSHIPS WITH LEADING AUSTRALIAN INSTITUTIONS Argenica is in the final stages of engaging a number of hospital and academic institutions to establish collaboration agreements to execute the Phase

  18. Slide 18: Potential Catalysts for 2026

    POTENTIAL CATALYSTS FOR 2026  Complete responses to IND Clinical Hold H2  US IND Approval for ARG-007 in Stroke 2026  HREC Approval for ARG-007 in Stroke  Completion of large-scale manufacturing of clinical trial batches for clinical trials in stroke and TBI  Stroke Phase 2b Trial Site identifi

  19. Slide 19: For Further Information Please Contact

    ARGENICA THERAPEUTICS For further information please contact: Dr Liz Dallimore CEO & Managing Director E: info@argenica.com.au 19 www.argenica.com.au

Argenica Therapeutics — Techknow Investor Presentation (July 2026) on 6ix