Neurotech International Ltd. · ASX:NTI

Neurotech International — Shareholder Meeting (November 2023)

17 slides from Neurotech International's shareholder meeting presentation, Nov 15, 2023

  1. Slide 1: Improving Lives – AGM Presentation

    For personal use only Improving Lives AGM Presentation Dr Tom Duthy Executive Director 15 November 2023

  2. Slide 2: Disclaimer

    Disclaimer IMPORTANT INFORMATION Purpose of presentation: This presentation (including this document, any related video or oral These events are, as at the date of this presentation, expected to take place, but there cannot be any guarantee that such will occur as anticipated, or at all, given that

  3. Slide 3: FY23 – A Year of Significant Progress

    FY23 – A Year of Significant Progress New Board & Executive Management Governance & Strategy For personal use only New Clinical and Development Focus New Bank/Broker Relationships Access to Capital Completed $9.0m Capital Raise Launched/reported new clinical trials Operational Execution Manufacturin

  4. Slide 4: Corporate / Capital Summary

    Corporate / Capital Summary $0.056 $49.4M $6.1M ~1,900 For personal use only Share price (as at 13 Nov 2023) Market Pro-Forma Cash No. of shareholders capitalisation as 30 Sept* 882.3M 116.3M^ $6.5M 53% Share on issue NTIOA (13.5c) + FY23 R&D Exp. Top 20 Holders (up from $2.6M in FY22) Other Options

  5. Slide 5: Neurotech is a clinical-stage biopharmaceutical development company

    Neurotech is a clinical-stage biopharmaceutical development company focused predominately on paediatric neurological disorders For personal use only NTI164 exclusive worldwide Novel oral Patents Pending – biopharmaceutical licence for neurological Use, Composition disorders cannabinoid platform (NTI

  6. Slide 6: Neurotech Four Core Strategies

    Neurotech Four Core Strategies For personal use only Focus On Rare Focus on Paediatric Patients Neurological Disorders with Neuroinflammation Focus on Partnering with Focus On Drug Product Key Opinion Leaders / Development Clinicians 6

  7. Slide 7: Clinical Pipeline – 2023

    Clinical Pipeline – 2023 Pre-Clinical Phase I/II Phase II/III For personal use only NTI164 NTI164 NTI164 Combination Therapies Prednisone, Diclofenac, Other Cerebral Palsy ASD Other Licensed NTI164 Strains PANDAS / PANS1 Pipeline (2020/1) NTI164 ASD NTI164 Combination Therapies (54 week open label e

  8. Slide 8: Therapeutic Agent: NTI164

    Therapeutic Agent: NTI164 THC < 0.3% For personal use only Convenient 1x or 2x (split dose) High potency, Broad Spectrum Cannabinoid Formulation in Oil, C. Major constituent Cannabidiolic oral formulation in oil, ideal acid (CBDA) format for pediatric patients sativa L. (Plant Derived) 20mg/kg (CBDA

  9. Slide 9: Developing NTI164 as a Therapeutic Agent

    Developing NTI164 as a Therapeutic Agent NTI164 will be registered as a prescription-only medicine For personal use only Neurotech investment into clinical trials to show safety and benefit Regulatory approval(s) will allow Neurotech to make a medical claim Significantly higher pricing and reimburse

  10. Slide 10: CBD OTC Market - Australia

    CBD OTC Market - Australia Highly Competitive, Low Margin, Low Price, Lack of Differentiation, Stringent Regulatory Oversight – Not the Market for NTI164 For personal use only 48 44/35 0 Number of over-the-counter (OTC) Domestic Manufacturers/ Importers CBD Products Registered on the CBD products ab

  11. Slide 11: CBD as a Drug – Significant Long-Term Upside

    CBD as a Drug – Significant Long-Term Upside TGA Approved Pharmaceutical Treatment – NTI164 Focus 1 1000mg A$24k For personal use only TGA Approved CBD oil CBD for 50kg child at 20 Epidiolex® cost per annum in (Epidiolex®) – 3 rare diseases mg/kg/day with Epidiolex® Australia (US$33k in USA) Strong

  12. Slide 12: Summary of Strategy

    Summary of Strategy Implementation Potential Group Strategy to Development Regulatory Levers Commercialisation Examples* Current 2016 2018/9 2021 For personal use only Phase I/II PANDAS/PANS Pre-IND Feedback IND Orphan Drug Designation Priority Review Phase III Trials US$7.2 Billion Phase I/II acqui

  13. Slide 13: Clinical Focus

    Clinical Focus ASD PANDAS/PANS Strong Scientific Rationale for NTI164 Cerebral Palsy • Anti-inflammatory effects + safety Rett Syndrome • Clinician support For personal use only • High Patient/Caregiver interest Neurological & Neuroinflammation Lack of effective treatments Rare / Orphan Paediatric O

  14. Slide 14: Our Target Markets

    Our Target Markets Lack of effective therapies, significant unmet medical need Annual Drug Therapy Market opportunity US$2 billion* US$2 billion US$1.4 billion1 US$4.3 billion For personal use only Orphan Orphan Autism Spectrum Disorder (ASD) Rett Syndrome PANDAS/PANS Cerebral Palsy (CP) • Prevalenc

  15. Slide 15: Key Milestones – NTI164

    Key Milestones – NTI164 1H CY2023 2H CY2023 • Final results of ASD Phase I/II Clinical Trial (52 weeks) • Commence Phase II Clinical Trial in Rett Syndrome For personal use only • Commencement of Patient Recruitment PANDAS/PANS Phase I/II • Results of PANDAS/PANS Phase I/II Clinical Trial Clinical T

  16. Slide 16: Outlook

    Outlook • Focus on rare paediatric neurological disorders • Accelerated clinical development via rapid & cost-effective proof of concept Phase I/II clinical trials in Australia for new paediatric neurological For personal use only disorders (PANDAS/PANS, Rett and CP) • Two further clinical trial rea

  17. Slide 17: Contact Details

    For personal use only Contact Details Dr Tom Duthy Executive Director td@neurotechinternational.com +61 402 493 727 *This presentation has been authorised by the Board of Neurotech International Limited www.neurotechinternational.com www.mentetech.com Neurotech International Limited (ASX: NTI) 17

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