Alterity Therapeutics Ltd. · ASX:ATH

Alterity Therapeutics — Shareholder Meeting (November 2023)

26 slides from Alterity Therapeutics's shareholder meeting presentation, Nov 29, 2023

  1. Slide 1: Alterity Therapeutics

    For personal use only Alterity Therapeutics (NASDAQ:ATHE, ASX:ATH) David Stamler, MD November 2023 CEO

  2. Slide 2: Forward Looking Statements

    For personal use only Forward Looking Statements This presentation may contain some statements that may be considered “Forward-Looking Statements”, within the meaning of the US Securities Laws. Thus, any forward-looking statement relating to financial projections or other statements relating to the

  3. Slide 3: Alterity is dedicated to being different

    For personal use only Alterity means the state of Alterity is dedicated to being different creating an alternate future for people living with neurodegenerative Our goal is to modify the course of disease diseases. We’re here to disrupt the trajectory of illness and improve quality of life 3

  4. Slide 4: Investment Highlights

    Investment Highlights For personal use only • Developing disease modifying therapies • ATH434: Novel drug candidate targeting proteins implicated in neurodegeneration of Parkinson’s disease and related disorders • First indication: Multiple System Atrophy (MSA), a parkinsonian disorder with no appro

  5. Slide 5: Experienced Leadership Team with Multiple FDA Approvals in Neurology

    Experienced Leadership Team with Multiple FDA Approvals in Neurology For personal use only David Stamler, M.D. Kathryn Andrews, CPA Margaret Bradbury, Ph.D. Cynthia Wong, M.P.H. Chief Executive Officer Chief Financial Officer VP, Nonclinical Development Senior Director, Clinical Operations Auspex/Te

  6. Slide 6: Parkinsonian Disorders: A Significant Unmet Need

    Parkinsonian Disorders: A Significant Unmet Need • Parkinsonism is a syndrome of motor symptoms that For personal use only PARKINSONIAN DISORDERS includes slowed movement, stiffness and tremor • Parkinson’s disease most common cause • Major source of disability MSA • Parkinsonian disorders include M

  7. Slide 7: Promising Portfolio in Neurodegenerative Diseases

    Promising Portfolio in Neurodegenerative Diseases For personal use only ASSET PHASE PARTNER PRE- NATURAL PARTNER / PROGRAM INDICATION DISCOVERY PHASE 1 PHASE 2 CLINICAL HISTORY COLLABORATOR Multiple System Atrophy ATH434-201 Early Stage Multiple System Atrophy ATH434-202 Advanced Multiple System Atr

  8. Slide 8: The Role of Alpha-Synuclein and Iron in Parkinsonian Disorders

    For personal use only The Role of Alpha-Synuclein and Iron in Parkinsonian Disorders 8

  9. Slide 9: Alpha-Synuclein: Critical for Normal Neuron Function

    Alpha-Synuclein: Critical for Normal Neuron Function For personal use only Our Strategy • Inhibit misfolding and aggregation of intracellular α‐synuclein • Target misfolding α-synuclein by redistributing loosely bound excess iron in areas of pathology • Address underlying pathology of disease α-Synu

  10. Slide 10: Increased Brain Iron in Synuclein-related Diseases

    Increased Brain Iron in Synuclein-related Diseases Parkinson’s disease Multiple System Atrophy For personal use only n=7 * Patients Substantia nigra (T) n=8 n=9 Cerebral cortex Healthy n = 11 n=8 * Substantia nigra (pc) n=3 n=8 * Caudate nucleus n = 13 n = 10 Cerebellum n = 24 n=8 * 0 10000 20000 30

  11. Slide 11: Iron: Critical in Disease Pathogenesis

    Iron: Critical in Disease Pathogenesis For personal use only α-Synuclein and iron are strong contributors to Oxidative Stress the pathology of MSA • Adverse impact of excess loosely bound iron • Promotes α-synuclein aggregation • Root cause of oxidative stress which damages intracellular structures

  12. Slide 12: Approach: Address Underlying Pathology of Disease

    Approach: Address Underlying Pathology of Disease For personal use only Reduce α‐synuclein Redistribute excess iron aggregation Rescue neuronal in the Central Nervous System and function Oxidative stress Potential Disease Modifying Therapy for MSA 12

  13. Slide 13: ATH434: Disease Modifying Drug Candidate

    ATH434: Disease Modifying Drug Candidate • Small molecule drug candidate that reduces α-synuclein For personal use only aggregation • Iron chaperone, redistributes loosely bound excess iron in brain • Oral agent (tablet) for ease of use • Readily absorbed, shown to reach site of action in man • Pote

  14. Slide 14: Multiple System Atrophy Clinical Development Program

    For personal use only Multiple System Atrophy Clinical Development Program 14

  15. Slide 15: Multiple System Atrophy is a Rare, Highly Debilitating Neurodegenerative Disorder

    Multiple System Atrophy (MSA) is a Rare, Highly Debilitating and Rapidly Progressive Neurodegenerative Disorder For personal use only • Clinical impairments include • Motor: Parkinsonism, uncoordinated movements, balance problems/falls • Autonomic dysfunction: Reduced ability to maintain blood press

  16. Slide 16: Completed Phase 1 with Favorable Safety Profile

    Completed Phase 1 with Favorable Safety Profile ATH434 Levels at Steady-State For personal use only 250 Plasma (unbound, ng/mL) • Achieved drug concentrations associated 200 with efficacy in animal models 150 100 50 r2=0.72 • Adverse Events (AEs) 0 0 50 100 150 200 250 CSF (ng/mL) • No SAEs or AEs l

  17. Slide 17: bioMUSE: Natural History Study in MSA

    bioMUSE: Natural History Study in MSA For personal use only Design • Observational • Design and de-risk Phase 2 Objectives • Identify biomarker endpoints for treatment study • Early-stage MSA patients similar to Phase 2 population Population • ~20 participants Observation • 12 months Period • MRI: I

  18. Slide 18: bioMUSE Natural History Study

    bioMUSE Natural History Study Design and De-risk Phase 2 New MRI Template Advanced MRI methods For personal use only Optimize Patient Selection Assess Endpoints with Precision Pilot Clinical Measures Identify “iron signature” Improve precision of iron in early MSA vs. PD quantification by MRI Wearab

  19. Slide 19: ATH434-201: Randomized Phase 2 Clinical Trial in Early-Stage MSA

    ATH434-201: Randomized Phase 2 Clinical Trial in Early-Stage MSA For personal use only Design • Randomized, double-blind, placebo controlled • Assess efficacy and safety of ATH434 in participants with MSA Objectives • Assess target engagement based on imaging and fluid biomarkers Population • Early-

  20. Slide 20: ATH434-201 Phase 2 Design and Primary Endpoint

    ATH434-201 Phase 2 Design and Primary Endpoint For personal use only Primary Endpoint: Change in Brain Iron on MRI 0.30 Iron Content (GPe) 0.25 0.20 0.15 R² = 0.63 0.10 0.05 0.00 0 20 40 60 80 Unified MSA Rating Scale BioMUSE Natural History Study Demonstrates Brain iron correlates with disease seve

  21. Slide 21: Patient Specific Map to Evaluate Primary Endpoint with Precision

    Patient Specific “Map” to Evaluate Primary Endpoint with Precision ATH434 targets increased iron in For personal use only patient-specific Region of Interest Iron Distribution Age Distribution of brain iron varies Patient Map Patient’s age among MSA determines the patients Generates patient specific

  22. Slide 22: ATH434-202: Phase 2 Biomarker Trial in MSA

    ATH434-202: Phase 2 Biomarker Trial in MSA For personal use only Design • Single arm, open-label • Assess target engagement based on imaging and fluid biomarkers Objectives • Assess efficacy and safety of ATH434 in participants with MSA Population • Clinically Established (advanced) MSA with biomark

  23. Slide 23: Significant Commercial Opportunity in Treating Multiple System Atrophy

    Significant Commercial Opportunity in Treating Multiple System Atrophy For personal use only Substantial Unmet Need Strong Intent to Prescribe Severely debilitating illnesses Motivated by efficacy of treating with no current treatments are the underlying disease and not ripe for new entrants targeti

  24. Slide 24: Alterity: Poised for Progress

    Alterity: Poised for Progress Clinical Milestones For personal use only • Targeting Orphan disease with no approved treatments ATH434-201 Phase 2 Double-Blind Trial  Q1 2023: First Patients Dosed in U.S. • Two Phase 2 clinical trials ongoing and Europe • Double-blind trial enrolling globally  Q2 2

  25. Slide 25: Key Milestones

    Key Milestones For personal use only Enrollment Complete ATH434-201 Phase 2 Trial Data with ATH434 in Monkey Model Study Complete of Parkinson’s ATH434-201 Disease Phase 2 Trial bioMUSE Data Preliminary Data from ATH434-202 Open Label Biomarker Trial Oct Nov Dec Jan Feb Mar Apr May Jun July Aug Sep

  26. Slide 26: For personal use only

    off. Alterity For personal use only

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