Dimerix Limited · ASX:DXB

Dimerix — Investor Presentation (February 2022)

25 slides from Dimerix's investor presentation, Feb 24, 2022

  1. Slide 1: Investor Presentation February 2022

    @ Dimerix (ASX:DXB) Investor Presentation February 2022 Authorised for lodgment by the Board of the Company

  2. Slide 2: Forward looking statements

    Forward looking statements This presentation includes forward-looking statements that are subject to risks and uncertainties. Such statements involve known and unknown risks and important factors that may cause the actual results, performance or achievements of Dimerix to be materially different fro

  3. Slide 3: About Dimerix

    About Dimerix Dimerix is a biopharmaceutical company developing innovative new therapies in areas with unmet medical needs, with a core focus on developing new therapies to treat inflammatory causes of kidney and respiratory disease Advancing three ; rs % Phase 3 clinical studies i Wh w Demonstrated

  4. Slide 4: Share price and top shareholders

    For personal use only Share price Top shareholders

  5. Slide 5: Development pipeline

    Development pipeline Program Indication Preclinical Phase 1 Phase 2 Phase 3 Key milestones . Phase 2a demonstrated encouraging efficacy & safety’; Phase 3 underway (ac) Glomerular Sclerosis CF with regulatory &/or ethics authorisation in multiple countries’, recruitment of 1* patients planned Q1 22,

  6. Slide 6: Pro-inflammatory chemokines

    For personal use only Pro-inflammatory chemokines

  7. Slide 7: Kidney Disease Development Overview

    Kidney Disease Development Overview

  8. Slide 8: FSGS: unmet need and market potential

    FSGS: unmet need and market potential meXer]| =some 50% Segmental = sections of patients with Glomerulo = of the kidney filtering units FSGS will Sclerosis = are scarred Progress a kidney failure 20,000 FSGS patients in US have kidney failure “4000 FSGS patients in US receive a 2x more common “40,00

  9. Slide 9: FSGS phase 3 study design

    FSGS phase 3 study design nt ACTIAN3 A randomised, double-blind, multi-centre, placebo-controlled study of renal outcomes FSGS CLINICAL STUDY of DMX-200 in patients with primary FSGS receiving an ARB ARB stabilisation Treatment period weeks -6 -1 0 35 104 I il ! 6 oN 2 DMX-200 ® oI 2£f 2 2] = BI 3 a

  10. Slide 10: FSGS phase 3 study locations

    FSGS phase 3 study locations Global study with “70 sites in 12 countries: Count Regulatory and/or ethics y approval to proceed ACTIGNS Australia v Argentina v FSGS CLINICAL STUDY Brazil Denmark v France v A randomised, double-blind, multi-centre, placebo- Hong Kong controlled study of renal outcomes

  11. Slide 11: Patent protection and exclusivity

    For personal use only 1. If patent applications are granted: PCT/AU2022/050013; 2. DMX-200 is a New Chemical Entity (NCE): an active moiety not approved before which can attract exclusivity periods in various territories 3. Granted patents US9,314,450; US10,058,555; US10,525,038; CN2012800046165; CA

  12. Slide 12: COVID-19 Respiratory Complications

    COVID-19 Respiratory Complications

  13. Slide 13: COVID-19 and pneumonia market potential

    COVID-19 and pneumonia US$17 billion pre-COVID: Pneumonia responsible for US$17 billion in healthcare costs each year in the us! 3 million deaths annually caused by lower respiratory tract infections pre-COVID* hh 4.5 million: COVID-19: caused 219 million cases globally to date, resulting in >4.5 mi

  14. Slide 14: Potential benefits of DMX-200

    Potential benefits of DMX-200 Antiviral medications: Typically effective at preventing damage caused by a virus when administered days of infecti when many are asymptomatic 1. Brown L etal (2021) Early antiviral treatment in outpatients with COVID-19 (FLARE): a structured summary of a study protocol

  15. Slide 15: Two Phase 2 studies in COVID-19 patients

    Two Phase 3 studies in COVID-19 patients ss REMAP-CAP REMAP-CAP: COVID-19 pneumonia in ICU » >750 patients recruited to the study domain * WHO endorsed study * Primary endpoint = 21 day mortality Funded by European Union through H2020 “Rapid European COVID-19 Emergency Research response” (RECOVER) p

  16. Slide 16: Additional longer term propositions

    Additional longer term propositions

  17. Slide 17: Additional asset value propositions

    Additional asset value propositions Longer term opportunities Diversifying DMX-200 risk and Diabetic Kidney ferent Disease Uiee revenue Addressable market US$1.1 billion* Key driver is the rise in diabetes global incidence @ Dimerix 2017 IQVIA ARB prescription and pricing data; DMX-700 Chronic Obstr

  18. Slide 18: For personal use only

    For personal use only

  19. Slide 19: For personal use only

    For personal use only ✓ ✓ ✓ ✓ ✓ ✓ ✓ ✓ ✓ ✓ ❑ ❑ ❑ ❑ ❑ ❑

  20. Slide 20: Dimerix

    Dimerix A biopharmaceutical company developing innovative new therapies in areas with unmet medical needs, with a core focus on inflammatory disease treatments such as kidney and respiratory diseases. Advancing three Phase 3 opportunities Well positioned to deliver against strategic plan Dimerix HQ

  21. Slide 21: Appendix

    a@)\_ or personal use ‘= 7 _4 Dimerix, Appendix

  22. Slide 22: Phase 2a DMX-200-202 (ACTION for FSGS) study

    For personal use only Phase 2a DMX-200-202 (ACTION for FSGS): Phase 2a, Double-blind, Randomised, Placebo-Controlled, Crossover Study Evaluating the Safety and Efficacy of DMX-200 in Patients with Primary Focal Segmental Glomerulosclerosis who are Receiving Irbesartan • Primary endpoint: safety. Sec

  23. Slide 23: DMX-200 inflammatory biomarker

    DMX-200 inflammatory biomarker Average baseline MCP-1 versus average baseline proteinuria Dimerix Baseline uMCR (ng/mmol) 2 B =} S 1 Ny 8 L o o T T T 200 400 600 800 Baseline PCR (mg/mmol) 1 1000 DMX-200 Phase 2 study confirmed high MCP-1 correlates to high proteinuria in FSGS patients uMCR= Urinary

  24. Slide 24: Change in PCR ratio: DMX-200 vs placebo

    Geometric mean difference -17% For personal use only (95% CI -43 to +20; p0.25) 0 Change in PCR ratio (%) -10 -20 -30 -40 -50 PPG Placebo DMX-200 • • ▪ ▪

  25. Slide 25: DMX-200 treatment group met primary and secondary endpoints

    DMX-200 treatment group met primary and secondary endpoints Average reduction in proteinuria after 16 weeks treatment on DMX-200 versus placebo compared [app erloleel-vanrelaringclecveMel|-t-lmlet-tal-liimicod oy-le(-1a M1 gers) to standard of care alone in FSGS patients! 0.0% 2 2 5.0% £8 as <y £3 S

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