Sequana Medical N.v · EURONEXT:SEQUA

Sequana Medical — H.C. Wainwright Global Life Sciences Conference 2021

27 slides from Sequana Medical's conference presentation, Mar 4, 2021

  1. Slide 1: Innovators in the treatment of diuretic-resistant fluid overload

    Innovators in the treatment of diuretic-resistant fluid overload liver disease – malignant ascites – heart failure H.C. Wainwright Global Life Sciences Conference Ian Crosbie, CEO – 4 March 2021

  2. Slide 2: Disclaimers

    Disclaimers Important Notice IMPORTANT: You must read the following before continuing. The following applies to this document, the oral presentation of the information in this document by Sequana Medical NV (the "Company") or any person on behalf of the Company, and any question-and-answer session t

  3. Slide 3: Disclaimers

    Disclaimers Regulatory disclaimer: • The alfapump® system has not yet received regulatory approval in the United States and Canada. Any statement in this presentation about safety and efficacy of the alfapump® system does not apply to the United States and Canada. In the United States and Canada, th

  4. Slide 4: Sequana Medical NV

    Sequana Medical NV Founded in 2006 Gent, Belgium (HQ): corporate, clinical, commercial Zurich, Switzerland: manufacturing, engineering, QA/RA ~50 employees Euronext Brussels: SEQUA 4

  5. Slide 5: alfapump platform

    alfapump® platform Using the bladder to treat fluid overload Fully implanted Easy implantation Long-term implantation & catheter Automatic operation patency Wireless battery charging Moves up to 4 litres / day Settings wirelessly adjusted Virtually non-clogging Remote data monitoring No significant

  6. Slide 6: One platform – two products – € billion opportunities

    One platform – two products – € billion opportunities alfapump® alfapump DSR® Liver Disease (NASH) Heart Failure Proven step change in liver refractory ascites Breakthrough approach to fluid overload in and malignant ascites heart failure Over 850 devices implanted Clinical proof-of-concept of Direc

  7. Slide 7: NASH drives US market attractiveness

    NASH drives US market attractiveness Stronger competitive position in a much larger and dynamic market alfapump® market potential ~€0.4 Bn / year >€3 Bn / year Underlying disease Alcoholic Liver Disease, Hepatitis NASH Patient characteristic “Outside mainstream” “Mainstream” Average age 40-50 yr 70

  8. Slide 8: alfapump

    alfapump ® Proven step change in the management of liver refractory ascites and malignant ascites

  9. Slide 9: Liver cirrhosis and refractory ascites

    Liver cirrhosis and refractory ascites A key complication of liver cirrhosis, with a dramatic impact on quality of life US forecast ~3-4M (1) Viral infections Liver (Hepatitis B & C) “Normal Life” cirrhosis ~5 days ~1.5M Decreased (2) High mortality rate mobility & Alcoholic Liver appetite, Ascites

  10. Slide 10: alfapump for long-term treatment

    alfapump® for long-term treatment Over 850 implants and hundreds of years of patient experience Breakthrough Device Designation 10 10

  11. Slide 11: North American Pivotal Study (POSEIDON) underway

    North American Pivotal Study (POSEIDON) underway Pivotal Cohort of up to 50 patients implanted; Roll-In (“training”) cohort of up to 30 patients alfapump Primary Secondary Enrolment implantation endpoint endpoints 3 months 3 months 3 months 18 months Pre-implant Post-implant Post-implant Post-implan

  12. Slide 12: POSEIDON Interim Data: Positive for primary endpoints

    POSEIDON Interim Data: Positive for primary endpoints Data from first 13 Roll-In patients EFFICACY Mean values post-implant vs. pre-implant N = 13 Reduction in frequency of TP > 90% Patients with >50% reduction in TP 100% SAFETY • Safety profile of the alfapump consistent with previously reported da

  13. Slide 13: Quality of Life: Indication of fast and persistent improvement

    Quality of Life: Indication of fast and persistent improvement Physical Component Score 5 point improvement = clinically relevant Higher is better SF-36 General health- survey questionnaire Total Score 20 point reduction = clinically relevant Ascites Q Specific health- survey questionnaire for ascit

  14. Slide 14: Targeting announcement of primary endpoint in Q1 2022

    Targeting announcement of primary endpoint in Q1 2022 2019 2020 2021 2022 FDA IDE First Interim Last Full Primary approval  patient in analysis 1  patient interim Endpoint in* analysis* Reporting* FDA breakthrough Filing* designation  Building out US team Final CMS rule for automatic Medicare co

  15. Slide 15: US commercialisation through our specialty salesforce

    US commercialisation through our specialty salesforce NY MI (7) (4) PA (12) OH Initial focus on key IL (6) (6) CA transplant centres (12) NC (3) ~50-person team: AZ (5) 35 sales reps, 10 clinical, GA (3) 5 corporate TX (13) FL (8) POSEIDON site Target State (# transplant centres) 15 15

  16. Slide 16: alfapump DSR

    alfapump DSR ® Breakthrough approach to fluid overload in heart failure built on proven alfapump® platform

  17. Slide 17: Diuretic-resistant fluid overload in heart failure

    Diuretic-resistant fluid overload in heart failure Key clinical challenge and driver of costs US hospitalisations HF – annually due to ~1m 90% hospitalisations HF(3) due to fluid overload(3) Excess sodium drives c.5d Typical fluid overload Annual costs of US hospital stay(4) HF-related $13bn hospita

  18. Slide 18: Direct Sodium Removal (DSR)

    Direct Sodium Removal (DSR®) Proprietary approach to fluid overload – supported by interim RED DESERT clinical data We remove the sodium and then the body “does the math” to maintain serum sodium balance DSR therapy directly Body eliminates removes the sodium excess fluid “DSR represents a new poten

  19. Slide 19: alfapump DSR

    alfapump DSR® Potential chronic therapy for diuretic-resistant heart failure patients with fluid overload Sodium-free DSR® infusate administered to 1 peritoneal cavity via implanted port 2 Sodium diffuses into DSR infusate 1 alfapump pumps sodium-rich DSR infusate into the 3 bladder Body eliminates

  20. Slide 20: RED DESERT: Study design

    RED DESERT: Study design Repeated dose proof-of-concept study of alfapump DSR® in diuretic-resistant heart failure patients alfapump® + surgical start DSR® therapy discharged from end DSR port implantation in hospital hospital therapy 2 weeks 2 weeks 4 weeks DSR therapy Continued DSR therapy Stabili

  21. Slide 21: Interim RED DESERT: Strong safety & efficacy results

    Interim RED DESERT: Strong safety & efficacy results Results from first five patients SAFETY • Implant procedure of alfapump DSR® and repeated dosing of DSR® therapy were well-tolerated • No clinically significant changes in serum sodium levels / no progressive hyponatremia • Reported adverse events

  22. Slide 22: Interim RED DESERT: Restored normal kidney response

    Interim RED DESERT: Restored normal kidney response Results from first five patients • Diuretic response restored to near normal levels • Sodium excretion more than doubled after DSR study period (to near normal levels) • Long-lasting improvement in diuretic responsiveness • Dramatic reduction in or

  23. Slide 23: Developing high value proprietary DSR Infusate

    Developing high value proprietary DSR® Infusate • D10% was chosen as the initial DSR infusate for fastest proof-of-concept • We are developing our proprietary next-generation DSR infusate:  Improved therapeutic profile compared to D10%  IP protected  Recurring revenue from high gross margin consu

  24. Slide 24: alfapump DSR development strategy

    alfapump DSR® development strategy* Study description 2020 2021 2022 2023 Proof-of-concept repeated dose alfapump DSR study RED DESERT D10% infusate; stable heart failure patients FDA discussions on regulatory pathway alfapump DSR dose-ranging feasibility study** SAHARA D10% infusate; decompensated

  25. Slide 25: Outlook

    Outlook Strong near term value drivers with clear long term potential

  26. Slide 26: Expected core value drivers & outlook

    Expected core value drivers & outlook POSEIDON NASH in North Liver disease / Q4 20: Q1 21: H1 21: Q1 22: America POSEIDON POSEIDON POSEIDON interim analysis 1 enrolment full interim primary endpoint completion analysis read-out Q4 2020 2021 Q1 2022 Heart failure in North America  Q4 20: & Europe H

  27. Slide 27: Thank You

    Thank You  IR@sequanamedical.com  +32 498 053579 www.sequanamedical.com

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