Cynata Therapeutics Limited · ASX:CYP

Cynata Therapeutics — Investor Presentation (June 2018)

24 slides from Cynata Therapeutics's investor presentation, June 2018

  1. Slide 1: A Next Generation Stem Cell Company

    A Next Generation Stem Cell Company Investor Presentation: Cynata Therapeutics Limited June 2018

  2. Slide 2: Important Information

    Important Information This presentation has been prepared by Cynata Therapeutics Limited. (“Cynata” or the “Company”) based on information available to it as at the date of this presentation. The information in this presentation is provided in summary form and does not contain all information necess

  3. Slide 3: Investment Summary: a Phase II-ready biotech with a highly scalable, proprietary platform

    Investment Summary: a Phase II-ready biotech with a highly scalable, proprietary platform for producing commercial quantities of MSCs Scalable, globally ▪ CymerusTM platform enables production of high quality Mesenchymal Stem Cells at scale applicable technology ▪ Fully patented process overcomes mu

  4. Slide 4: Cynata has the only platform in the world to produce commercial quantities of MSCs

    Cynata has the only platform in the world to produce commercial quantities of Mesenchymal Stem Cells from a single source Today’s on-market MSC manufacturing Patented Cymerus Platform solution has a number of shortcomings overcomes shortcomings Sourcing cells from multiple donors leads to ✓ CONSISTE

  5. Slide 5: MSCs are a highly potent form of stem cell attracting significant clinical interest

    MSCs are a highly potent form of stem cell attracting significant clinical interest – and in need of a scalable commercial solution Mesenchymal Stem Cells (MSCs) are believed to play a Global commercial potential, with multiple target vital role in repair and regeneration areas potentially benefitin

  6. Slide 6: Cymerus platform to become the preferred solution for Big Pharma to produce MSCs

    Cynata’s goal is for its patented Cymerus platform to become the preferred solution for Big Pharma to commercially produce MSCs Preclinical data Phase I near completion, Phase II planned ✓Fujifilm licence option ✓Licence available GvHD A ‘hub and spoke’ business model Intention to license Cymerus ac

  7. Slide 7: Trial update | Excellent results in Phase 1 GvHD clinical trial

    Trial update | Excellent results in Phase 1 GvHD clinical trial, a clear validation of Cynata’s MSCs and the Cymerus platform Cynata is nearing completion of a successful Phase 1 clinical trial, demonstrating safety and meaningful impact on the patients’ quality of life ✓ All endpoints achieved to d

  8. Slide 8: Trial update | Substantial improvement in GvHD grades observed

    Trial update | Substantial improvement in GvHD grades observed with the majority of patients reporting a Complete Response Cohort A, lower dose (as at 100-day readout) Cohort B, higher dose (as at 28-day readout) Complete Response rate of 50% Complete Response of 57% 4 4 3 3 GvHD grade GvHD grade 2

  9. Slide 9: Trial update | Response rate represents a meaningful improvement in a $300m market

    Trial update | Response rate represents a meaningful improvement for a life-threatening, severe disease, in a $300m market opportunity1 Trial results to date2 GvHD grade scale3 Substantial improvement in GvHD grade Overall GvHD grade based on a combination of skin, liver and gut stages Skin stage Li

  10. Slide 10: Trial update | Phase 1 GvHD trial designed to demonstrate safety

    Trial update | Phase 1 GvHD trial was designed to demonstrate safety of Cynata’s MSCs and support evaluation of efficacy Graft versus host disease (GVHD) is a condition where following a transplant the donor’s immune cells in the What is transplant (graft) make antibodies against the patient's tissu

  11. Slide 11: Cell therapy is an active market attracting big pharma M&A interest

    Cell therapy is an active market attracting big pharma M&A interest USD USD USD 628M 307M 379M Acquired by Acquired by Acquired by March 2015 February 2016 January 20181 • Enables Fujifilm to combine technologies • Enables Astellas to establish a leading • Extends existing partnership between with C

  12. Slide 12: Cynata is executing on a clear scientific and commercial vision

    Cynata is executing on a clear scientific and commercial vision and continually assesses pathways to maximise shareholder value Fujifilm holds a licence option for development and Multiple options to create commercialisation of Cynata’s MSCs for GvHD shareholder value Exercise of Fujifilm option (US

  13. Slide 13: Cynata intends to demonstrate broad global applicability of its Cymerus platform

    Cynata intends to demonstrate broad global applicability of its Cymerus platform New enhanced pipeline and clear pathway to commercialisation ▪ Direct path to market in Japan following Phase II US$300m1 GvHD ▪ Fujifilm holds a licence option for development and commercialisation of Cynata’s MSCs for

  14. Slide 14: ClearView evaluated the MSC opportunity landscape to identify high priority indications

    ClearView were commissioned to evaluate the full landscape of MSC opportunities to identify high priority indications Indication prioritisation process Cardiovascular disease selected by Cynata ClearView identified as highest priority indication area ~20 high potential target areas Study commissione

  15. Slide 15: New Phase II programme in Critical Limb Ischemia | Opportunity

    New Phase II programme in Critical Limb Ischemia | Opportunity Overview 230,000 ~US$1.4B1 Addressable events per year Forecast annual global market sales Estimated market size Critical Limb ▪ MSC therapy for effective treatment of critical limb ischemia patients who are Ischemia (CLI) ineligible for

  16. Slide 16: Critical Limb Ischemia clinical study follows excellent pre-clinical results

    Critical Limb Ischemia clinical study follows excellent results from an earlier pre-clinical study Mice dosed with Cymerus MSCs experienced significantly improved All results published in a peer outcomes when compared with control group reviewed journal DAY TREATED CONTROL Loss of leg Cytotherapy is

  17. Slide 17: Cynata is well funded to progress its enhanced clinical pipeline

    Cynata is well funded to progress its enhanced clinical pipeline Pre-clinical Phase I Phase II Overview ▪ Excellent results in Phase I GvHD clinical trial: a clear validation of Cynata’s MSCs and the GvHD Phase II ready Cymerus platform ▪ Fujifilm responsible for all further development activities a

  18. Slide 18: Key upcoming milestones

    Key upcoming milestones Today H1 CY2018 H2 CY2018 H1 CY2019 H2 CY2019 Phase I clinical trials If Fujifilm do not exercise their option, Cynata GvHD intends to progress to Phase 2 independently or Cohort B 100 Fujifilm licence with an alternative partner day read-out option expires Detailed trial pla

  19. Slide 19: Cynata will continue to progress pre-clinical studies with leading partners

    Cynata will continue to progress pre-clinical studies with leading academic and commercial partners Pre-clinical Proof of concept Disease target area trials started completed Key highlights Cymerus MSCs demonstrated significant beneficial effects Monash Asthma University ✓ ✓ on three key components

  20. Slide 20: Globally experienced board and management team

    Globally experienced board and management team Dr Paul Wotton Dr Ross Macdonald Dr Stewart Washer Dr John Chiplin Mr Peter Webse Dr Kilian Kelly Chairman Managing Director Chief Non-Executive Director Non-Executive Director Non-Executive Director Vice President, Product Executive Officer Company Sec

  21. Slide 21: Investment Highlights

    Investment Highlights ▪ Scalable, world-first technology: Cymerus platform overcomes inherent challenges of other production methods and enables mass-production of therapeutic MSCs ▪ Phase II ready: Excellent Phase I results provide validation of Cynata’s Cymerus platform; Cynata well positioned to

  22. Slide 22: Appendix | Key recent newsflow: last 6 months

    Appendix | Key recent newsflow: last 6 months Release date Announcement GvHD 21-Jun-18 Positive 28-day data from Cohort B 12-Jun-18 Positive 6-month data from Cohort A 24-May-18 Enrolment completed in Cynata’s Phase 1 Clinical Trial 28-Mar-18 FDA Grants Orphan Drug Designation to Cynata for CYP-001

  23. Slide 23: Appendix | Corporate overview

    Appendix | Corporate overview Company profile Share price performance (last 6 months, A$) 1.60 Cynata Therapeutics is an Australian stock exchange +120% listed clinical-stage biotechnology company developing disruptive regenerative medicines. 1.20 0.80 Financial information +27% Share price (21-June

  24. Slide 24: Thank you for your attention

    Thank you for your attention Cynata Therapeutics Limited Contact details: Level 3 62 Lygon Street ross.macdonald@cynata.com Carlton Victoria 3053 +61 (0) 412 119343 Australia www.cynata.com

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