Starpharma Holdings Limited · ASX:SPL

Starpharma — Citi's 10th Annual Australian and New Zealand Investment Conference 2018

35 slides from Starpharma's conference presentation, Oct 17, 2018

  1. Slide 1: Starpharma Investor Presentation for Citi Conference

    Starpharma Investor Presentation for Citi Conference Melbourne, Australia; 17 October 2018: Starpharma (ASX: SPL, OTCQX: SPHRY) will today participate in Citi's 10th Annual Australian and New Zealand Investment Conference in Sydney. The invitation-only Citi Conference brings together 65 ASX listed c

  2. Slide 2: Corporate Overview

    Corporate Overview DR JACKIE FAIRLEY CEO October 2018 STARPHARMA HOLDINGS LIMITED ASX:SPL; OTCQX:SPHRY

  3. Slide 3: Important notice and disclaimer

    Important notice and disclaimer This document contains certain forward-looking statements, relating to Starpharma’s business, which can be identified by the use of forward-looking terminology such as “promising”, “plans”, “anticipated”, “will”, “project”, “believe”, “forecast”, “expected”, “estimate

  4. Slide 4: Overview: Deep portfolio of products and extensive partnerships

    Overview: Deep portfolio of products and extensive partnerships with leading companies • Melbourne-based ASX300 company; Market Cap ~A$540M • Unique proprietary polymer (dendrimer) platform • Deep portfolio of products in large, high-value markets • Proven track record of commercialisation across th

  5. Slide 5: Global leader in dendrimer products

    Global leader in dendrimer products – multiple commercial partnerships with leading companies Starpharma’s Dendrimer Platform VivaGel® BV APPROVED VIVAGEL® DEP® SUBMISSION ADVANCED NEGOTIATION APPROVED GRANTED IN THE US VivaGel® Condom World-leading Antibody Drug Conjugate Companies MULTIPLE HIGH VA

  6. Slide 6: Mundipharma licenses Starpharma's VivaGel BV

    Mundipharma licenses Starpharma’s VivaGel® BV Mundipharma has licensed VivaGel® BV for Europe, Russia, CIS, Asia, Middle East, Africa and Latin America, to be marketed as part of the popular BETADINE® Feminine Care portfolio Attractive deal terms including revenue share and milestones  Starpharma r

  7. Slide 7: Recent highlights – VivaGel BV

    Recent highlights – VivaGel® BV Mundipharma licensed VivaGel® BV for Europe, Russia, CIS, and the balance of countries in Latin America for an attractive revenue share, in addition to milestones of up to US$15.5M (A$20.9M) Mundipharma licensed VivaGel® BV for Asia, Middle East, Africa and the majori

  8. Slide 8: Recent highlights – DEP

    Recent highlights – DEP® First patent published for Starpharma’s DEP® dendrimer with AstraZeneca’s Bcl2/xL inhibitors; AZ presented data on its first DEP® oncology candidate, AZD0466, a dual Bcl2/xL inhibitor Commenced DEP® docetaxel phase 2 trial following successful phase 1 results in patients wit

  9. Slide 9: Starpharma's deep pipeline of VivaGel and DEP products

    Starpharma’s deep pipeline of VivaGel® and DEP® products provides exceptional optionality 8

  10. Slide 10: Strong financial position

    Strong financial position FY 2018 FY 2017 Key Financial Data A$M A$M Total revenue and income 5.0 3.6  39% Loss from continuing operations (10.3) (15.2)  32% Profit/(loss) from discontinued operation - 23.4 Sale of Agrochemicals Profit/(loss) for the period (10.3) 8.2 Business in FY17 Net operatin

  11. Slide 11: DEP Portfolio

    @ starpharma DEP® PORTFOLIO py -

  12. Slide 12: Dendrimer Enhanced Products Dual Strategy

    Dendrimer Enhanced Products (DEP®) Dual Strategy Starpharma’s dual DEP® strategy provides technical, IP and financial leverage, as well as increasing commercial opportunities, improving ROI and de-risking development INTERNAL DEP® PARTNERED DEP® • Application to • Application to established drugs pa

  13. Slide 13: Better delivery of drugs through DEP

    Better delivery of drugs through DEP® Starpharma’s DEP® technology: delivering drugs more effectively and in a way that is more patient friendly REDUCED SIDE EFFECTS IMPROVED EFFICACY PATENT LIFE DEP® reduces important DEP® improves anti- Over and above the side effects such as bone cancer efficacy1

  14. Slide 14: AstraZeneca multiproduct licence and further program

    '(3‹ AstraZeneca multiproduct licence and further program – Partnered DEP® momentum building DEP® multiproduct licence  First DEP® candidate, AZD0466: US$126M + royalties  Subsequent DEP® candidates US$93M + royalties  Tiered royalties on net sales on the resultant AstraZeneca DEP® products  Ast

  15. Slide 15: AZ's DEP Bcl2/xL inhibitors

    '(3‹ AZ’s DEP® Bcl2/xL inhibitors: compelling efficacy and synergy in combination DEP® Bcl2/xL plus Rituximab^ results in complete tumour regression This is despite the fact that the human lymphoma model is relatively unresponsive to Rituximab alone. In combination the effect is synergistic. ^Rituxi

  16. Slide 16: AstraZeneca's multiproduct licence 1st candidate AZD0466

    '(3‹ AstraZeneca’s multiproduct licence 1st candidate AZD0466: An exciting novel oncology agent “…the DEP® technology has • Bcl2 is an exciting and enabled us to advance a very clinically validated oncology exciting novel oncology target agent towards the clinic” AZD0466 • Venetoclax (Venclexta), a

  17. Slide 17: Starpharma's DEP pipeline – internal products

    Starpharma’s DEP® pipeline – internal products The optionality with the DEP® platform enables Starpharma to build a deep pipeline of enhanced drugs – a very attractive commercial strategy DEP® docetaxel: Starpharma’s most DEP® irinotecan: DEP® cabazitaxel: advanced DEP® product Improved version Dete

  18. Slide 18: DEP docetaxel: Multiple benefits

    DEP® docetaxel: Multiple benefits Docetaxel (Taxotere®) is a blockbuster Starpharma’s patented DEP® cancer drug with peak global sales docetaxel is an enhanced version of >US$3.1B despite having multiple US docetaxel, designed to reduce side- FDA “Black Box” warnings effects such as neutropenia and

  19. Slide 19: DEP platform: reproducible benefits

    DEP® platform: reproducible benefits Improved Efficacy Reproducible results with many candidates & tumour types Improved Safety Reduced neutropenia/bone marrow toxicities Targeting Tumour Tissue 45-70 x more drug in tumour v original drug Improved PK and Half-Life Longer half life and lower peak (Cm

  20. Slide 20: DEP docetaxel Phase 2 Trial

    DEP® docetaxel Phase 2 Trial Phase 1 Trial complete: n= 27 various solid tumours PHASE 2 STUDY (currently recruiting) • No standard steroid pre-treatment required due to DEP® docetaxel’s detergent-free formulation - unlike Taxotere® • Multi-site trial – 4 UK sites recruiting (Guy’s Hospital London,

  21. Slide 21: DEP cabazitaxel: Multiple benefits

    DEP® cabazitaxel: Multiple benefits About cabazitaxel DEP® cabazitaxel (Jevtana®)  Significantly enhanced  2016 sales efficacy versus Jevtana® approx.US$400M (cabazitaxel) in human (est. US$500M by 2018) breast and prostate cancer models  Primary indication – prostate cancer and in clinical devel

  22. Slide 22: DEP cabazitaxel phase 1/2 trial underway

    DEP® cabazitaxel phase 1 / 2 trial underway • Planning to enrol ~35 patients (solid tumours) • Trial underway at multiple sites, including in the UK at Guy’s Hospital and University College London Hospital (UCLH) – currently recruiting • Phase 1: Open-label, sequential dose-escalation Adaptive phase

  23. Slide 23: DEP irinotecan: out-performance in multiple human tumour models

    DEP® irinotecan: out-performance in multiple human tumour models and advanced preparations for phase 1/2 trial An improved HT-29 (colon) Xenograft version of irinotecan (Camptosar®) – which is primarily used for the P<0.0001 treatment of P<0.0001 advanced colorectal cancer (peak sales US$1.1B). HT-2

  24. Slide 24: DEP irinotecan: complete tumour regression & 100% survival

    DEP® irinotecan: complete tumour regression &100% survival in human pancreatic cancer model • DEP® irinotecan alone showed complete tumour regression and 100% survival in a human pancreatic cancer model • This is compared with only very limited inhibition (and no regression) with standard irinotecan

  25. Slide 25: VivaGel Portfolio

    AS) LifeStyles ‘les VIVAGEL® PORTFOLIO

  26. Slide 26: VivaGel portfolio overview – late stage / commercial assets

    VivaGel® portfolio overview – late stage / commercial assets VivaGel® BV: A breakthrough product for Bacterial Vaginosis (BV) Treatment & Prevention of Recurrent BV (rBV) • Approved in AUS and EU • US FDA New Drug Application accepted for filing for both treatment and prevention of rBV - Fast Track

  27. Slide 27: BV has serious health consequences and significant impact for patients

    BV has serious health consequences and significant impact for patients Bacterial Vaginosis (BV) BV – Major Impact for Patients • Most common vaginal infection • Serious medical consequences worldwide (PID, infertility, miscarriage, increased risk of HIV and other • ~30% women infected in US; up to S

  28. Slide 28: VivaGel BV: A breakthrough therapy for BV

    VivaGel® BV: A breakthrough therapy for BV - a significant unmet medical need “VivaGel® BV is a wonderful product which specifically targets BV bacteria. My patients have called it a ‘life-changing and miraculous treatment’.” Dr Belvia Carter, Ob-Gyn, Memphis, Tennessee. Principal investigator in Vi

  29. Slide 29: VivaGel BV: Two Attractive Commercial Opportunities

    VivaGel® BV: Two Attractive Commercial Opportunities 1 in 3 women Significant unmet will get BV medical need for BV TREATMENT Est. market valued at US$750M p.a. 6 in 10 have recurrent BV No approved therapies for rBV PREVENTION (RECURRENT BV) Est. market valued at US$1B p.a. 28

  30. Slide 30: Independent US Market Research for VivaGel BV

    Independent US Market Research for VivaGel® BV Starpharma commissioned independent market research for VivaGel® BV in the US to inform marketing plans and its licensing discussions for the product Qualitative Research Quantitative Research Detailed Interviews Online Surveys 11 Ob-Gyns 70 Ob-Gyns 7 p

  31. Slide 31: US Physicians conclude that VivaGel BV's Product Profile will be very appealing

    US Physicians conclude that VivaGel® BV’s Product Profile will be very appealing to patients >70% of BV Patients are interested in Top VivaGel® BV attributes to patients a non-antibiotic BV therapy Timeto Time ToResolution Resolutionof Of Odour 74% Odor Efficacy Cure Rate 73% Don't Know, Timeto Time

  32. Slide 32: Positive market research findings for VivaGel BV

    Positive market research findings for VivaGel® BV - from US physicians and payers alike “I would love to try it [VivaGel® BV] “it [VivaGel® BV] is certainly simple enough because it is not an antibiotic.” and the side effect profile is minimal” -US GYN #1 -US GYN #6 “The good news is not having an “

  33. Slide 33: Extensive global licensing for VivaGel BV

    Extensive global licensing for VivaGel® BV 32

  34. Slide 34: Outlook

    Outlook VIVAGEL® DEP® PORTFOLIO PORTFOLIO Progress with DEP® docetaxel & VivaGel® BV US / North American licence DEP® cabazitaxel clinical trials VivaGel® BV launch in Australia, Europe DEP® irinotecan to advance to the clinic & other Mundipharma regions New DEP® candidates selected for further Viva

  35. Slide 35: www.starpharma.com

    @ starpharma www.starpharma.com J

Starpharma Holdings — Citi's 10th Annual Australian and New Zealand Investment Conference 2018 on 6ix