Adalta Ltd. · ASX:1AD

Adalta — Australian Microcap Conference (October 2019)

22 slides from Adalta's conference presentation, October 2019

  1. Slide 1: AdAlta Investor Presentation

    AdAlta Investor Presentation October 2019 Paul MacLeman, Chair Tim Oldham, Chief Executive Officer AdAlta Limited (ASX:1AD)

  2. Slide 2: Disclaimer

    Disclaimer Investment in AdAlta is subject to investment risk, including possible loss of income and capital invested. AdAlta does not guarantee any particular rate of return or performance, nor do they guarantee the repayment of capital. This presentation is not an offer or invitation for subscript

  3. Slide 3: AdAlta overview

    AdAlta overview AdAlta Limited (ASX:1AD) is an Australian listed drug discovery and development company generating a promising new class of protein therapeutics, known as i-bodies, for treating a wide range of human diseases. 3

  4. Slide 4: AdAlta (1AD) investment summary

    AdAlta (1AD) investment summary i-body platform for generating multiple products – Novel structure provides new way to access important biological targets that can be difficult to access with conventional approaches Lead internal program, AD -214 due to commence human Phase 1 clinical trial in early

  5. Slide 5: Financial position

    Financial position Key financial details Share price performance (last 12 months) ASX code 1AD Share price (18 October 2019) AUD$0.13 Market capitalisation AUD$22.18m Ordinary Shares 164,302,007 Listed Options 23,348,803 Unlisted Options 4,355,007 Current cash (30 June 2019)* AUD$5.56m Trading range

  6. Slide 6: AdAlta business model and strategy to create value

    AdAlta business model and strategy to create value 1. In-house Licence to pharma pipeline of drug Revenues: major upfronts + candidates milestones & royalties AD-214 Invest up to key value inflection point i-body i-body drugs technology Long loop that enables new drug class platform and access to no

  7. Slide 7: i-bodies combine benefits of small molecules and conventional antibodies

    i-bodies combine benefits of small molecules and conventional antibodies Long binding loop enables access to Small Conventional AdAlta novel and difficult to Molecule Antibody i-body drug targets High selectivity-specificity Low toxicity: few off target effects Cavity binding and new epitopes Stabil

  8. Slide 8: AdAlta pipeline

    AdAlta pipeline IND Product/ Class of Manufact- Partner Discovery Preclinical enabling Phase I Indication Target Target uring studies AD-214: Idiopathic CXCR4 GPCR Pulmonary Fibrosis AD-214: Other CXCR4 GPCR i-body discovery engine fibrotic indications Novel Not disclosed MCP-1 ligand pocket Ion Not

  9. Slide 9: AD-214 has broad application in treating fibrosis

    AD-214 has broad application in treating fibrosis AdAlta data suggests that AD-214 can improve fibrosis across a range of fibrotic diseases LUNG: Idiopathic Pulmonary Fibrosis EYE: Wet-Age Related Macular Degeneration Lung Eye Liver LIVER: NASH IPF Wet-AMD & PVR NASH & CIRRHOSIS SKIN: Hypertrophic s

  10. Slide 10: AD-214 novel treatment for fibrosis – lung

    AD-214 novel treatment for fibrosis – lung AdAlta’s lead i-body* has demonstrated in vivo activity (reduced collagen content, reduced inflammatory cell infiltration, improved tissue architecture) in a Bleomycin- induced mouse model of lung fibrosis Normal IPF lung tissue IPF lung tissue + AdAlta lun

  11. Slide 11: AD-214 novel treatment for fibrosis – kidney

    AD-214 novel treatment for fibrosis – kidney AdAlta’s lead i-body* has demonstrated in vivo activity (reduced collagen content, improved tissue architecture) in a folic acid-induced mouse model of kidney fibrosis in both preventative and treatment modes Control Folic Acid (FA) FA + neg. i-body FA +

  12. Slide 12: Market opportunity for IPF

    Market opportunity for IPF Idiopathic Pulmonary Fibrosis (IPF) is an irreversible, unpredictable and incurable disease THE STATISTICS People living with IPF 300,000 People die from IPF every year 40,000 Median length of survival after IPF diagnosis 3.8 years 12

  13. Slide 13: AdAlta's place in the IPF treatment landscape

    AdAlta’s place in the IPF treatment landscape Approvals of pirfenidone (2014) and nintedanib (2014) have led to greater confidence in the development of drugs for IPF – Neither are optimal therapies - the disease process is slowed, not reversed A number of products in development – Provide pathway f

  14. Slide 14: AD-214 development: key milestones

    AD-214 development: key milestones 2019 2020 Q3 Q4 Q1 Q2 Q3 Q4 Toxicology studies Clinical study final design and GMP manufacturing Phase I program Bridge Biotherapeutics-BI Adheron-Roche deal done at this stage deal done at this stage 14

  15. Slide 15: GE Healthcare licensing deal – i-body platform

    GE Healthcare licensing deal – i-body platform Overview: Agreement with global medical technology and diagnostics firm, GE Healthcare AdAlta will screen its novel i-body library on a number of targets in order to identify i-bodies that GE can use as imaging agents, starting with Granzyme B Summary o

  16. Slide 16: Market benchmarks

    Market benchmarks Fibrosis Aug-15 right to be acquired by Jul-19 license by Boehringer Sep-15 acquired by Roche BMS Ingelheim €45m + €1.1b lead AD-214 $105m + $475m milestones $150m + $1.25b milestones milestones phase I asset phase IIa asset phase I asset Micro- Feb-18 collaboration with April-16 l

  17. Slide 17: Significant 2019 achievements

    Significant 2019 achievements AD-214 ✓ Successfully completed AD-214 cell-line and manufacturing process development; commenced manufacturing of clinical AD-214 drug substance ✓ Commenced Phase I-enabling non-human primate toxicity studies i-body platform partnerships ✓ Entered partnership with GE H

  18. Slide 18: Expected news flow

    Expected news flow H2 2019 9 Partnership announcement 9 Publication of key i-body data in well recognised, peer reviewed scientific journal, mABs – 4 week NHP toxicology study – to be completed October 2019 – Publication of further key i-body data H1 2020 – Phase I human clinical studies with AD-214

  19. Slide 19: Management focused on milestone delivery

    Management focused on milestone delivery Tim Oldham, PhD CEO & Managing Director Appointed October 2019, Tim brings >20 years of life sciences business development, alliance management, portfolio and product development, and commercialisation experience in Europe, Asia and Australia, with a particul

  20. Slide 20: International Board, Scientific Advisory Board

    International Board, Scientific Advisory Board Extensive track record of drug, antibody development, capital raising and exits Dr Paul MacLeman, Chair Scientific Advisory Board Dr Mick Foley, AdAlta CSO, expert in phage display Dr John Chiplin, Independent Director Liddy McCall, Director Brian Richa

  21. Slide 21: AdAlta Limited (ASX:1AD) Summary

    AdAlta Limited (ASX:1AD) Summary Platform technology for multiple pipeline products and partnerships Lead asset AD-214 – Has significant pre-clinical validation demonstrating broad anti-fibrotic and anti-inflammatory effects as well as safety. – Initial focus on treating Idiopathic Pulmonary Fibrosi

  22. Slide 22: Contact us

    Contact us: Dr Tim Oldham, CEO & Managing Director [email protected] | +61 403 446 665 www.adalta.com.au 22

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