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PERCHERON THERAPEUTICS LIMITED AGM Information 2003

Oct 30, 2003

65543_rns_2003-10-30_df1d137d-fa5d-4325-8f7c-0918c309113e.pdf

AGM Information

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31 October 2003

The Companies Section The Australian Stock Exchange Limited 530 Collins Street MELBOURNE VIC 3000

Dear Sir/Madam

Annual General Meeting 2003 - Presentation Re:

Please find enclosed the presentation to be made to shareholders this morning at Antisense Therapeutics Limited's Annual General Meeting.

Yours sincerely

Natalie Korchev Company Secretary

Overview Corporate Structure Mission/Strategy * Key Achievements Cad Projects - Multiple Sclerosis, Psoriasis * Looking forward * Summary

ense Therarapeutics

  • ♦ Listed on ASX Dec 2001
  • Total funds raised to date: $28.5 M
  • * Market Capitalisation: $43.4 M (undiluted)
  • * Key Shareholders

emae Therapeutres

ense Increases

Z

  • Circadían 20%
  • Syngene 15% (42% Circadian)
  • $Isis$ 11% 5%
  • $-OIC$
  • Cash reserves of $15.4 M, no borrowings

execution and designal

ANP's Mission

Create, develop and commercialize novel antisense pharmaceuticals for large unmet

Business strategy

  • * Leverage 13 years of Isis antisense technology development
  • Fast track existing lead projects through pre-clinical and clinical development
  • * Create pipeline of new antisense therapeutics
  • Commercialise those that are successful in clinical testing via licensing/partnering

Key Achievements - FY 2003

  • * ATL1102 commenced Phase I safety study in humans
  • * ATL1101 completed preclinical efficacy program
  • * Awarded A$1.1M Start Grant
  • ♦ Capital Raising A$15M
  • * Pipeline Undertaken multiple animal studies on antisense compounds for new indications

Multiple Sclerosis - ATL1102

  • * Disease & Market
    • Life-long chronic disease of the central nervous system
    • $-$ Global drug sales of $>$ US$2.5bn in 2002.
    • Need for more effective drug with less side effects

$\bullet$ Product

ense Therapeutics

  • Antisense inhibitor to VLA-4 protein whichcontributes to onset of disease
  • Biogen monoclonal ab to VLA-4 in Phase III
  • Anticipate efficacy, dosing and cost advantages

Multiple Sclerosis - ATL1102 (cont)

♦ Progress

Contraction

Legative Thermeening

  • Confirmed activity in pre-clinical murine models of MS
  • Confirmed activity also in arthritis and asthma models
  • Completed package of pre-clinical animal studies (incl. toxicology)
  • Manufactured drug product for Phase I and IIa studies
  • Commenced Phase I human trial

Multiple Sclerosis - ATL1102 (cont)

♦ Outlook

Controller Control

ense Therapeutics

  • Following successful completion of Phase I trial, Phase IIa trials in 2004

Psoriasis Treatment - ATL1101

* Disease & Market

  • Chronic non-contagious skin disorder
  • Affects 1-2% of population
  • Global drug sales forecaset to exceed US$2 billion by 2007 (Frost & Sullivan)
  • Need for more effective therapies

♦ Product

  • Antisense inhibitor to IGF-IR regulates cell growth - Developing topical formulation

Psoriasis Treatment - ATL1101(cont)

*Progress

  • Selected antisense lead inhibitor
  • Prepared topical formulation
  • Confirmed cream active in psoriasis skin grafts
  • Completed pre-clinical efficacy program
  • Awarded A$1.1 million government grant
  • ♦ Outlook
    • Commence "Proof of Concept" study in psoriasis patients in 2004
Outlook
Project Value Driver Timing
the company ATL1102 Complete Phase I 1st half '64
(MS) +Start Phase IIa 2nd half '04
* Partnering objective Concl Ph Ha
ATL1101(Psoriasis) *Complete product manufactureand toxicology program 1st half '04
*Start "Proof of Concept" study 2 nd half '04
*Partnering objective Concl "PoC"
Pipeline Complete multiple animal Ongoing
Research studies with new antisense leads*Objective: to partner acompound at pre-clinical stage By end 2065

Summary

Antiscotto Therapearics

  • * Significant progress in R&D activities
  • ♦ Strong cash position allowing ANP to reachkey milestones on lead projects
  • ♦ Effective leveraging of partnerships toexpedite R&D programs and reduce development cost and risk
  • Clear commercialisation objectives

High growth potential/reduced technical risk