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IMUGENE LIMITED AGM Information 2010

Nov 25, 2010

65124_rns_2010-11-25_2d679b3e-f97e-4a72-a321-355e747f1d70.pdf

AGM Information

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IMUGENE LIMITED Advanced Vaccine Technologies Disease control in pigs and poultry Annual General Meeting 26 November 2010

Dr Warwick Lamb Managing Director

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  • New global license agreement signed

  • top 5 international Animal health company

  • Financial position strengthened by new license deal

  • A$1.75m income to date in 2010/11 year

  • PRRS vaccine development progresses

  • Imugene trial in mid 2010 continues product development

  • Further laboratory based technology improvements

  • Value added to several vaccines

  • Patent portfolio strengthened with new inventions

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Aim: Partner with a firm that brings the global expertise in commercialisation, regulatory approval, sales and marketing Achievements:Agreement with Novartis Animal Health – international industry validation

Benefits:

  • Commercial partners better placed to determine product development, priorities, manufacturing and distribution

  • Work to our company strengths

  • Complements commercial partners development priorities and synergies

  • Economic valuation superior with licensing model – provided deal is the right deal – ours is.

Aim: Product Development - Develop and advance a deep pipeline of products to proof of concept

Achievements:

  • Improved science & patents

  • Proof of concept trials on major products

  • Benefits:

  • Validation of platform

  • Controlled costs of development prior to income generation

  • Clearly defined skill set & commercial strategy

  • Assist global partner

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Imugene

Novartis

  • Technology transfer

  • Fund product development

  • Provide vaccines for trials

  • Designs & perform all trials

  • Expand product pipeline

  • Construct new vaccines

  • Develop commercial scale manufacturing process

  • Manage patent position

  • All regulatory work

  • Modify existing vaccines if required

  • Maximise product range from both platforms

Imugene to be reimbursed for costs

Novartis requires confidentiality on development & terms

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Successful US PRRS trial

  • Evaluated four PRRS vaccine variations

  • Primary candidate performed best

  • Reproduced important findings from Imugene’s 2008 trial

  • Criteria used to evaluate the vaccine are based on those used by USDA for regulatory approval

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2008

2010

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10 12
10
8
8 Control
6
Control T2
6
T2 T3
4
T2 Oral 4 T4
T5
2
2
0 0
Day 42 Day 42
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Lung Lesion Scores

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Cell line for manufacture of all FAV vaccines and the Productivity Enhancer confirmed

  • Improved growth kinetics for PAV vaccines improves yield and reduces cost of goodsPatents lodged and if granted increase PAV vaccine protection until 2028-2030

  • May enable lower dose of PRRS vaccine

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  • Technical and material transfer

  • Liaise and advise on laboratory procedures and animal trial designs

  • Develop new vaccines as required

  • Maintain laboratory capability

  • Patent management

  • Investor relations – Buchan Consulting

  • Analyst briefings commenced

  • Bioshares coverage

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  • International industry validation

  • Large upside from royalties and other fees

  • Spend of < A$10 million to date

  • Income from licensees of over A$4.75 million to date

  • Limited costs moving forward

  • Focussed company responsibilities

  • Products meet demand in large global markets

  • Deep product pipeline

  • Secure patent position

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Directors & management

  - **Graham Dowland – Chairman**

  - **Warwick Lamb – CEO**

  - **Roger Steinepreis – Director**

  - **Mike Sheppard – Chief Scientific Officer**
  • Shares on issue

  • Options (non board)– Mar 11, 20c

143.6 m 3.0 m

  • Ownership:

  • Board, management & their associates

11 %

  • No debt, Minimal overhead, Cash 30 Nov 10 $2.5 m

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