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our speakers
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Dr Hannah Kettler
Director, Global Health Policy & Advocacy
Bill and Melinda Gates Foundation
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Christian Loucq
Malaria Vaccine Initiative
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Ian Barr
Director
Centre for Influenza
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Dr Jeffrey Ulmer
Global Head of External Research
Novartis
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Dr Ian Frazer
Director
Diamantina Institute for Cancer
conference details
Conference:
Day 1
14th Oct 9am - 5:30pm
Day 2
15th Oct 9am - 5:30pm
 
Workshops: 13th Oct 9am - 5pm
“Practical Application of Risk Management in Vaccine
Compliance and Quality Assurance”
Led by: StephenWilliams, Director, SeerPharma

› Full conference programme
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Register online now
or call +61 2 9021 8808

 

 

 


Programme


Tuesday 14th October 2008
Wednesday 15th October 2008

last modified: 29/08/2008 06:29:07 (GMT)

Tuesday 14th October 2008
8.30am
Registration and welcome coffee
 

8.50am
Opening remarks and welcome from the Chair
Prof Robert Booy, Co-Director, National Centre for
Immunisation Research and Surveillance

A GLOBAL PERSPECTIVE AND LOCAL MARKET OUTLOOK
 

9am
The new era of adjuvant systems
  • Broadening vaccine development beyond antigen research to adjuvanted products
  • A new generation of more powerful adjuvants
  • Identifying the benefits of rapid induction and dose sparing
    capability delivered in pandemics
Dr Su-Peing Ng, Director, Clinical R & D and Medical Affairs Australasia, GlaxoSmithKline

9.25am
The ongoing revolution in global vaccinology
  • Developing global vaccine approaches for global immunisation needs
  • Overcoming the obstacles to the development and global
    distribution of vaccines
  • What does the future hold for international immunisation
    programs?
     
Sir Gustav Nossal, Chair Strategic Advisory Council,
Children’s Vaccine Program, PATH

9.50am
Industry expert panel session: Comparing the Australian market to the global vaccine economy
  • Analysing the local market size, drivers and growth dynamics
  • Which vaccines present the greatest investment opportunities in Australia?
  • Leveraging Australia’s position as a global leader in conducting clinical trials
Andrew Goodsall, Senior Healthcare Analyst, UBS
Rob Gallagher,
Healthcare Analyst, Macquarie Capital

10.30am
Morning tea and Speed Networking
 

OPPORTUNITIES AND CHALLENGES INVACCINE FUNDING
 

11.30am
Supporting global health through sustainable immunisation financing
  • Helping governments secure long-term, sustainable immunisation financing
  • Improving access and increasing R&D through public-private
    partnerships
  • Coordinating sector efforts to stimulate vaccine development
Dr Hannah Kettler, Director Global Health Policy & Advocacy, Gates Foundation

11.55am
Investing in vaccines for developing countries: ethical partnering for profitability
  • Examining the profitability of investing in developing countries
  • Analysing efforts to incentivise the industry
  • Which is the most successful approach?
Dr Mansour Yaich, Vaccine Development Director, PATH

12.20pm
Panel session: Investing in orphan vaccines
  • Why is the industry hesitant to invest in orphan vaccines?
  • Incentivising the development of orphan vaccines
  • Examining legislation designed to overcome the disincentives
    to developing orphan vaccines
     
Dr MansourYaich, Vaccine Development Director, PATH
Dr Hannah Kettler,
Director Global Health Policy & Advocacy, Gates Foundation
Dr Satish Ravetkar,
Senior Director, Serum Institute of India

1pm
Networking lunch
 

GOVERNMENT, POLICY AND REGULATORY ISSUES
 

2pm
National immunisation KOLs panel session: Designing the best national immunisation strategy
  • Reviewing Immunise Australia Program updates
  • Streamlining the process of introducing novel vaccines to
    National Immunisation Schedule
  • Maintaining the high level of public access to vaccines in the
    Australian market
Andrew Pengilley, Medical Advisor, Office of Health Protection, Dept. of Health and Ageing
Assoc Prof Rajiv Khanna,
Director, Australian Centre for Vaccine Development
Prof David Isaacs,
Member, ATAGI and PBAC

2.45pm
Implementing a whole-of-life vaccine registry
  • Why do we need a national adult vaccination registry?
  • Including a vaccine adverse event reporting system in the
    registry
  • Incorporating unique identifiers, a national product catalogue
    and shared e-health records
Karen Gibson, General Manager, National E-Health
Transition Authority

3.10pm
Policy considerations for adult vaccines in Australia
  • Examining the gaps in the Australian National Immunisation Schedule presented by adult vaccines
  • Incorporating boosters and adult vaccines into the Australian
    immunisation strategy
  • Implications of adult vaccines for a whole-of-life registry
Wyeth representative

3.35pm
Introducing a new vaccine to the Australian market
  • Identifying the distinctions of the Australian regulatory landscape
  • Examining the entry challenges faced in Australia
  • Overcoming increasing costs and regulatory complexity
Dr Jane Leong, Medical Director, CSL Biotherapies

4.05pm
Afternoon tea
 

BUILDING PARTNERSHIPS AND EVOLVING BUSINESS MODELS
 

4.30pm
Partnering for success: The vaccine development model
  • How can small biotechs and big pharma work together to produce vaccines quickly and economically?
  • Engaging as a research partner as opposed to a mere investor
  • What is the optimal stage in the development process to
    partner?
Dr Daniel Grant, Head Strategic Alliances ANZ, Pfizer

4.55pm
Adopting a partnership and exchange approach with overseas companies
  • Collaborating with overseas manufacturers to streamline vaccine production
  • How to partner with offshore companies in a technology
    transfer relationship
  • Examining the benefits of importing vaccines in an epidemic
Dr Satish Ravetkar, Senior Director, Serum Institute of India

5.20pm
Biotech innovators panel: Building a successful product portfolio: innovating for future growth
  • Balancing vaccine development portfolios to maximise profitability whilst minimising risk
  • Developing a sustainable R&D pipeline delivering the optimal
    cost-effective vaccines
  • Proactively identifying targets for a global portfolio
     
Dr Andrew O’Brien, MD, BioDiem
Dr Mark Radford, CEO and MD, Symbiosis Group
Dr Martin Soust, MD, SelectVaccines

6pm
End of Day One and networking drinks
 

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Wednesday 15th October 2008
8.30am
Welcome coffee
 

8.50am
Opening remarks and welcome from the Chair
Assoc Prof Rajiv Khanna, Director, Australian Centre for Vaccine Development

THE NEXT GENERATION OFVACCINES
 

9am
Is there a viable future for DNA vaccines?
  • Examining the current state of DNA vaccines
  • Do recent findings spell the end for DNA vaccines?
  • Laying future directions for DNA vaccines research
Dr Jeffrey Ulmer, Global Head of External Research, Novartis

9.30am
Developing a universal influenza vaccine
  • Is a universal influenza vaccine within reach?
  • Reviewing global approaches
  • Examining the latest results from human trials of the M2ebased
    vaccine
Dr Ian Barr, Deputy Director, WHO Centre for Influenza

10am
Therapeutic immunisation: where are we heading?
  • Therapeutic vs. prophylactic vaccines: where does the future of the vaccine market lie?
  • Enhancing responses to multidrug therapy and reducing
    frequency of relapses
  • Therapeutic vaccines for HIV, hepatitis B, malaria,
    tuberculosis and autoimmune diseases
Dr Ian Frazer, Director, Diamantina Institute for Cancer

10.30am
Morning tea
 

AN UPDATE OF GLOBALVACCINE PRIORITIES
 

11am
Examining avian flu pandemic strategies
  • Collaborating between stakeholders to ensure seasonal and pandemic influenza vaccine supply
  • Utilising emerging vaccine technologies to speed up influenza
    vaccine production in a pandemic
  • How ready are we for an avian flu pandemic?
     
Dr Klaus Stohr, Director, Influenza Vaccine Franchises, Novartis

11.25am
Accelerating malaria vaccine development
  • Examining the latest developments in malaria vaccines research
  • Developing a global vaccine approach for a global
    immunisation priority
  • How can public and private sectors work together to
    overcome scientific and economic challenges?
Dr Christian Loucq, Director, PATH MalariaVaccine Initiative

11.50am
Developing a therapeutic Hepatitis C vaccine
  • Examining the latest results from clinical trials: towards a proof-of-concept in patients
  • Including IC41 as an adjuvant in prophylactic Hepatitis
    vaccinations
  • Utilising results to develop a prophylactic Hep C vaccine
Christoph Klade, Vice President Technology Development & Clinical Immunology, Intercell AG

12.15pm
Updating developments in AIDS vaccine research
  • Identifying the most promising vaccines in clinical trials
  • Coordinating R&D efforts across multiple research centres
  • Working together in developing an AIDS vaccine
     
Dr Ian Gust, Chair Scientific Advisory Board, International AIDS Vaccine Initiative

12.40pm
Networking lunch
 

1.40pm
New paradigms and market opportunities in use of novel adjuvants to rejuvenate old vaccines
  • Utilising new adjuvants to protect patents on old vaccines
  • Overcoming the regulatory issues of increased reactogenicity
  • Considering the impact of emerging adjuvants on vaccine
    development
Prof Nikolai Petrovsky, Chairman, Vaxine

DEVELOPMENTS IN DELIVERY SYSTEMS AND ADJUVANTS
 

2.05pm
Examining the benefits of vaccine patch technology
  • Identifying the applications of patch delivery systems: epidemics, travellers and the chronically ill
  • Comparing immune responses elicited by patch vs. traditional
    administration
  • Using patches to deliver otherwise undeliverable adjuvants
Stanley Erck, President and CEO, Iomai Corporation

2.30pm
Investing in mucosal immunisation: the path to product
  • Examining the latest clinical research into mucosal delivery systems
  • Understanding the difficulties in developing a commercially
    viable mucosal immunisation strategy?
  • Identifying which vaccines will be best delivered by mucosal
    routes
Prof Allan Cripps, Pro Vice Chancellor Health, Griffith
University

2.55pm
Afternoon tea
 

STREAMLINING VACCINE PRODUCTION AND DISTRIBUTION FOR THE FUTURE
 

3.20pm
Learning lessons from the EI outbreak: vaccine selection, acquisition, and delivery in an emergency
  • Preparing for emergency outbreaks by ensuring availability
  • Collaborating with manufacturers to ensure steady supply
  • Managing the cold chain for quality and reliability
  • Using a GM product: auditing and training considerations
Ian Denney, Manager Veterinary Services, Animal Health Australia

3.50pm
Innovative technologies to improve vaccine development and production
  • Analysis of traditional development and processing processes
  • Process compression using innovative technologies in
    clarification, ultrafiltration and fluid handling
  • Advances in sterile processing of adjuvant and liposomal
    preparations
  • Increasing regulatory compliance and speeding process
    development using disposable technologies
Michael Payne, Knowledge Development Manager, Millipore

4.15pm
Panel session: Future prospects for the global vaccines market
  • Emerging threats to the global vaccines industry
  • Future of government immunisation legislation
  • Global strategies for the international markets
Dr Hannah Kettler, Director Global Health Policy & Advocacy, Gates Foundation
Dr MansourYaich,
Vaccine Development Director, PATH
Prof Robert Booy,
Co-Director, National Centre for
Immunisation Research and Surveillance
GlaxoSmithKline representative

5pm
Closing remarks and close of conference
 

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