home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
  HUM-MOLGEN -> Events -> Meetings and Conferences

Search

 
  Technology Commercialisation: Developing Biotech Start-Ups  
  February 21, 2001

Biotechnology

 
     
  SMi Pharma, The Hatton, London
21st - 22nd May 2001 plus morning workshop 23rd May


Day One – Monday May 21st 2001

8.30 Registration & Coffee

CHAIRMAN'S OPENING PRESENTATION
9.10 Trends and opportunities: an overview
 Financing trends in the biotech sector
 Creating opportunities in life sciences
 Collaborations: the lifeblood of biotechs
Dimitri F Dimitriou, Senior Director, Worldwide Business Development, GlaxoSmithKline

REVIEWING THE TECHNICAL AND COMMERCIAL ASSESSMENT OF DEVELOPMENT STAGE TECHNOLOGIES
9.40 Focusing on new approaches
 Strategic needs of emerging companies: from set up to launch
 Assessing opportunities and developing strategies for seeking optimum funding
 Assessing scientific innovation vs generating financial forecasts: critique valuation methods
 Developing the need for a technology valuation scoring system
 Understanding the individual needs of various stakeholders
 Developing communication strategies targeted to the different needs of stakeholders
Adam Raman, Director, Strategy Development, PHASE II International

IS YOUR MOLECULE READY TO MARKET OR PARTNER?
10.20 Incorporating marketing objectives into clinical development
 Historically, the pharma and biotech industries have focused on the NDA, not the market, when designing clinical programs
 This myopia often resulted in unnecessary marketing limitations due to an unnecessarily restrictive label
 This presentation will discuss new strategies for evaluating drug candidates and their markets in order to realise a molecule’s full potential either in the market or in a partnering deal
 One or more case studies will be presented
Mark A King, Managing Director, Kendall Strategies

11.00 Morning Coffee

COMMERCIALISING A LEAD CANCER PRODUCT
11.20 Case study: Antigenics
 Developing an integrated infrastructure to develop and commercialise Oncophage®
 Expanding the clinical development programme
 Building a sales force prior to commercialisation
 Creating value through prudent funding strategies
Dr Elma S Hawkins, Vice Chairman, Antigenics

TECHNOLOGY TRANSFER
12.00 The commercialisation process
 Why transfer technology from universities?
 Recognising the commercial implications of academic discoveries
 What are the stages of technology transfer and commercialisation?
 What are the options for technology commercialisation from academia? Established companies, start-ups or spin-offs?
 Bringing science and commercial groups together
Glynn Edwards, Chief Executive Officer, Antisoma

12.40 Networking Lunch

COMMERCIALISING TECHNOLOGY FROM ACADEMIA
2.00 Striding the academic-industrial interface: a personal view
 An industrialist links with academics
 An industrialist joins an academic spin-out
 From spin-out to buy-out
 From buy-out to acquisition to academic chair
 Start-up / spin-out of a service business
 Spin-out of a R&D business
Prof Howard Stevens, Pfizer Professor of Exploratory Drug Delivery, Department of Pharmaceutical Sciences, University of Strathclyde, UK

FROM ACADEMIA TO BIOTECH: A SUCCESS STORY
2.40 Case study: Acambis
 A brief history of Acambis
 From university to biotech: the stages of company development and technology
commercialisation
 Technology platforms for new vaccines
 Commercialising the technology
 Strengthening the financial position through alliances
 Focusing the portfolio
 Maintaining a strategy for constant new product opportunities
Dr John Brown, Chief Executive Officer, Acambis

3.20 Afternoon Tea

TECHNOLOGY TRANSFER: THE HUMAN FACTOR
3.40 From innovation to commercialisation
 Understanding the stages and some of the issues involved
 Working toward speeding up the process from innovation to commercialisation
 What human skills are required for successful technology transfer?
 Finding the right teams
 Integrating the scientific and commercial teams
 Planning for success, some good and bad examples
Cynthia Larbey, Managing Director, People in Health

FROM THE LABORATORY TO THE MARKET-PLACE
4.20 The challenges of commercialising science
 Historical perspective: what motivates scientists?
 The current situation: how do scientists link up with business?
 Geographical comparisons: US vs European culture
 Venture capital, biotechnology companies, big Pharma – an exploration of their different roles
 The future: where will we be in five years time?
Dr Peter MacLennan, Director of Business Development, Pharma-Transfer

5.00 Chairman’s Closing Remarks and Close of Day One

5.10 Networking Drinks Reception



Day Two – Tuesday May 22nd 2001

8.30 Re-registration and Coffee

9.00 Chairman's Opening Remarks
Dr Nigel Parker, Chief Executive Officer, Ark Therapeutics

EARLY STAGE FUNDING
9.10 Raising finance
 Funding options for early stage biotech businesses
 The importance of the right partner for the biotech start-up
 Identifying and evaluating potential partners
 Access to capital and the effect on IP protection
 How can the biotech start-up present themselves to increase their chances of funding and commercialisation?
Antony Ross, Director, Healthcare, 3i Group

RAISING FINANCIAL SUPPORT FOR COMMERCIALISATION
9.40 IPOs and venture capital
 The new issue market and raising funds through initial public offering (IPO)
 Advantages and disadvantages of ‘going public’ for the biotech start-up
 Pros and cons of private placements
 Venture capital financing
 Trends in venture capital financing in the US and Europe
 Qualitative and quantitative analyses of venture capital funding trends
 Advantages and disadvantages
Stephanie Léouzon, Managing Director, Credit Suisse First Boston

COMMERCIALISING A DRUG-DISCOVERY PROCESS IN ANTI-INFECTIVE RESEARCH
10.20 The crucial factors
 World leading science
 Strong management
 Clear business model
 Broad product portfolio
 Supportive investors
Ken Powell, Chief Executive Officer, Arrow Therapeutics

11.00 Morning Coffee

RISK MANAGEMENT AND BARRIERS TO COMMERCIALISATION
11.20 What can be done to minimise risks and overcome barriers?
 Does biotechnology involve such high-risks?
 Understanding barriers
 Understanding risks
 Strategies to overcome barriers and manage risks
 Developing a successful commercialisation strategy acknowledging risk and barriers
Dr Stephen Castle, Managing Director, Mattson Jack Group-Europe

M&A AS A STRATEGY FOR COMMERCIALISATION
12.00 Considerations of scale and attractiveness to capital markets influence current M&A thinking
 Facing the harsh imperative of M&A
 Ambitious business models required for a new era
 Acquisition of critical mass
 Diversification of development risk
 Capabilities versus cash
 Maximising valuation and providing liquidity options to shareholders
Geoff Collett, Vice President, Corporate Development, Lorus Therapeutics

12.40 Networking Lunch

THE IMPACT OF PHARMACOGENOMICS ON DRUG DISCOVERY, DEVELOPMENT AND COMMERCIALISATION
2.00 Transforming potential into value
 Overcoming ‘pharmacogenomicsophobia’
 Attuning drug development to genetic variability
 Targeting blockbusters and eliminating non-responders
 Making pharmacogenomics happen
 Changing the diagnostics paradigm
 Healthcare impact
Dr Bruce L Maloff, Executive Vice President, Commercial Operations, Variagenics

IMPLEMENTING DECISION ANALYSIS IN THE PHARMACEUTICAL ARENA
2.40 Making high quality decisions for drug development
 A brief history of decision analysis (DA) and its application to R&D intensive enterprises
 A review of the application of DA to problems in pharmaceutical development
 How to assess development risk, commercial return and produce high quality decisions
 Case study:
 How DA was implemented at Abbott
 How Abbott uses DA in pharma development
Dr Steven Kuemmerle, Director, Decision Support Group, Abbott Laboratories

3.20 Afternoon Tea

TECHNOLOGY MANAGEMENT
3.40 A new paradigm
 Pharmaceutical market consolidation
 The needs of academia
 The MMI model
 Strategic alliances
 The investor’s view
David Best, Chairman, Medical Marketing International Group

4.20 STRATEGIES, NEED AND IMPACT OF HIGH QUALITY COMBINATORIAL CHEMISTRY ON DRUG DISCOVERY CAPABILITIES OF THE PHARMACEUTICAL
INDUSTRY IN THE POST-GENOMICS ERA
 Augment the internal drug discovery capabilities of pharmaceutical and biopharmaceutical companies
 Broaden and deepen our technology through internal inventions, acquisitions, multiple revenue streams and expand our knowledge base
 Understand what business partners want
 A clear pathway from research ideas to high quality products
 Fully integrated chemistry platform
 Good combinatorial libraries come from good science
Dr Kumar G Gadamasetti, Senior Director, ChemRx Advanced Technologies [Discovery Partners International]

5.00 Chairman's Closing Remarks and Close of Conference

Workshop
MANAGING UNCERTAINTY
In association with Mattson Jack Group-Europe
23rd May 2001

This workshop builds on many of the aspects covered in the preceding conference. Forecast models and valuations are essential in today’s process of commercialisation. A good forecast model will capture the essential elements of the product and market – as it is seen today and how it is perceived to develop over time - taking into consideration changes in the environment at a macro and micro level. Understanding the essential elements enables the practitioner to start managing uncertainty.

This workshop will focus on lessons learnt from over 20 years of technology and product assessments, captured in forecast models – presenting best practice in managing uncertainty. Case studies will be used throughout the workshop - including Monte Carlo analysis, NPV and P&L, epidemiology (research & analysis) and means of generating data to support assumptions via primary and secondary market research.

8.30 Registration and coffee

9.00 Purpose and output of forecasts
Best practice in forecasting
Methods and tools in forecasting

11.00 Morning coffee

11.15 Epidemiology – patient based forecasting
Generating and supporting assumptions
Managing uncertainty

12.30 Discussion and review of session

1.00 Close of session
About your workshop leaders
Nic Talbot-Jenkins joined MJG in 1998 as Senior Analyst and is responsible for forecast modelling for the Group. She has worked on the assessment of many therapy sectors and technologies from early to late stage technology.
Julie Davidson is a qualified epidemiologist trained in both the UK and USA and she is responsible for supporting companies in identifying relevant patient populations.
Stephen Castle has 15 years biotech/pharma industry experience primarily in sales, marketing and business development with in-depth exposure to understanding and managing uncertainty.
 
 
Organized by: Katherine Britton, Deputy Head of Pharma Conferences, SMi
Invited Speakers:  Dimitri F Dimitriou, Senior Director, Worldwide Business Development, GlaxoSmithKline
 Dr Steve Kuemmerle, Director, Decision Support Group, Abbott Laboratories
 Dr John Brown, Chief Executive Officer, Acambis
 Adam Raman, Director, Strategy Development, PHASE II International
 Prof Howard Stevens, Pfizer Professor of Exploratory Drug Delivery, Department of Pharmaceutical Sciences, University of Strathclyde
 Ken Powell, Chief Executive Officer, Arrow Therapeutics
 Cynthia Larbey, Managing Director, People in Health
 Geoff Collett, Vice President, Corporate Development, Lorus Therapeutics
 David Best, Chairman, Medical Marketing International Group
 Dr Bruce L Maloff, Executive Vice President, Commercial Operations, Variagenics
 Dr Elma S Hawkins, Vice Chairman, Antigenics
 Dr Kumar G Gadamasetti, Senior Director, ChemRx Advanced Technologies [Discovery Partners International]
 Mark A King, Managing Director, Kendall Strategies
 Glynn Edwards, Chief Executive Officer, Antisoma
 Dr Stephen Castle, Managing Director, Mattson Jack Group-Europe
 Stephanie Léouzon, Managing Director, Credit Suisse First Boston
 Antony Ross, Director of Healthcare, 3I
 Dr Peter MacLennan, Director of Business Development, Ark Therapeutics

Chaired by:
 Dimitri F Dimitriou, Senior Director, Worldwide Business Development, GlaxoSmithKline
 Dr Nigel Parker, Chief Executive Officer, Ark Therapeutics
 
Deadline for Abstracts: Programme is now full, please come along as a delegate
 
Registration: Register on-line at www.smi-online.co.uk/commercial.asp or phone for a brochure +44 (0) 20 7827 6048
On-the-day registrations welcome.
Price: £1298 Conference plus workshop,
£999 conference only, £399 workshop only.
50% Discount for academics and charities
E-mail: kbritton@smi-online.co.uk
 
  Posted by:   Katherine Britton  
Host: 213.38.112.46
   
 
home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
 
 

Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995-2001 HUM-MOLGEN. All rights reserved. Liability and Copyright.