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conference details
Conference:
Day one
25 June 8.30am - 5:30pm
Day two
26 June 8.30am - 5:30pm
 
 
Register online for oncology drug development
or call +44 (0) 207 608 7055


Programme


Day one - Wednesday 25 June 2008
Day two - Thursday 26 June 2008

last modified: 18/06/2008 14:31:11 (GMT)

Day one - Wednesday 25 June 2008
8.30am
Registration & coffee
8.50am
Opening remarks from the chair
BUSINESS STRATEGY; KEY DRIVERS AND DEVELOPMENTS

9am
What are the financial sector's expectations for the oncology marketplace?

• market dynamics
• winners and losers
• critical success factors

 
Dr Sapna Srivastava, Vice President,
Morgan Stanley

9.30am
The value of the oncology drugs in development

• Review of recent deals by stages of development
• Is there space in the market for so many new products?
• Reimbursement issues
• Deal valuation

 
Brian Lovatt, Managing Director,
CancerDeals

10am
Pricing for outcome and risk sharing: what are the next steps?
10.30am
Morning tea
11am
Value for money: a European perspective

• Who's values?
• Who's money?
• Who pays?

 
Professor Sir Michael Rawlins, Chairman,
National Institute for Health & Clinical Excellence

11.30am
Are biotech companies prepared to recognise the needs of oncology patients and avoid the mistakes of large pharmaceutical companies?

• How are the issues that impacting today’s medical consumers
• Understanding accomplishments and strides
• How can biotech companies could win the respect of patients
• From the bench to the bedside – translating clinical progress
• Directions in public policy and positive outcomes through collaboration with patient advocates

 
Selma Schimmel, Founder & CEO,
Vital Options International

12pm
Oncology vaccines: should pharmaceutical companies welcome or avoid them?

• Cancer vaccines, tumour types and technologies
• Primary role and synergy with other modalities
• The importance of inhibiting the T-reg and suppressor cell network
• The importance of sequential design and the right drugs in treatment

 
Professor Sir Angus Dalgleish, Foundation Professor of Oncology,
St George's University of London

12.30pm
Lunch
TRANSLATIONAL MEDICINE AND BIOMARKERS

1.30pm
Targeting DNA damage detection and repair pathways to enhance the effectiveness of cancer therapeutics

• Targeted DNA damage detection and repair pathways have become increasingly attractive targets for cancer drug discovery efforts, with several agents now in clinical trials
• Rationale and promise of such agents to provide significant improvements in the treatment of cancer

 
Susan Ashwell, Director, Cancer Chemistry ,
AstraZeneca R&D

2pm
The utility & value of predictive response markers in oncology
 
Dr Hans Winkler, Senior Director, Translational Research ,
Johnson & Johnson

2.30pm
The development of imaging biomarkers for drug development: the potential of molecular imaging

• In-vivo molecular imaging as an emerging discipline to the development of cancer therapies
• New and emerging quantitative functional imaging technology to look at molecular pathways 
• Imaging biomarkers in early clinical trials
• Molecular imaging biomarkers potential to streamline and accelerate rational drug development in oncology

 
Professor Patricia Price, Ralston Paterson Professor of Radiation Oncology ,
Christie Hospital NHS Foundation Trust & University of Manchester

3pm
Afternoon tea
3.30pm
Breakthroughs in cancer biomarker discovery using innovative strategies

• Proteomics technologies; in-depth searches and identification of novel cancer markers
• Discovery research; individual lab effort to collective efforts
• Validation studies and the relevance of novel biomarkers for early cancer detection

 
Dr Samir Hanash, Molecular Diagnostics,
Fred Hutchinson Cancer Research Center, Seattle

4pm
Biomarker Case study
 
Dr Sridhar K Rabindran, Director ,
GlaxoSmithKline Oncology Centre for Excellence in Drug Discovery

4.30pm
Closing Remarks from the chair followed by networking drinks reception
Register Now!

Day two - Thursday 26 June 2008
8.30am
Registration & coffee
8.50am
Opening remarks from the chair
EARLY CLINICAL - As exciting new products enter the clinic and are progressing through the development process, this session will examine the progress of specific products. Special attention will be p


 


9am
Case studies on targeted therapeutics
 
Mr Timothy L Enns, Senior Vice President, Corporate Communications & Business Development,
SuperGen Inc

9.30am
Development of molecular markers for the differential needs of clinical trials and patient diagnostics
 
Dr Joe Monforte, Vice President and Chief Scientific Officer,
Althea Technologies

10am
Targeting the notch pathway
 
Dr Giulio Draetta, Head, Worldwide Basic Oncology Research ,
Merck & Co

10.30am
Improving Timelines of Phase I Dose Finding Studies through Cohort Size Simulations for Anti-Cancer Products
 
Dr Anna Miyamoto,
AstraZeneca

11am
Morning tea
11.30am
Identification & early validation of cancer antibody targets

• target choices: inhibition of cell-surface receptors vs. immune effector targeting
• ligands and receptors: Screening the extracellular proteome for cancer-related functions
• rapid in vivo screening and validation for functionally relevant targets

 
Dr Daniel Pierce, Director of Oncology Discovery,
Five Prime Therapeutics

12pm
Latest clinical results for Novartis' anti-angiogenesis treatment in early stage trials
 
Dr Christian Jacques, Executive Director, Oncology,
Novartis

12.30pm
Amgen's pipeline of targeted therapeutics

• Vectibix; developed for use in patients with advanced stage CRC
• Pivotal trial vs. best supportive care
• Predicting responders which markedly enhanced the benefit: risk ratio
• Pre-specified retrospective analysis in biomarker development
• KRAS in the predictive biomarker field
• KRAS; establishing consistency of hypothesis
• Use of EGFR antagonists

 
Dr Roy Baynes, Vice President, Global Development, Oncology Supportive Care ,
Amgen

1pm
Lunch
REGULATORY UPDATE AND REVIEW - This session will look at specific regulatory challenges that are faced by developers of oncology products it will begin with a broad review of the international arena,

2pm
An Industry Perspective
 
Michael Doherty, Global Head, Pharma Regulatory Affairs,
Hoffman La Roche

2.30pm
The potential impact of recently approved & emerging molecular diagnostics
 
Dr Francis Kalush, Molecular Diagnostics, Office of In Vitro Diagnostics ,
US Food & Drug Administration

3pm
Undertaking head-to-head clinical trials in phase IIb: the commercial and clinical implications of the 505 (b) (2)regulatory pathway to approval
 
Carlo Montagner, President,
Abraxis Oncology

3.30pm
Afternoon tea
NOVEL APPROACHES FOR TARGETED THERAPIES - Targeted therapies are now common place in standard treatment regimens. Many more products are forecast to reach the market over the next few years giving so

4pm
Case study: development of a systems biology designed therapeutic for the treatment of cancer
 
Dr Ulrik B Nielsen, Vice President of Research,
Merrimack Pharmaceuticals

4.30pm
The potential of molecular pathology for targeted therapies
 
Dr Dennis Morgan Smith, Chief Medical Officer,
RedPath Integrated Pathology

5pm
Combination therapies for oncology: targeted challenges
 
Dr Geert Kolvenbag, Executive Director of Development, Emerging Oncology Brands,
AstraZeneca

5pm
Closing remarks and end of conference

 
event partners
Exhibitor:
 
organised by

our speakers
Speaker photo
Professor Sir Michael Rawlins
Chairman
NICE
Speaker photo
Dr Giulio Draetta
Head, Worldwide Basic Oncology Research
Merck & Co
Speaker photo
Dr Christian Jacques
Executive Director, Oncology
Novartis
Speaker photo
Dr Roy Baynes
VP, Global Development, Oncology Supportive Care
Amgen
Speaker photo
Selma Schimmel
Founder & Chief Executive Officer
Vital Options International