Get exclusive insight from 18 top industry experts including:

  • Gary Acton, Antisoma Gary Acton
    CMO
    Antisoma
  • Prof. Dr. Karol Sikora, CancerPartners UK Prof. Dr. Karol Sikora
    Medical Director
    CancerPartners UK
  • Professor Nicholas Lemoine
    Barts Cancer Institute
    Queen Mary University of London
  • Alun Bedding, GlaxoSmithKline Alun Bedding
    Early Phase Design
    GlaxoSmithKline
  • Maria Orr
    Principal Pharmacogenetics Advisor to Oncology
    AstraZeneca
  • Julian Howell
    Head of Clinical Development
    ProStrakan

Investigating New Trial Design Approaches, Efficient Application of Biomarkers Patient Recruitment Strategies to Drive Oncology Clinical Development and Speed Time to Market

Oncology is undoubtedly the largest investment area for the pharmaceutical industry with latest estimates putting the market at a huge $55 billion. However, there is disparity between this investment in oncology development and the rate of drug approval and there is a drive to bridge this gap through better decision making and optimising clinical development.

Our industry-wide survey has highlighted that the biggest obstacles, yet potential time-savers include;

  • Trial design
  • Implementing biomarkers and functional imaging
  • Patient recruitment and retention strategies
  • Effective use of preclinical data

Do you know what strategies your competitors are implementing over the next 12 months?

Unlocking the potential of alternative trial designs has the power to greatly reduce the time and cost of your trial and speed time to market. With no less than 8 expert-led sessions providing insight into alternative approaches to trial design Pharma IQ's 2nd Annual Optimising Clinical Development in Oncology conference can't be missed!

The event takes place on 15-16 March 2011 in London and is one half of Europe's leading Clinical Trials Summit.

JW McBlane, Clinical Assessor, MHRA will also be giving exclusive insight into the agency's views of the new ICH S9 guidelines. This update will allow you to begin trials on the basis of reduced preclinical data sets and understand what the UK agency deems acceptable, allowing you to minimise your trial time and ensure first time regulatory approval.

Download the brochure here for more details and the full speaker line up.

What the event will discuss:

  • Assessing the possible study design approaches to improve the efficiency of your trial
  • Understanding the correct application of randomised control trials
  • Setting up effective collaborations between pharma and academia to drive innovation
  • Strategies to ensure optimum patient recruitment and build relationships with hospitals and physicians
  • Overcoming the constraints of biomarker development and developing companion diagnostics

Top 7 Reasons to Attend

  • Understand and take home the statistical approach to dose finding
  • Harnessing the potential of personalised medicine through effective patient stratification and DNA sequencing
  • Accurately assessing tumour response based on histological and molecular measurement and enhance biomarker development through implementing functional imaging techniques into clinical development
  • Spearhead innovation and ensure a successful trial through strategic partner selection and effective relationship management. Discuss the value of pharma-academic collaborations and the future of clinical development
  • Ensure first time regulatory approval and speed time to market through implementation of the new ICH S9 guideline - start your clinical trial on reduced preclinical data sets
  • Assessing the importance of patient reported outcomes in the clinical development plan to facilitate partnership formation and pricing and reimbursement
  • Develop long term patient recruitment strategies to improve retention and reduce trial time

Testimonials

I learned a lot at this conference-the topics were interesting.
Janssen
A good mix of functional areas. For training purposes it has been enlightening.
ONO Pharmaceutical UK
Informative, examples from daily practice.
Medigene AG
Sponsor Media Partners
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