Advancing Clinical Trials in Oncology

Advancing Clinical Trials in Oncology - Event details   08/24/2010 - 08/26/2010 LE MÉRIDIEN CAMBRIDGE, Cambridge, USA  (Massachusetts)   Description Understanding the Effective Design and Execution of Oncology Clinical Trials Key areas being focussed on include: - Reducing attrition rates in oncology drugs in the clinic through better trial design - Incorporating adaptive trial design into oncology trials - Benefits of randomised controlled Phase II trials vs single-arm uncontrolled trials - Importance of the Independent Review - Understanding what constitutes a ‘result’ in patient response - Assessment of clinical endpoints in oncology 1. How to implement the latest FDA guidelines on Progression-Free Survival (PFS) endpoints - Effective Strategies to develop successful companion diagnostics 1. Translating preclinical biomarkers into the clinical setting 2. Trial design strategies to identify biomarker subpopulations during ongoing clinical trials - Challenges and opportunities for global oncology operations - Streamlining operational protocols to identify and remove process bottlenecks 1. Maximising patient recruitment and retention through international collaborative groups 2. Building effective partnerships with CROs and clinical research groups - Improving communication in comparative effectiveness research in clinical trial design 1. Understanding decision critical data for reimbursement appraisals 2. Integration of requirements into effective trial design Category Biotechnology More details (event webpage):  www.hansonwade.com Apply for event:  Link Event language:  English Contact info: Biorbis  Tom Richardson Phone: +44 203 141 8700 Fax: +44 207 222 2685 Email: info@hansonwade.com Contact form:  Link

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