Please see details below of a PSI one day scientific meeting on Adaptive
Designs: Past, Present and Future on 25th October 2006, 9:30am-4:45pm.
Venue
The Royal Statistical Society
12 Errol Street
London
EC1Y 8LX
This meeting offers presentations from speakers in the area of adaptive
designs, and will include an FDA perspective, comments on the reflections
paper and examples from case studies.
The meeting will be of interest to statisticians who work in the area of
design and analysis of clinical trials.
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09.30 - 10.00 Registration
10.00 - 10.40 An Overview of Interim Analysis and Adaptive Design. Richard
Kay (Consultant)
10.40 - 11.20 Learning vs. Confirming - A Unique Paradigm of Adaptive Design
in Drug Development. Sue Jane Wang (FDA)
11.20 - 11.50 Coffee
11.50 - 12.30 Issues in combining Phase II and Phase III clinical trials.
Chris Jennison (University of Bath)
12.30 - 13.30 Lunch
13.30 - 14.10 Reflections from Industry on the CHMP Reflection Paper on
Confirmatory Clinical Trials with Flexible Design and Analysis Plan. Oliver
Keene (GSK)
14.10 - 14.50 Confirmatory seamless phase II/III clinical trials with dose
selection at interim: General concepts and applications. Frank Bretz (Novartis)
14.50 - 15.20 Coffee
15.20 - 16.00 Application of an Adaptive Sequential Design in a Phase 2/3
Study. Habib Hassani (GSK)
16.00 - 16.45 Closing Address. Andy Grieve (Pfizer)
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Registration Costs
Fee includes lunch & refreshments
Registration before 20th September 2006
PSI Members
£95.00 (plus £16.63 VAT)
Non-Members *
£125.00 (plus £21.88 VAT)
Registration on or after 20th September 2006
PSI Members
£145.00 (plus £25.38 VAT)
Non-Members *
£175.00 (plus £30.63 VAT)
* Price includes affiliate membership for 2006
For further details or a copy of the registration form please contact:
Alison Houghton
Tel: +44 (0)1625 267880 ext 228
Fax: +44 (0)1625 267879
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PSI Executive Office
Resources for Associations
South Park Road, Macclesfield
SK11 6SH, UK
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