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Noninferiority Trial Designs: Perspectives from Academia, Industry, and a Regulatory Agency
Program Code:
258
Date:
Tuesday, June 26, 2012
Time:
1:30 PM to 3:00 PM
EST
CHAIR
:
Weishi Yuan, FDA, United States
PRESENTER
(S):
Brent Logan, Medical College of Wisconsin, United States
Kevin Carroll is currently Chief Statistician at AZ pharmaceuticals, where he is accountable for statistical strategy, input and oversight across all therapeutic development areas. Kevin has published on a wide range of statistical topics including non-inferiority trials and CV outcomes trials.
|
Rajeshwari Sridhara, FDA, United States
Description
There are more clinical trials done using noninferiority design in recent years. In this session, we have invited experts from these three fields to discuss their perspectives on noninferiority designs, method, and experiences.
Learning Objectives:
Define noninferiority (NI) trials
Interpret NI trial outcome
Identify issues involved in NI trial.