Can We Better Understand the Value of New Medications by Creating Incentives for Better Clinical Trial Design?
CHP/PCOR Research in Progress Seminar
Date and Time
May 16, 2007
1:30 PM - 3:00 PM
Open to the public
No RSVP required
Speaker
Todd H. Wagner - Veterens Affairs; Stanford University
The U.S. Food and Drug Administration (FDA) requires that drug developers show that a new drug is safe and effective prior to the drugs approval for marketing. The least expensive way to assess efficacy involves placebo-controlled trials. However, placebo-controlled trials have been criticized for assigning patients to an unethical treatment, for promoting me-too drugs and for failing to provide information regarding the drugs value relative to existing treatments. In this talk, we discuss the incentives favoring placebo-controlled trials, the problems that placebo-controlled trials create, and potentials ways to reduce these problems.
Location
Health Research & Policy Building
(Redwood Building), Room T138-B
259 Campus Drive
Stanford University
Stanford, CA 94305
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