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Does anyone have references or other documentation of pharmaceutical
companies going back to cull more information about their drug from
prior studies (retrospective analysis). For example, a drug may have
been developed to lower LDL cholesterol, and the company may have
gone back to the clinical study data to see if longevity was enhanced
-- or another example, in a PK study on a SR product, a retrospective
analysis was conducted to re-evaluate adverse events. Anecdotal
comments would also be welcomed. Thanks.
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