Practical considerations for optimal designs in clinical dose finding studies

dc.contributor.authorBretz, Frank
dc.contributor.authorDette, Holger
dc.contributor.authorPinheiro, Jose
dc.date.accessioned2009-01-13T07:59:29Z
dc.date.available2009-01-13T07:59:29Z
dc.date.issued2009-01-13T07:59:29Z
dc.description.abstractDetermining an adequate dose level for a drug and, more broadly, characterizing its dose response relationship, are key objectives in the clinical development of any medicinal drug. If the dose is set too high, safety and tolerability problems are likely to result, while selecting too low a dose makes it difficult to establish adequate efficacy in the confirmatory phase, possibly leading to a failed program. Hence, dose finding studies are of critical importance in drug development and need to be planned carefully. In this paper we focus on practical considerations for establishing efficient study designs to estimate target doses of interest. We consider optimal designs for both the estimation of the minimum effective dose (MED) and the dose achieving 100p% of the maximum treatment effect (EDp). These designs are compared with D-optimal designs for a given dose response model. Extensions to robust designs accounting for model uncertainty are also discussed. A case study is used to motivate and illustrate the methods from this paper.en
dc.identifier.urihttp://hdl.handle.net/2003/25988
dc.identifier.urihttp://dx.doi.org/10.17877/DE290R-1955
dc.language.isoende
dc.subjectDose findingen
dc.subjectDose responseen
dc.subjectMinimum effective doseen
dc.subjectModel uncertaintyen
dc.subjectRobust designsen
dc.subjectSample sizeen
dc.subjectTarget dose estimationen
dc.subject.ddc004
dc.titlePractical considerations for optimal designs in clinical dose finding studiesen
dc.typeTextde
dc.type.publicationtypereporten
dcterms.accessRightsopen access

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