Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/31192
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dc.contributor.authorRatitch, Bohdana-
dc.contributor.authorGoel, Niti-
dc.contributor.authorMallinckrodt, Craig-
dc.contributor.authorBell, James-
dc.contributor.authorBartlett, Jonathan W.-
dc.contributor.authorMOLENBERGHS, Geert-
dc.contributor.authorSingh, Pritibha-
dc.contributor.authorLipkovich, Ilya-
dc.contributor.authorO'Kelly, Michael-
dc.date.accessioned2020-05-22T14:46:58Z-
dc.date.available2020-05-22T14:46:58Z-
dc.date.issued2020-
dc.date.submitted2020-05-04T12:10:58Z-
dc.identifier.citationTherapeutic Innovation and Regulatory Science, 54 (2) , p. 370 -384-
dc.identifier.urihttp://hdl.handle.net/1942/31192-
dc.description.abstractThis paper provides examples of defining estimands in real-world scenarios following ICH E9(R1) guidelines. Detailed discussions on choosing the estimands and estimators can be found in our companion papers. Three scenarios of increasing complexity are illustrated. The first example is a proof-of-concept trial in major depressive disorder where the estimand is chosen to support the sponsor decision on whether to continue development. The second and third examples are confirmatory trials in severe asthma and rheumatoid arthritis respectively. We discuss the intercurrent events expected during each trial and how they can be handled so as to be consistent with the study objectives. The estimands discussed in these examples are not the only acceptable choices for their respective scenarios. The intent is to illustrate the key concepts rather than focus on specific choices. Emphasis is placed on following a study development process where estimands link the study objectives with data collection and analysis in a coherent manner, thereby avoiding disconnect between objectives, estimands, and analyses.-
dc.description.sponsorshipDIA Scientific Working Group on Missing Data and the authors’ respective employers.-
dc.language.isoen-
dc.publisherSPRINGER HEIDELBERG-
dc.rights2020 Springer Nature Switzerland AG. Part of Springer Nature.-
dc.subject.otherestimands-
dc.subject.otherclinical trials-
dc.subject.otherintercurrent events-
dc.titleDefining Efficacy Estimands in Clinical Trials: Examples Illustrating ICH E9(R1) Guidelines-
dc.typeJournal Contribution-
dc.identifier.epage384-
dc.identifier.issue2-
dc.identifier.spage370-
dc.identifier.volume54-
local.format.pages15-
local.bibliographicCitation.jcatA1-
dc.description.notesO'Kelly, M (reprint author), IQVIA, Estuary House,East Point Business Pk, Dublin 3, Ireland.-
dc.description.notesMichael.OKelly@iqvia.com-
dc.description.otherO'Kelly, M (reprint author), IQVIA, Estuary House,East Point Business Pk, Dublin 3, Ireland. Michael.OKelly@iqvia.com-
local.publisher.placeTIERGARTENSTRASSE 17, D-69121 HEIDELBERG, GERMANY-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.source.typeArticle-
dc.identifier.doi10.1007/s43441-019-00065-7-
dc.identifier.pmid32072586-
dc.identifier.isiWOS:000522455300014-
dc.identifier.eissn2168-4804-
local.provider.typewosris-
local.uhasselt.uhpubyes-
local.uhasselt.internationalyes-
item.validationecoom 2021-
item.contributorRatitch, Bohdana-
item.contributorGoel, Niti-
item.contributorMallinckrodt, Craig-
item.contributorBell, James-
item.contributorBartlett, Jonathan W.-
item.contributorMOLENBERGHS, Geert-
item.contributorSingh, Pritibha-
item.contributorLipkovich, Ilya-
item.contributorO'Kelly, Michael-
item.fulltextWith Fulltext-
item.accessRightsRestricted Access-
item.fullcitationRatitch, Bohdana; Goel, Niti; Mallinckrodt, Craig; Bell, James; Bartlett, Jonathan W.; MOLENBERGHS, Geert; Singh, Pritibha; Lipkovich, Ilya & O'Kelly, Michael (2020) Defining Efficacy Estimands in Clinical Trials: Examples Illustrating ICH E9(R1) Guidelines. In: Therapeutic Innovation and Regulatory Science, 54 (2) , p. 370 -384.-
crisitem.journal.issn2168-4790-
crisitem.journal.eissn2168-4804-
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