Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/43265
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dc.contributor.authorBarrado, Leandro Garcia-
dc.contributor.authorBURZYKOWSKI, Tomasz-
dc.date.accessioned2024-06-26T06:21:36Z-
dc.date.available2024-06-26T06:21:36Z-
dc.date.issued2024-
dc.date.submitted2024-06-25T14:02:28Z-
dc.identifier.citationPharmaceutical statistics,-
dc.identifier.urihttp://hdl.handle.net/1942/43265-
dc.description.abstractIn randomized clinical trials that use a long-term efficacy endpoint, the follow-up time necessary to observe the endpoint may be substantial. In such trials, an attractive option is to consider an interim analysis based solely on an early outcome that could be used to expedite the evaluation of treatment's efficacy. Garcia Barrado et al. (Pharm Stat. 2022; 21: 209-219) developed a methodology that allows introducing such an early interim analysis for the case when both the early outcome and the long-term endpoint are normally-distributed, continuous variables. We extend the methodology to any combination of the early-outcome and long-term-endpoint types. As an example, we consider the case of a binary outcome and a time-to-event endpoint. We further evaluate the potential gain in operating characteristics (power, expected trial duration, and expected sample size) of a trial with such an interim analysis in function of the properties of the early outcome as a surrogate for the long-term endpoint.-
dc.description.sponsorshipThe research has been partly funded by the Service Public de Wallonie, under the research grant First Entreprice Docteur nr. 8162, jointly awarded to International Drug Development Institute (IDDI) SA and the Université Catholique de Louvain (UCLouvain).-
dc.language.isoen-
dc.publisherWILEY-
dc.rights2024 John Wiley & Sons Ltd.-
dc.subject.otherefficacy stopping-
dc.subject.othergroup-sequential design-
dc.subject.otherinterim analysis-
dc.subject.otherrandomized clinical trial-
dc.subject.othersurrogate endpoint-
dc.titleUsing an early outcome as the sole source of information of interim decisions regarding treatment effect on a long-term endpoint: The non-Gaussian case-
dc.typeJournal Contribution-
local.format.pages11-
local.bibliographicCitation.jcatA1-
dc.description.notesBarrado, LG (corresponding author), Int Drug Dev Inst IDDI, Ave Provinciale 30, B-1340 Louvain La Neuve, Belgium.; Barrado, LG (corresponding author), Louvain Inst Data Anal & Modeling, Inst Stat Biostat & Actuarial Sci ISBA, Louvain La Neuve, Belgium.-
dc.description.notesleandro.garciabarrado@iddi.com-
local.publisher.place111 RIVER ST, HOBOKEN 07030-5774, NJ USA-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.statusEarly view-
dc.identifier.doi10.1002/pst.2398-
dc.identifier.pmid38837876-
dc.identifier.isi001238761300001-
local.provider.typewosris-
local.description.affiliation[Barrado, Leandro Garcia; Burzykowski, Tomasz] Int Drug Dev Inst IDDI, Ave Provinciale 30, B-1340 Louvain La Neuve, Belgium.-
local.description.affiliation[Barrado, Leandro Garcia] Louvain Inst Data Anal & Modeling, Inst Stat Biostat & Actuarial Sci ISBA, Louvain La Neuve, Belgium.-
local.description.affiliation[Burzykowski, Tomasz] Hasselt Univ, Data Sci Inst, I Biostat, Hasselt, Belgium.-
local.uhasselt.internationalno-
item.embargoEndDate2024-12-05-
item.fulltextWith Fulltext-
item.fullcitationBarrado, Leandro Garcia & BURZYKOWSKI, Tomasz (2024) Using an early outcome as the sole source of information of interim decisions regarding treatment effect on a long-term endpoint: The non-Gaussian case. In: Pharmaceutical statistics,.-
item.accessRightsEmbargoed Access-
item.contributorBarrado, Leandro Garcia-
item.contributorBURZYKOWSKI, Tomasz-
crisitem.journal.issn1539-1604-
crisitem.journal.eissn1539-1612-
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