Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/14897
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMallinckrodt, Craig H.-
dc.contributor.authorMOLENBERGHS, Geert-
dc.contributor.authorPersinger, Charles-
dc.contributor.authorRuberg, Stephen J.-
dc.contributor.authorSashegyi, Andreas-
dc.contributor.authorLindborg, Stacy R.-
dc.date.accessioned2013-04-03T09:35:52Z-
dc.date.available2013-04-03T09:35:52Z-
dc.date.issued2012-
dc.identifier.citationJournal of Biopharmaceutical Statistics, 22 (3), p. 596-607-
dc.identifier.issn1054-3406-
dc.identifier.urihttp://hdl.handle.net/1942/14897-
dc.description.abstractImproving proof-of-concept (PoC) studies is a primary lever for improving drug development. Since drug development is often done by institutions that work on multiple drugs simultaneously, the present work focused on optimum choices for rates of false positive (α) and false negative (β) results across a portfolio of PoC studies. Simple examples and a newly derived equation provided conceptual understanding of basic principles regarding optimum choices of α and β in PoC trials. In examples that incorporated realistic development costs and constraints, the levels of α and β that maximized the number of approved drugs and portfolio value varied by scenario. Optimum choices were sensitive to the probability the drug was effective and to the proportion of total investment cost prior to establishing PoC. Results of the present investigation agree with previous research in that it is important to assess optimum levels of α and β. However, the present work also highlighted the need to consider cost structure using realistic input parameters relevant to the question of interest.-
dc.language.isoen-
dc.rights© Taylor & Francis Group, LLC-
dc.subject.otherpower; proof-of-concept; Type I error-
dc.titleA portfolio-based approach to optimize proof-of-concept clinical trials-
dc.typeJournal Contribution-
dc.identifier.epage607-
dc.identifier.issue3-
dc.identifier.spage596-
dc.identifier.volume22-
local.bibliographicCitation.jcatA1-
dc.description.notesReprint Address: Mallinckrodt, C (reprint author) - Eli Lilly & Co, Lilly Corp Ctr, Indianapolis, IN 46285 USA. E-mail Addresses:cmallinc@lilly.com-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1080/10543406.2011.564340-
dc.identifier.isi000304678600011-
item.fulltextWith Fulltext-
item.accessRightsOpen Access-
item.contributorMallinckrodt, Craig H.-
item.contributorMOLENBERGHS, Geert-
item.contributorPersinger, Charles-
item.contributorRuberg, Stephen J.-
item.contributorSashegyi, Andreas-
item.contributorLindborg, Stacy R.-
item.fullcitationMallinckrodt, Craig H.; MOLENBERGHS, Geert; Persinger, Charles; Ruberg, Stephen J.; Sashegyi, Andreas & Lindborg, Stacy R. (2012) A portfolio-based approach to optimize proof-of-concept clinical trials. In: Journal of Biopharmaceutical Statistics, 22 (3), p. 596-607.-
item.validationecoom 2014-
crisitem.journal.issn1054-3406-
crisitem.journal.eissn1520-5711-
Appears in Collections:Research publications
Files in This Item:
File Description SizeFormat 
Portfolio_based_PoC_Optimization_V3.pdfPeer-reviewed author version159.79 kBAdobe PDFView/Open
a.pdf
  Restricted Access
Published version133.82 kBAdobe PDFView/Open    Request a copy
Show simple item record

SCOPUSTM   
Citations

3
checked on Sep 7, 2020

WEB OF SCIENCETM
Citations

5
checked on Aug 3, 2024

Page view(s)

54
checked on Sep 7, 2022

Download(s)

224
checked on Sep 7, 2022

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.