Source:http://linkedlifedata.com/resource/pubmed/id/16972710
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2006-9-15
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pubmed:abstractText |
This is a discussion of the following three papers appearing in this special issue on adaptive designs: 'FDA's critical path initiative: A perspective on contributions of biostatistics' by Robert T. O'Neill; 'A regulatory view on adaptive/flexible clinical trial design' by H. M. James Hung, Robert T. O'Neill, Sue-Jane Wang and John Lawrence; and 'Confirmatory clinical trials with an adaptive design' by Armin Koch.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0323-3847
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
48
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
591-7; discussion 613-22
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading | |
pubmed:year |
2006
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pubmed:articleTitle |
Challenges in implementing adaptive designs: comments on the viewpoints expressed by regulatory statisticians.
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pubmed:affiliation |
Novartis Pharmaceuticals, East Hanover, NJ, USA.
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pubmed:publicationType |
Journal Article,
Comment
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