Source:http://linkedlifedata.com/resource/pubmed/id/10567956
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0022671,
umls-concept:C0032659,
umls-concept:C0040223,
umls-concept:C0086045,
umls-concept:C0185125,
umls-concept:C0201734,
umls-concept:C0449864,
umls-concept:C0676831,
umls-concept:C0681842,
umls-concept:C0936012,
umls-concept:C1272706,
umls-concept:C1527178,
umls-concept:C1705938,
umls-concept:C2584321
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pubmed:issue |
2
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pubmed:dateCreated |
1999-12-15
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pubmed:abstractText |
Basiliximab is an immunosuppressant chimeric monoclonal antibody directed to the human interleukin-2 receptor alpha-chain used for prevention of acute rejection episodes in organ transplantation. The minimally effective serum concentration necessary to saturate receptor epitopes in kidney transplant patients is 0.2 microgram/ml. To guide dose selection for Phase 3 efficacy trials, a population pharmacostatistical model was fitted to intensively sampled Phase 2 pharmacokinetic data. This served as a basis from which to examine candidate dose regimens with respect to the duration over which receptor-saturating concentrations would be achieved posttransplant. Three prediction methods were assessed: one based on simulations, and two others based on first-order approximation using either inverse regression or inversion of confidence intervals. An 80% prediction interval was generated by each method to evaluate its predictive performance against prospectively collected Phase 3 data in 39 renal transplant patients who received two injections of 20 mg basiliximab, one prior to surgery and one on Day 4 posttransplant. All methods provided correct prediction of the duration of receptor-saturating concentration. As anticipated, the best performance was obtained from the simulation method which predicted 30 values in the 80% prediction interval, 19.7-52.7 days. The actually observed 80% interval from the Phase 3 data was 23.7-58.3 days.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0090-466X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
27
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
213-30
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pubmed:dateRevised |
2005-11-17
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pubmed:meshHeading |
pubmed-meshheading:10567956-Algorithms,
pubmed-meshheading:10567956-Antibodies, Monoclonal,
pubmed-meshheading:10567956-Calibration,
pubmed-meshheading:10567956-Computer Simulation,
pubmed-meshheading:10567956-Double-Blind Method,
pubmed-meshheading:10567956-Female,
pubmed-meshheading:10567956-Humans,
pubmed-meshheading:10567956-Immunosuppressive Agents,
pubmed-meshheading:10567956-Kidney Transplantation,
pubmed-meshheading:10567956-Male,
pubmed-meshheading:10567956-Middle Aged,
pubmed-meshheading:10567956-Models, Statistical,
pubmed-meshheading:10567956-Nonlinear Dynamics,
pubmed-meshheading:10567956-Population,
pubmed-meshheading:10567956-Predictive Value of Tests,
pubmed-meshheading:10567956-Recombinant Fusion Proteins
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pubmed:year |
1999
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pubmed:articleTitle |
Constructing a prediction interval for time to reach a threshold concentration based on a population pharmacokinetic analysis: an application to basiliximab in renal transplantation.
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pubmed:affiliation |
INSERM U436, Paris, France.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Randomized Controlled Trial,
Clinical Trial, Phase II,
Clinical Trial, Phase III
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