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An optimised multi-arm multi-stage clinical trial design for unknown variance
Multi-arm multi-stage trial designs can bring notable gains in efficiency to the drug development process. However, for normally distributed endpoints, the determination of a design typically depends on the assumption that the patient variance in response is known. In practice, this will not usually...
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| Cyhoeddwyd yn: | Contemp Clin Trials |
|---|---|
| Prif Awduron: | , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Elsevier
2018
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5886309/ https://ncbi.nlm.nih.gov/pubmed/29474933 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cct.2018.02.011 |
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