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Point estimation for adaptive trial designs I: A methodological review

Recent FDA guidance on adaptive clinical trial designs defines bias as “a systematic tendency for the estimate of treatment effect to deviate from its true value,” and states that it is desirable to obtain and report estimates of treatment effects that reduce or remove this bias. The conventional en...

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Bibliografiske detaljer
Udgivet i:Stat Med
Main Authors: Robertson, David S., Choodari‐Oskooei, Babak, Dimairo, Munya, Flight, Laura, Pallmann, Philip, Jaki, Thomas
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley & Sons, Inc. 2022
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7613995/
https://ncbi.nlm.nih.gov/pubmed/36451173
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/sim.9605
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