Author: Piantadosi, Steven
Title: Highly efficient clinical trial designs for reliable screening of under-performing treatments: Application to the COVID-19 Pandemic. Cord-id: kdhbmsym Document date: 2020_7_15
ID: kdhbmsym
Snippet: BACKGROUND The COVID-19 pandemic presents challenges for clinical trials including urgency, disrupted infrastructure, numerous therapeutic candidates, and the need for highly efficient trial and development designs. This paper presents design components and rationale for constructing highly efficient trials to screen potential COVID-19 treatments. METHODS Key trial design elements useful in this circumstance include futility hypotheses, treatment pooling, reciprocal controls, ranking and selecti
Document: BACKGROUND The COVID-19 pandemic presents challenges for clinical trials including urgency, disrupted infrastructure, numerous therapeutic candidates, and the need for highly efficient trial and development designs. This paper presents design components and rationale for constructing highly efficient trials to screen potential COVID-19 treatments. METHODS Key trial design elements useful in this circumstance include futility hypotheses, treatment pooling, reciprocal controls, ranking and selection, and platform administration. Assuming most of the many candidates for COVID-19 treatment are likely to be ineffective, these components can be combined to facilitate very efficient comparisons of treatments. RESULTS Simulations indicate such designs can reliably discard underperforming treatments using sample size to treatment ratios under 30. CONCLUSIONS Methods to create very efficient clinical trial comparisons of treatments for COVID-19 are available. Such designs might be helpful in the pandemic and should be considered for similar needs in the future.
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