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Autores principales: Meyer, Elias Laurin, Mesenbrink, Peter, Di Prospero, Nicholas A., Pericàs, Juan M., Glimm, Ekkehard, Ratziu, Vlad, Sena, Elena, König, Franz
Formato: Preprint
Publicado: 2022
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Acceso en línea:https://arxiv.org/abs/2210.06228
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author Meyer, Elias Laurin
Mesenbrink, Peter
Di Prospero, Nicholas A.
Pericàs, Juan M.
Glimm, Ekkehard
Ratziu, Vlad
Sena, Elena
König, Franz
author_facet Meyer, Elias Laurin
Mesenbrink, Peter
Di Prospero, Nicholas A.
Pericàs, Juan M.
Glimm, Ekkehard
Ratziu, Vlad
Sena, Elena
König, Franz
contents Non-alcoholic steatohepatitis (NASH) is the progressive form of nonalcoholic fatty liver disease (NAFLD) and a disease with high unmet medical need. Platform trials provide great benefits for sponsors and trial participants in terms of accelerating drug development programs. In this article, we describe some of the activities of the EU-PEARL consortium (EU Patient-cEntric clinicAl tRial pLatforms) regarding the use of platform trials in NASH, in particular the proposed trial design, decision rules and simulation results. For a set of assumptions, we present the results of a simulation study recently discussed with two health authorities and the learnings from these meetings from a trial design perspective. Since the proposed design uses co-primary binary endpoints, we furthermore discuss the different options and practical considerations for simulating correlated binary endpoints.
format Preprint
id arxiv_https___arxiv_org_abs_2210_06228
institution arXiv
publishDate 2022
record_format arxiv
spellingShingle Designing an exploratory phase 2b platform trial in NASH with correlated, co-primary binary endpoints
Meyer, Elias Laurin
Mesenbrink, Peter
Di Prospero, Nicholas A.
Pericàs, Juan M.
Glimm, Ekkehard
Ratziu, Vlad
Sena, Elena
König, Franz
Applications
Non-alcoholic steatohepatitis (NASH) is the progressive form of nonalcoholic fatty liver disease (NAFLD) and a disease with high unmet medical need. Platform trials provide great benefits for sponsors and trial participants in terms of accelerating drug development programs. In this article, we describe some of the activities of the EU-PEARL consortium (EU Patient-cEntric clinicAl tRial pLatforms) regarding the use of platform trials in NASH, in particular the proposed trial design, decision rules and simulation results. For a set of assumptions, we present the results of a simulation study recently discussed with two health authorities and the learnings from these meetings from a trial design perspective. Since the proposed design uses co-primary binary endpoints, we furthermore discuss the different options and practical considerations for simulating correlated binary endpoints.
title Designing an exploratory phase 2b platform trial in NASH with correlated, co-primary binary endpoints
topic Applications
url https://arxiv.org/abs/2210.06228