Fast tipping point sensitivity analyses in clinical trials with missing continuous outcomes under multiple imputation-Reference-Cited by-同舟云学术

Fast tipping point sensitivity analyses in clinical trials with missing continuous outcomes under multiple imputation

Published:2022-06-02 Issue:6 Volume:32 Page:942-953
ISSN:1054-3406
Container-title:Journal of Biopharmaceutical Statistics
language:en
Short-container-title:Journal of Biopharmaceutical Statistics

Author:

Gorst-Rasmussen Anders¹^ORCID,Tarp-Johansen Mads Jeppe²

Affiliation:

1. Biostatistics Centre of Expertise Novo Nordisk A/S, Denmark

2. Advanced Analytics, Novo Nordisk A/S, Denmark

Funder

reported

Publisher

Informa UK Limited

Subject

Pharmacology (medical),Pharmacology,Statistics and Probability

Link

https://www.tandfonline.com/doi/pdf/10.1080/10543406.2022.2058525

Reference29 articles.

1. 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes—2021

2. PIONEER 1: Randomized Clinical Trial of the Efficacy and Safety of Oral Semaglutide Monotherapy in Comparison With Placebo in Patients With Type 2 Diabetes

3. Sensitivity analysis for clinical trials with missing continuous outcome data using controlled multiple imputation: A practical guide

4. International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (2019). ICH E9 (R1) addendum on estimands and sensitivity analysis in clinical trials to the guideline on statistical principles for clinical trials. Accessed 05 August 2021. https://database.ich.org/sites/default/files/E9-R1_Step4_Guideline_2019_1203.pdf

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