Standard and reference‐based conditional mean imputation

Author:

Wolbers Marcel1ORCID,Noci Alessandro1,Delmar Paul1,Gower‐Page Craig1,Yiu Sean2,Bartlett Jonathan W.3

Affiliation:

1. Data and Statistical Sciences, Pharma Development Roche Basel Switzerland

2. Data and Statistical Sciences, Pharma Development Roche Welwyn Garden City UK

3. Department of Mathematical Sciences University of Bath Bath UK

Funder

Medical Research Council Canada

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology,Statistics and Probability

Reference27 articles.

1. ICH E9 Working Group.ICH E9 (R1): Addendum on estimands and sensitivity analysis in clinical trials to the guideline on statistical principles for clinical trials;2019.https://database.ich.org/sites/default/files/E9‐R1_Step4_Guideline_2019_1203.pdf. Accessed May 16 2022.

2. Recommendations for the Primary Analysis of Continuous Endpoints in Longitudinal Clinical Trials

3. Aligning Estimators With Estimands in Clinical Trials: Putting the ICH E9(R1) Guidelines Into Practice

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

5. Aligning Treatment Policy Estimands and Estimators—A Simulation Study in Alzheimer’s Disease

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