Reference‐based sensitivity analysis for time‐to‐event data

Author:

Atkinson Andrew12ORCID,Kenward Michael G.3,Clayton Tim1,Carpenter James R.14

Affiliation:

1. Department of Medical StatisticsLondon School of Hygiene and Tropical Medicine London UK

2. Department of Infectious DiseasesBern University Hospital University of Bern, Bern Switzerland

3. Ashkirk Scotland UK

4. MRC Clinical Trials Unit, University College London London UK

Funder

Medical Research Council

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology,Statistics and Probability

Reference54 articles.

1. Panel on Handling Missing Data in Clinical Trials, Committee on National Statistics, Division of Behavioral and Social Sciences and Education;United States National Research Council,2010

2. CHMP.Guidelines on missing data in confirmatory clinical trials. European Medicines Agency download fromhttp://www.ema.europa.eu accessed 15 January 2014.

3. CHMP.Ich e9 (r1) addendum on estimands and sensitvity analysis in clinical trials to the guidance on statistical principles for clinical trials. European Medicines Agency download fromhttp://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2017/08/WC500233916.pdf

4. Adjusting for Nonignorable Drop-Out Using Semiparametric Nonresponse Models

5. Inference in Randomized Studies with Informative Censoring and Discrete Time-to-Event Endpoints

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