Empirical evaluation of the implementation of the EMA guideline on missing data in confirmatory clinical trials: Specification of mixed models for longitudinal data in study protocols-Reference-Cited by-同舟云学术

Empirical evaluation of the implementation of the EMA guideline on missing data in confirmatory clinical trials: Specification of mixed models for longitudinal data in study protocols

Published:2019-07-03 Issue:6 Volume:18 Page:636-644
ISSN:1539-1604
Container-title:Pharmaceutical Statistics
language:en
Short-container-title:Pharmaceutical Statistics

Author:

Häckl Sebastian¹,Koch Armin¹^ORCID,Lasch Florian¹^ORCID

Affiliation:

1. Institute of BiostatisticsHannover Medical School Hannover Germany

Funder

Medizinischen Hochschule Hannover

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology,Statistics and Probability

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pst.1964

Reference28 articles.

1. International Conference on Harmonisation (ICH).Statistical principles for clinical trials (ICH E9);1998.

2. European Medicines Agency (EMA).ICH E9 (R1) addendum on estimands and sensitivity analysis in clinical trials to the guideline on statistical principles for clinical trials—step 2b.2017;44(August):1–23.

3. European Medicines Agency (EMA).Guideline on missing data in confirmatory clinical trials.2011;1–12.

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