Impact of trial design on the estimation of drug potency and power in clinical trials of haemophilia with inhibitors-Reference-Cited by-同舟云学术

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Impact of trial design on the estimation of drug potency and power in clinical trials of haemophilia with inhibitors

Published:2018-10 Issue: Volume:123 Page:531-538
ISSN:0928-0987
Container-title:European Journal of Pharmaceutical Sciences
language:en
Short-container-title:European Journal of Pharmaceutical Sciences

Author:

Larsen Malte Selch^ORCID,Juul Rasmus Vestergaard,Kreilgaard Mads^ORCID,Kristensen Annemarie T.,Simonsson Ulrika S.H.

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference37 articles.

1. Randomized comparison of prophylaxis and on-demand regimens with FEIBA NF in the treatment of haemophilia A and B with inhibitors;Antunes;Haemophilia,2014

2. Methods for individualising factor VIII dosing in prophylaxis;Ar;Eur. J. Haematol.,2014

3. NONMEM Users Guides (1989–2009);Beal,2009

4. Limited blood sampling for pharmacokinetic dose tailoring of FVIII in the prophylactic treatment of haemophilia A;Björkman;Haemophilia,2010

5. Haemophilias A and B;Bolton-Maggs;Lancet,2003

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Bayesian approach for a 2 x 2 crossover design with repeated measures: a simulation study;Acta Scientiarum. Technology;2023-11-03

2. Rotational thromboelastometry can predict the probability of bleeding events in a translational rat model of haemophilia A following gene‐based FVIIa prophylaxis;Haemophilia;2019-12-04

3. Use of Alternative Designs and Data Sources for Pediatric Trials;Statistics in Biopharmaceutical Research;2019-10-30

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