Journal article
Exploratory evaluation of pharmacodynamics, pharmacokinetics and safety of rivaroxaban in children and adolescents: An EINSTEIN-Jr phase i study
D Kubitza, S Willmann, M Becka, K Thelen, G Young, LR Brandão, P Monagle, C Male, A Chan, G Kennet, I Martinelli, P Saracco, AWA Lensing
Thrombosis Journal | BMC | Published : 2018
Abstract
Background: The EINSTEIN-Jr program will evaluate rivaroxaban for the treatment of venous thromboembolism (VTE) in children, targeting exposures similar to the 20 mg once-daily dose for adults. Methods: This was a multinational, single-dose, open-label, phase I study to describe the pharmacodynamics (PD), pharmacokinetics (PK) and safety of a single bodyweight-adjusted rivaroxaban dose in children aged 0.5-18 years. Children who had completed treatment for a venous thromboembolic event were enrolled into four age groups (0.5-2 years, 2-6 years, 6-12 years and 12-18 years) receiving rivaroxaban doses equivalent to 10 mg or 20 mg (either as a tablet or oral suspension). Blood samples for PK an..
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Funding Acknowledgements
The study was funded by Bayer AG and Janssen Scientific Affairs, LLC.