Title
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Pharmacokinetics and safety of ticagrelor in infants and toddlers with sickle cell disease aged <24 months
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Author
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Abstract
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Inhibition of platelet activation may reduce vaso-occlusion rates in patients with sickle cell disease (SCD). In the HESTIA4 (NCT03492931) study, 21 children with SCD received a single oral dose of the antiplatelet agent ticagrelor (0.1 mg/kg <6 months; 0.2 mg/kg >= 6 to <24 months). All patients had measurable ticagrelor plasma concentrations. Ticagrelor and active metabolite (AR-C124910XX) exposure were comparable across all groups (<6 months, >= 6 to <12 months and >= 12 to <24 months). Ticagrelor was well tolerated. Palatability was generally acceptable. These data will be used to enable dose selection for further investigations of ticagrelor efficacy and safety in children with SCD. |
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Language
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English
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Source (journal)
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Pediatric Blood and Cancer. - -
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Publication
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Hoboken
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Wiley
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2021
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ISSN
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1545-5009
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DOI
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10.1002/PBC.28977
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Volume/pages
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68
:5
(2021)
, 5 p.
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Article Reference
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e28977
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ISI
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000621421500001
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Pubmed ID
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33629819
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Medium
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E-only publicatie
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Full text (Publisher's DOI)
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Full text (publisher's version - intranet only)
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