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Efgartigimod for primary immune thrombocytopenia: the ADVANCE IV trial – Authors' reply
Additionally, although we recognise the potential ability of neonatal Fc receptor inhibitors to modulate fetal and neonatal alloimmune disease resulting from parental red cell or platelet incompatibility, formal and careful studies are needed to evaluate the safety and efficacy of this approach. Ide...
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Published in: | The Lancet (British edition) 2024-08, Vol.404 (10451), p.434-434 |
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creator | Al-Samkari, Hanny B Bussel, James Miyakawa, Yoshi Broome, Catherine M |
description | Additionally, although we recognise the potential ability of neonatal Fc receptor inhibitors to modulate fetal and neonatal alloimmune disease resulting from parental red cell or platelet incompatibility, formal and careful studies are needed to evaluate the safety and efficacy of this approach. Ideally, advances in testing will reliably allow additional such evaluations in the future to better evaluate the mechanism of treatment effect and potentially allow for the establishment of laboratory profiles that predict response. JBB reports honoraria from Novartis, Sobi, Alpine, UCB, argenx, Janssen, and RallyBio; and unpaid leadership roles in a board, society, or advocacy group with Platelet Disorder Society of America, Children's Cancer and Blood Foundation, and Foundation for Women and Girls with Blood Disorders. |
doi_str_mv | 10.1016/S0140-6736(24)01263-7 |
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subjects | Blood Blood platelets Children Clinical trials Fc receptors Fetuses Humans Idiopathic thrombocytopenic purpura Incompatibility Laboratories Neonates Platelets Purpura, Thrombocytopenic, Idiopathic - drug therapy Quality of life Randomized Controlled Trials as Topic Research funding Thrombocytopenia |
title | Efgartigimod for primary immune thrombocytopenia: the ADVANCE IV trial – Authors' reply |
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