Recombinant factor VIIa analog (vatreptacog alfa [activated]) for treatment of joint bleeds in hemophilia patients with inhibitors: A randomized controlled trial
Summary. Background:A recombinant factor VIIa analog (NN1731; vatreptacog alfa [activated]) was developed to provide safe, rapid and sustained resolution of bleeds in patients with hemophilia and inhibitors. Patients/Methods:This global, prospective, randomized, double-blinded, active-controlled, do...
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th-mahidol.151212018-06-11T12:20:37Z Recombinant factor VIIa analog (vatreptacog alfa [activated]) for treatment of joint bleeds in hemophilia patients with inhibitors: A randomized controlled trial Erich V. de Paula Kaan Kavakli Johnny Mahlangu Yasmin Ayob Steven R. Lentz Massimo Morfini László Nemes Silva Z. Šalek Midori Shima Jerzy Windyga Silke Ehrenforth Ampaiwan Chuansumrit Universidade Estadual de Campinas Ege University Medical School Academic Hospital National Blood Center University of Iowa Azienda Ospedaliera Careggi National Hemophilia Center University of Zagreb School of Medicine Nara Kenritsu Ika Daigaku Fozuku Byoin Institute of Haematology and Transfusion Medicine, Warsaw Novo Nordisk AS Mahidol University Medicine Summary. Background:A recombinant factor VIIa analog (NN1731; vatreptacog alfa [activated]) was developed to provide safe, rapid and sustained resolution of bleeds in patients with hemophilia and inhibitors. Patients/Methods:This global, prospective, randomized, double-blinded, active-controlled, dose-escalation trial evaluated and compared one to three doses of vatreptacog alfa at 5, 10, 20, 40, and 80μgkg -1 with one to three doses of recombinant FVIIa (rFVIIa) at 90μgkg -1 in the treatment of acute joint bleeds in hemophilia patients with inhibitors. The primary endpoint comprised adverse events; secondary endpoints were evaluations of immunogenicity, pharmacokinetics, and efficacy. Results and Conclusions:Overall, 96 joint bleeds in 51 patients ( > 12 years of age) were dosed. Vatreptacog alfa was well tolerated, with a low frequency of adverse events. No immunogenic or thrombotic events related to vatreptacog alfa were reported. A high efficacy rate of vatreptacog alfa in controlling acute joint bleeds was observed; 98% of bleeds were controlled within 9h of the initial dose in a combined evaluation of 20-80μgkg -1 vatreptacog alfa. The efficacy rate observed for rFVIIa (90%) is consistent with data from published clinical trials. The trial was not powered to compare efficacy, and further trials are needed to investigate the efficacy of vatreptacog alfa as compared with that of rFVIIa. The trial was registered at ClinicalTrials.gov (Registration Number: NCT00486278). © 2011 International Society on Thrombosis and Haemostasis. 2018-06-11T05:20:37Z 2018-06-11T05:20:37Z 2012-01-01 Article Journal of Thrombosis and Haemostasis. Vol.10, No.1 (2012), 81-89 10.1111/j.1538-7836.2011.04549.x 15387836 15387933 2-s2.0-84855374941 https://repository.li.mahidol.ac.th/handle/123456789/15121 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84855374941&origin=inward |
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Medicine Erich V. de Paula Kaan Kavakli Johnny Mahlangu Yasmin Ayob Steven R. Lentz Massimo Morfini László Nemes Silva Z. Šalek Midori Shima Jerzy Windyga Silke Ehrenforth Ampaiwan Chuansumrit Recombinant factor VIIa analog (vatreptacog alfa [activated]) for treatment of joint bleeds in hemophilia patients with inhibitors: A randomized controlled trial |
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Summary. Background:A recombinant factor VIIa analog (NN1731; vatreptacog alfa [activated]) was developed to provide safe, rapid and sustained resolution of bleeds in patients with hemophilia and inhibitors. Patients/Methods:This global, prospective, randomized, double-blinded, active-controlled, dose-escalation trial evaluated and compared one to three doses of vatreptacog alfa at 5, 10, 20, 40, and 80μgkg -1 with one to three doses of recombinant FVIIa (rFVIIa) at 90μgkg -1 in the treatment of acute joint bleeds in hemophilia patients with inhibitors. The primary endpoint comprised adverse events; secondary endpoints were evaluations of immunogenicity, pharmacokinetics, and efficacy. Results and Conclusions:Overall, 96 joint bleeds in 51 patients ( > 12 years of age) were dosed. Vatreptacog alfa was well tolerated, with a low frequency of adverse events. No immunogenic or thrombotic events related to vatreptacog alfa were reported. A high efficacy rate of vatreptacog alfa in controlling acute joint bleeds was observed; 98% of bleeds were controlled within 9h of the initial dose in a combined evaluation of 20-80μgkg -1 vatreptacog alfa. The efficacy rate observed for rFVIIa (90%) is consistent with data from published clinical trials. The trial was not powered to compare efficacy, and further trials are needed to investigate the efficacy of vatreptacog alfa as compared with that of rFVIIa. The trial was registered at ClinicalTrials.gov (Registration Number: NCT00486278). © 2011 International Society on Thrombosis and Haemostasis. |
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Universidade Estadual de Campinas |
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Universidade Estadual de Campinas Erich V. de Paula Kaan Kavakli Johnny Mahlangu Yasmin Ayob Steven R. Lentz Massimo Morfini László Nemes Silva Z. Šalek Midori Shima Jerzy Windyga Silke Ehrenforth Ampaiwan Chuansumrit |
format |
Article |
author |
Erich V. de Paula Kaan Kavakli Johnny Mahlangu Yasmin Ayob Steven R. Lentz Massimo Morfini László Nemes Silva Z. Šalek Midori Shima Jerzy Windyga Silke Ehrenforth Ampaiwan Chuansumrit |
author_sort |
Erich V. de Paula |
title |
Recombinant factor VIIa analog (vatreptacog alfa [activated]) for treatment of joint bleeds in hemophilia patients with inhibitors: A randomized controlled trial |
title_short |
Recombinant factor VIIa analog (vatreptacog alfa [activated]) for treatment of joint bleeds in hemophilia patients with inhibitors: A randomized controlled trial |
title_full |
Recombinant factor VIIa analog (vatreptacog alfa [activated]) for treatment of joint bleeds in hemophilia patients with inhibitors: A randomized controlled trial |
title_fullStr |
Recombinant factor VIIa analog (vatreptacog alfa [activated]) for treatment of joint bleeds in hemophilia patients with inhibitors: A randomized controlled trial |
title_full_unstemmed |
Recombinant factor VIIa analog (vatreptacog alfa [activated]) for treatment of joint bleeds in hemophilia patients with inhibitors: A randomized controlled trial |
title_sort |
recombinant factor viia analog (vatreptacog alfa [activated]) for treatment of joint bleeds in hemophilia patients with inhibitors: a randomized controlled trial |
publishDate |
2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/15121 |
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1763491545431932928 |