Zobrazeno 1 - 10
of 81
pro vyhledávání: '"K. J. Pasi"'
Autor:
K. J. Pasi, C Sussebach, Pratima Chowdary, Z Qiu, Margaret V. Ragni, Claude Negrier, S. Andersson, Inga Hegemann, S Poloskey, Pencho Georgiev, B. Mei, Steven W. Pipe, S Kichou, T Lissitchkov
Publikováno v:
65th Annual Meeting of the Society of Thrombosis and Haemostasis Research.
PK-guided personalized prophylaxis with Nuwiq®(human-cl rhFVIII) in adults with severe haemophilia A
Autor:
Pencho Georgiev, Larisa Belyanskaya, Toshko Lissitchkov, Olaf Walter, Sigurd Knaub, Jerzy Windyga, Andreas Tiede, L. Rusen, K. J. Pasi, Liana Gercheva, Johann Bichler, László Nemes, Robert Klamroth
Publikováno v:
Haemophilia. 23:697-704
Introduction Nuwiq® (human-cl rhFVIII) is a 4th generation recombinant human FVIII, without chemical modification or protein fusion, produced in a human cell-line. Aims/Methods This study (NuPreviq) was a prospective, open-label, multicentre, phase
Autor:
Alejandra Ramirez-Santiago, K. J. Pasi, Roshni Kulkarni, Johannes Oldenburg, D. J. Perry, Baisong Mei, Margaret V. Ragni, Tadashi Matsushita, Amy D. Shapiro, Carolyn M. Bennett, Krista Fischer, Beatrice Nolan, Chris Barnes, Johnny Mahlangu, Huixing Yuan, Glenn F. Pierce, Margareth C. Ozelo, Ross I. Baker, G. Allen
Publikováno v:
Thrombosis and Haemostasis. 117:508-518
SummaryThe safety, efficacy, and prolonged half-life of recombinant factor IX Fc fusion protein (rFIXFc) were demonstrated in the Phase 3 B-LONG (adults/adolescents ≥12 years) and Kids B-LONG (children Supplementary Material to this article is avai
Autor:
B. Mei, Claude Negrier, Pencho Georgiev, A.N.L. Prezotti, S. Andersson, K. J. Pasi, K. Salim, Toshko Lissitchkov, Margaret V. Ragni
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss, Pp 74-75 (2020)
Publikováno v:
Journal of Thrombosis and Haemostasis. 14:2141-2147
Essentials No randomized trials have compared long-acting factor VIII (FVIII) with currently used products. A comparison was undertaken using a decision model to predict FVIII use and number of bleeds. In the base case, longer acting FVIII reduced fa
Autor:
Alun Thomas, Elizabeth Chalmers, Savita Rangarajan, Mary Mathias, James S. O’Donnell, K. J. Pasi, Peter William Collins, Pratima Chowdary, David Keeling
Publikováno v:
Haemophilia. 22:487-498
Enhanced half-life factor VIII and IX products are being introduced into routine clinical practice. Published data report on clinical trials and there are limited data available on how to use these products in routine clinical practice. Many patients
Autor:
E. Symington, M. Li, N. Mitchell, G.F. Pierce, W.Y. Wong, B. Madan, C.B. Russell, S. Rangarajan, Margareth C. Ozelo, B. Kim, W. Lester, M. Laffan, K. J. Pasi
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss, Pp 60-(2020)
Autor:
K. J. Pasi, Johnny Mahlangu, Barbara A. Konkle, Simon A Brown, H. Hanabusa, X Li, Savita Rangarajan, G. Allen, Ingrid Pabinger, Lynda M. Cristiano, Beatrice Nolan, D. J. Perry, R. Liesner, Glenn F. Pierce, Guy Young, Shannon Jackson
Publikováno v:
Haemophilia. 22:72-80
Introduction The safety, efficacy and prolonged half-life of recombinant factor VIII Fc fusion protein (rFVIIIFc) in previously treated patients with severe haemophilia A was demonstrated in the phase 3 A-LONG and Kids A-LONG studies. Here, we report
Publikováno v:
Haemophilia. 21:490-495
Introduction Factor XI (FXI) deficiency is the commonest of the rare bleeding disorders, affecting 2079 individuals in the United Kingdom. Treatment options for bleeding or surgery include antifibrinolytics, fresh frozen plasma or plasma-derived (pd)
Autor:
Savita Rangarajan, Daniel P. Hart, B. Palmer, Sean Platton, J. C. Maloney, P. Batty, Gary W. Moore, K. J. Pasi, Louise Bowles
Publikováno v:
Thrombosis and Haemostasis. 114:804-811
SummaryAntibody formation to factor VIII (FVIII) remains the greatest clinical and diagnostic challenge to the haemophilia-treating physician. Current guidance for testing for inhibitory FVIII antibodies (inhibitors) recommends the functional Nijmege