메뉴 건너뛰기




Volumn 19, Issue 3, 2013, Pages 344-348

Evolution of the European guidelines for the clinical development of factor VIII products: Little progress towards improved patient management

Author keywords

Clinical trial guidelines; Factor VIII; Factor VIII inhibitors; Haemophilia A; Safety

Indexed keywords

BLOOD CLOTTING FACTOR 8 DERIVATIVE; BLOOD CLOTTING FACTOR 8 INHIBITOR; RECOMBINANT BLOOD CLOTTING FACTOR 8;

EID: 84876801691     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/hae.12041     Document Type: Review
Times cited : (9)

References (15)
  • 1
    • 33645998423 scopus 로고    scopus 로고
    • Mortality and causes of death in patients with hemophilia, 1992-2001: a prospective cohort study
    • Plug I, Van DerBom JG, Peters M et al. Mortality and causes of death in patients with hemophilia, 1992-2001: a prospective cohort study. J Thromb Haemost 2006; 4: 510-6.
    • (2006) J Thromb Haemost , vol.4 , pp. 510-516
    • Plug, I.1    Van Der Bom, J.G.2    Peters, M.3
  • 2
    • 77953549604 scopus 로고    scopus 로고
    • Mortality and causes of death in Italian persons with haemophilia, 1990-2007
    • Tagliaferri A, Rivolta GF, Iorio A et al. Mortality and causes of death in Italian persons with haemophilia, 1990-2007. Haemophilia 2010; 16: 437-46.
    • (2010) Haemophilia , vol.16 , pp. 437-446
    • Tagliaferri, A.1    Rivolta, G.F.2    Iorio, A.3
  • 3
    • 0023856830 scopus 로고
    • The natural history of factor VIII:C inhibitors in patients with hemophilia A: a national cooperative study. II. Observations on the initial development of factor VIII:C inhibitors
    • McMillan CW, Shapiro SS, Whitehurst D, Hoyer LW, Rao AV, Lazerson J. The natural history of factor VIII:C inhibitors in patients with hemophilia A: a national cooperative study. II. Observations on the initial development of factor VIII:C inhibitors. Blood 1988; 71: 344-8.
    • (1988) Blood , vol.71 , pp. 344-348
    • McMillan, C.W.1    Shapiro, S.S.2    Whitehurst, D.3    Hoyer, L.W.4    Rao, A.V.5    Lazerson, J.6
  • 4
    • 33751017721 scopus 로고    scopus 로고
    • Incidence of inhibitors in a cohort of 838 males with hemophilia A previously treated with factor VIII concentrates
    • Kempton CL, Soucie JM, Abshire TC. Incidence of inhibitors in a cohort of 838 males with hemophilia A previously treated with factor VIII concentrates. J Thromb Haemost 2006; 4: 2576-81.
    • (2006) J Thromb Haemost , vol.4 , pp. 2576-2581
    • Kempton, C.L.1    Soucie, J.M.2    Abshire, T.C.3
  • 5
    • 79959486802 scopus 로고    scopus 로고
    • Incidence of factor VIII inhibitors throughout life in severe hemophilia A in the United Kingdom
    • Hay CR, Palmer B, Chalmers E et al. Incidence of factor VIII inhibitors throughout life in severe hemophilia A in the United Kingdom. Blood 2011; 117: 6367-70.
    • (2011) Blood , vol.117 , pp. 6367-6370
    • Hay, C.R.1    Palmer, B.2    Chalmers, E.3
  • 6
    • 0027392864 scopus 로고
    • A higher than expected incidence of factor VIII inhibitors in multitransfused haemophilia A patients treated with an intermediate purity pasteurized factor VIII concentrate
    • Peerlinck K, Arnout J, Gilles JG, Saint-Remy JM, Vermylen J. A higher than expected incidence of factor VIII inhibitors in multitransfused haemophilia A patients treated with an intermediate purity pasteurized factor VIII concentrate. Thromb Haemost 1993; 69: 115-8.
    • (1993) Thromb Haemost , vol.69 , pp. 115-118
    • Peerlinck, K.1    Arnout, J.2    Gilles, J.G.3    Saint-Remy, J.M.4    Vermylen, J.5
  • 7
    • 0027394923 scopus 로고
    • A sudden increase in factor VIII inhibitor development in multitransfused hemophilia A patients in The Netherlands. Dutch Hemophilia Study Group
    • Rosendaal FR, Nieuwenhuis HK, Van DenBerg HM et al. A sudden increase in factor VIII inhibitor development in multitransfused hemophilia A patients in The Netherlands. Dutch Hemophilia Study Group. Blood 1993; 81: 2180-6.
    • (1993) Blood , vol.81 , pp. 2180-2186
    • Rosendaal, F.R.1    Nieuwenhuis, H.K.2    Van Den Berg, H.M.3
  • 8
    • 0037415123 scopus 로고    scopus 로고
    • Blood safety monitoring among persons with bleeding disorders-United States. May 1998-June 2002
    • Blood safety monitoring among persons with bleeding disorders-United States. May 1998-June 2002. MMWR Morb Mortal Wkly Rep 2003; 51: 1152-4.
    • (2003) MMWR Morb Mortal Wkly Rep , vol.51 , pp. 1152-1154
  • 9
    • 0029617930 scopus 로고
    • Haemophilia A: mutation type determines risk of inhibitor formation
    • Schwaab R, Brackmann HH, Meyer C et al. Haemophilia A: mutation type determines risk of inhibitor formation. Thromb Haemost 1995; 74: 1402-6.
    • (1995) Thromb Haemost , vol.74 , pp. 1402-1406
    • Schwaab, R.1    Brackmann, H.H.2    Meyer, C.3
  • 10
    • 0032854688 scopus 로고    scopus 로고
    • Malmo International Brother Study (MIBS): an international survey of brother pairs with haemophilia
    • Astermark J, Berntorp E. Malmo International Brother Study (MIBS): an international survey of brother pairs with haemophilia. Vox Sang 1999; 77(Suppl 1): 80-2.
    • (1999) Vox Sang , vol.77 , Issue.SUPPL 1 , pp. 80-82
    • Astermark, J.1    Berntorp, E.2
  • 11
    • 0031598278 scopus 로고    scopus 로고
    • Inhibitors occur more frequently in African-American and Latino haemophiliacs
    • Aledort LM, Dimichele DM. Inhibitors occur more frequently in African-American and Latino haemophiliacs. Haemophilia 1998; 4: 68.
    • (1998) Haemophilia , vol.4 , pp. 68
    • Aledort, L.M.1    Dimichele, D.M.2
  • 12
    • 0031045680 scopus 로고    scopus 로고
    • HLA genotype of patients with severe haemophilia A due to intron 22 inversion with and without inhibitors of factor VIII
    • Oldenburg J, Picard JK, Schwaab R, Brackmann HH, Tuddenham EG, Simpson E. HLA genotype of patients with severe haemophilia A due to intron 22 inversion with and without inhibitors of factor VIII. Thromb Haemost 1997; 77: 238-42.
    • (1997) Thromb Haemost , vol.77 , pp. 238-242
    • Oldenburg, J.1    Picard, J.K.2    Schwaab, R.3    Brackmann, H.H.4    Tuddenham, E.G.5    Simpson, E.6
  • 13
    • 0842333021 scopus 로고    scopus 로고
    • Intensive exposure to factor VIII is a risk factor for inhibitor development in mild hemophilia A
    • Sharathkumar A, Lillicrap D, Blanchette VS et al. Intensive exposure to factor VIII is a risk factor for inhibitor development in mild hemophilia A. J Thromb Haemost 2003; 1: 1228-36.
    • (2003) J Thromb Haemost , vol.1 , pp. 1228-1236
    • Sharathkumar, A.1    Lillicrap, D.2    Blanchette, V.S.3
  • 14
    • 84860767903 scopus 로고    scopus 로고
    • How we choose factor VIII to treat hemophilia
    • Mannucci PM, Mancuso ME, Santagostino E. How we choose factor VIII to treat hemophilia. Blood 2012; 119: 4108-14.
    • (2012) Blood , vol.119 , pp. 4108-4114
    • Mannucci, P.M.1    Mancuso, M.E.2    Santagostino, E.3
  • 15
    • 79952066899 scopus 로고    scopus 로고
    • Harmonization of clinical trial guidelines for assessing the risk of inhibitor development in hemophilia A treatment
    • Aledort LM. Harmonization of clinical trial guidelines for assessing the risk of inhibitor development in hemophilia A treatment. J Thromb Haemost 2011; 9: 423-7.
    • (2011) J Thromb Haemost , vol.9 , pp. 423-427
    • Aledort, L.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.