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Volumn 11, Issue 4, 2010, Pages 472-478

Velaglucerase alfa, a human recombinant glucocerebrosidase enzyme replacement therapy for type 1 Gaucher disease

Author keywords

[No Author keywords available]

Indexed keywords

IMIGLUCERASE; RECOMBINANT ENZYME; UNCLASSIFIED DRUG; VELAGLUCERASE ALFA;

EID: 77950118269     PISSN: 14724472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (14)

References (31)
  • 1
    • 77950126850 scopus 로고    scopus 로고
    • Phase I/II, nine month study results of enzyme replacement therapy with gene activated human glucocerebrosidase (GA-GCB) in patients with type i Gaucher disease
    • Phase I/II, nine month study results of enzyme replacement therapy with gene activated human glucocerebrosidase (GA-GCB) in patients with type I Gaucher disease. Zimran A, Fratazzi C, Mensah R, Elstein D BLOOD 2005 106 11 Abs 3882
    • (2005) BLOOD , vol.106 , Issue.11 , pp. 3882
    • Zimran, A.1    Fratazzi, C.2    Mensah, R.3    Elstein, D.4
  • 2
    • 33745722913 scopus 로고    scopus 로고
    • Superior effects of high-dose enzyme replacement therapy in type 1 Gaucher disease on bone marrow involvement and chitotriosidase levels: A 2-center retrospective analysis
    • Superior effects of high-dose enzyme replacement therapy in type 1 Gaucher disease on bone marrow involvement and chitotriosidase levels: A 2-center retrospective analysis. de Fost M, Hollak CEM, Greener JEM, Aerts JMFG, Maas M, Poll LW, Wiersma MG, Haussinger D, Brett S, Brill N, vom Dahl S BLOOD 2006 108 3 830-835
    • (2006) BLOOD , vol.108 , Issue.3 , pp. 830-835
    • De Fost, M.1    Hollak, C.E.M.2    Greener, J.E.M.3    Aerts, J.M.F.G.4    Maas, M.5    Poll, L.W.6    Wiersma, M.G.7    Haussinger, D.8    Brett, S.9    Brill, N.10    Vom Dahl, S.11
  • 3
    • 77950158516 scopus 로고    scopus 로고
    • Phase I/II, 9-month study results of enzyme replacement therapy with gene-activated human glucocerebrosidase in patients with type 1 Gaucher disease
    • Phase I/II, 9-month study results of enzyme replacement therapy with gene-activated human glucocerebrosidase in patients with type 1 Gaucher disease. Zimran A, Fratazzi C, Altarescu G, Mensah R, Elstein D ACTA PAEDIATR 2007 96 Suppl 455 106
    • (2007) ACTA PAEDIATR , vol.96 , Issue.SUPPL. 455 , pp. 106
    • Zimran, A.1    Fratazzi, C.2    Altarescu, G.3    Mensah, R.4    Elstein, D.5
  • 4
    • 77950145797 scopus 로고    scopus 로고
    • Phase I/II study of glucocerebrosidase replacement therapy in patients with type i Gaucher disease
    • Phase I/II study of glucocerebrosidase replacement therapy in patients with type I Gaucher disease. Zimran A, Elstein D, Loveday K, Aliski W, Fratazzi C ACTA PAEDIATR 2006 95 Suppl 451 143
    • (2006) ACTA PAEDIATR , vol.95 , Issue.SUPPL. 451 , pp. 143
    • Zimran, A.1    Elstein, D.2    Loveday, K.3    Aliski, W.4    Fratazzi, C.5
  • 5
    • 77950130237 scopus 로고    scopus 로고
    • Months on treatment: Open-label phase I/II long-term study of enzyme replacement therapy (ERT) with "gene-activated" human glucocerebrosidase (GA-GCB) in patients with type i Gaucher disease
    • months on treatment: Open-label phase I/II long-term study of enzyme replacement therapy (ERT) with "gene-activated" human glucocerebrosidase (GA-GCB) in patients with type I Gaucher disease. Zimran A, Bhirangi K, Mensah R, Altarescu G, Elstein D MOL GENET METAB 2008 93 2 Abs 118
    • (2008) MOL GENET METAB , vol.93 , Issue.2 , pp. 118
    • Zimran, A.1    Bhirangi, K.2    Mensah, R.3    Altarescu, G.4    Elstein, D.5
  • 6
    • 77950183415 scopus 로고    scopus 로고
    • A study of Genz-112638 in patients with Gaucher disease
    • NCT00891202: A study of Genz-112638 in patients with Gaucher disease. Genzyme CLINICALTRIALS.GOV 2009
    • (2009) Genzyme CLINICALTRIALS.GOV
  • 7
    • 34248504877 scopus 로고    scopus 로고
    • A pharmacokinetic analysis of a novel enzyme replacement therapy with gene-activated human glucocerebrosidase (GA-GCB) in patients with type 1 Gaucher disease
    • A pharmacokinetic analysis of a novel enzyme replacement therapy with gene-activated human glucocerebrosidase (GA-GCB) in patients with type 1 Gaucher disease. Zimran A, Loveday K, Fratazzi C, Elstein D BLOOD CELLS MOL DIS 2007 39 1 115-118
    • (2007) BLOOD CELLS MOL DIS , vol.39 , Issue.1 , pp. 115-118
    • Zimran, A.1    Loveday, K.2    Fratazzi, C.3    Elstein, D.4
  • 8
    • 77950105973 scopus 로고    scopus 로고
    • Months on treatment: Open-label phase I/II long-term study of enzyme replacement therapy (ERT) with gene-activated human glucocerebrosidase (GA-GCB) in patients with type i Gaucher disease
    • 24-months on treatment: Open-label phase I/II long-term study of enzyme replacement therapy (ERT) with gene-activated human glucocerebrosidase (GA-GCB) in patients with type I Gaucher disease. Zimran A, Altarescu G, Fratazzi C, Mensah R, Elstein D MOL GENET METAB 2007 92 4 Abs 22
    • (2007) MOL GENET METAB , vol.92 , Issue.4 , pp. 22
    • Zimran, A.1    Altarescu, G.2    Fratazzi, C.3    Mensah, R.4    Elstein, D.5
  • 9
    • 77950112420 scopus 로고    scopus 로고
    • Supply shortages of Cerezyme and Fabrazyme - Priority access for patients most in need of treatment recommended
    • June 25
    • Supply shortages of Cerezyme and Fabrazyme - Priority access for patients most in need of treatment recommended. European Agency for the Evaluation of Medicinal Products PRESS RELEASE 2009 June 25
    • (2009) European Agency for the Evaluation of Medicinal Products PRESS RELEASE
  • 10
    • 77950112419 scopus 로고    scopus 로고
    • Shire completes submission of NDA for velaglucerase alfa for type 1 Gaucher disease and reports positive results for remaining two phase III trials
    • September 01
    • Shire completes submission of NDA for velaglucerase alfa for type 1 Gaucher disease and reports positive results for remaining two phase III trials. Shire plc PRESS RELEASE 2009 September 01
    • (2009) Shire Plc PRESS RELEASE
  • 11
    • 77950136843 scopus 로고    scopus 로고
    • Shire plc Q3 2009 earnings call
    • November 01
    • Shire plc Q3 2009 earnings call. Shire plc COMPANY PRESENTATION 2009 November 01
    • (2009) Shire Plc COMPANY PRESENTATION
  • 12
    • 77950101447 scopus 로고    scopus 로고
    • Shire submits European Marketing Authorization Application (MAA) for velaglucerase alfa for the treatment of Type 1 Gaucher disease
    • November 24
    • Shire submits European Marketing Authorization Application (MAA) for velaglucerase alfa for the treatment of Type 1 Gaucher disease. Shire plc PRESS RELEASE 2009 November 24
    • (2009) Shire Plc PRESS RELEASE
  • 13
    • 77950106899 scopus 로고    scopus 로고
    • Pfizer and Protalix enter into agreement to develop and commercialize Gaucher's disease treatment
    • December 01
    • Pfizer and Protalix enter into agreement to develop and commercialize Gaucher's disease treatment. Pfizer Inc PRESS RELEASE 2009 December 01
    • (2009) Pfizer Inc PRESS RELEASE
  • 14
    • 77950148865 scopus 로고    scopus 로고
    • Genzyme begins shipping newly produced Cerezyme from Allston plant
    • December 01
    • Genzyme begins shipping newly produced Cerezyme from Allston plant. Genzyme Corp Press Release 2009 December 01
    • (2009) Genzyme Corp Press Release
  • 16
    • 53449086596 scopus 로고    scopus 로고
    • Gaucher disease: New developments in treatment and etiology
    • Gaucher disease: New developments in treatment and etiology. Harmanci O, Bayraktar Y WORLD J GASTROENTEROL 2008 14 25 3968-3973
    • (2008) WORLD J GASTROENTEROL , vol.14 , Issue.25 , pp. 3968-3973
    • Harmanci, O.1    Bayraktar, Y.2
  • 22
    • 75149112725 scopus 로고    scopus 로고
    • Recombinant glucocerebrosidase (imiglucerase) as a therapy for Gaucher disease
    • Recombinant glucocerebrosidase (imiglucerase) as a therapy for Gaucher disease. Pastores GM BIODRUGS 2010 24 1 41-47
    • (2010) BIODRUGS , vol.24 , Issue.1 , pp. 41-47
    • Pastores, G.M.1
  • 23
    • 84976877289 scopus 로고    scopus 로고
    • Five-year safety and efficacy of velaglucerase alfa in Gaucher disease type 1: Experience in clinic and home settings
    • February 12
    • Five-year safety and efficacy of velaglucerase alfa in Gaucher disease type 1: Experience in clinic and home settings. Elstein D, Zimran A, Cohn GM, Bhirangi K LYSOSOMAL DIS NETWORK: WORLD ANN SYMP 2010 6 February 12 Abs 49
    • (2010) LYSOSOMAL DIS NETWORK: WORLD ANN SYMP , vol.6 , pp. 49
    • Elstein, D.1    Zimran, A.2    Cohn, G.M.3    Bhirangi, K.4
  • 24
    • 77950107328 scopus 로고    scopus 로고
    • Enzyme replacement therapy with velaglucerase alfa significantly improves key clinical parameters in type 1 Gaucher disease: Positive results from a randomized, double-blind, global, phase III study
    • February 12
    • Enzyme replacement therapy with velaglucerase alfa significantly improves key clinical parameters in type 1 Gaucher disease: Positive results from a randomized, double-blind, global, phase III study. Zimran A, Gonzalez D, Lukina EA, Ben Dridi M-F, Kisinovsky I, Crombez E, Bhirangi K LYSOSOMAL DIS NETWORK: WORLD ANN SYMP 2010 6 February 12 Abs 157
    • (2010) LYSOSOMAL DIS NETWORK: WORLD ANN SYMP , vol.6 , pp. 157
    • Zimran, A.1    Gonzalez, D.2    Lukina, E.A.3    Ben Dridi, M.-F.4    Kisinovsky, I.5    Crombez, E.6    Bhirangi, K.7
  • 25
    • 77950122387 scopus 로고    scopus 로고
    • Enzyme replacement therapy with velaglucerase alfa improves key clinical parameters in a pediatric subgroup with type 1 Gaucher disease
    • February 12
    • Enzyme replacement therapy with velaglucerase alfa improves key clinical parameters in a pediatric subgroup with type 1 Gaucher disease. Zimran A, Gonzalez D, Crombez E, Bhirangi K LYSOSOMAL DIS NETWORK: WORLD ANN SYMP 2010 6 February 12 Abs 156
    • (2010) LYSOSOMAL DIS NETWORK: WORLD ANN SYMP , vol.6 , pp. 156
    • Zimran, A.1    Gonzalez, D.2    Crombez, E.3    Bhirangi, K.4
  • 28
    • 62149144047 scopus 로고    scopus 로고
    • Dosing enzyme replacement therapy for Gaucher disease: Older, but are we wiser?
    • Dosing enzyme replacement therapy for Gaucher disease: Older, but are we wiser? Sidransky E, Pastores GM, Mori M GENET MED 2009 11 2 90-91
    • (2009) GENET MED , vol.11 , Issue.2 , pp. 90-91
    • Sidransky, E.1    Pastores, G.M.2    Mori, M.3
  • 29
    • 77950172786 scopus 로고    scopus 로고
    • Shire presents positive efficacy and safety data for velaglucerase alfa in treatment of naïve patients with type 1 Gaucher disease
    • February 11
    • Shire presents positive efficacy and safety data for velaglucerase alfa in treatment of naïve patients with type 1 Gaucher disease. Shire plc PRESS RELEASE 2010 February 11
    • (2010) Shire Plc PRESS RELEASE
  • 30
    • 77950182075 scopus 로고    scopus 로고
    • Excellent results in a transformational year for Shire; Core product sales up 25%
    • February 19
    • Excellent results in a transformational year for Shire; Core product sales up 25%. Shire plc PRESS RELEASE 2010 February 19
    • (2010) Shire Plc PRESS RELEASE
  • 31
    • 77950166543 scopus 로고    scopus 로고
    • Shire announces FDA approval of VPRIV (velaglucerase alfa for injection) for the treatment of type 1 Gaucher disease
    • February 26
    • Shire announces FDA approval of VPRIV (velaglucerase alfa for injection) for the treatment of type 1 Gaucher disease. Shire plc Press Release 2010 February 26
    • (2010) Shire Plc Press Release


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.