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ACE910

 
National Institutes of Health

Papers overview

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Review
2019
Review
2019
Congenital hemophilia A, a relatively common and sometimes life-threatening bleeding disorder, is caused by inherited deficiency… Expand
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Highly Cited
2016
Highly Cited
2016
ACE910 is a recombinant humanized bispecific antibody that binds to activated factor IX and factor X and mimics the cofactor… Expand
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2016
2016
The development of inhibitors to factor VIII (FVIII) or factor IX (FIX) remains a major treatment complication encountered in the… Expand
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Review
2016
Review
2016
  • K. Nogami
  • Thrombosis research
  • 2016
  • Corpus ID: 13037506
There are some issues in the current factor (F)VIII replacement therapy for severe hemophilia A. One is mental and physical… Expand
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2015
2015
Background: ACE910, a humanized bispecific antibody to factor (F) IXa and FX mimicking the functions of FVIII, exerts tenase… Expand
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2015
2015
  • M. Shima
  • [Rinsho ketsueki] The Japanese journal of…
  • 2015
  • Corpus ID: 43470396
Unmet needs of current hemophilia A treatment include the requirement for frequent intravenous infusions, inhibitor development… Expand
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Highly Cited
2014
Highly Cited
2014
ACE910 is a humanized anti-factor IXa/X bispecific antibody mimicking the function of factor VIII (FVIII). We previously… Expand
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  • table 1
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Highly Cited
2014
Highly Cited
2014
We previously reported that a humanized anti‐factor IXa/X bispecific antibody, hBS23, mimics the function of FVIII even in the… Expand
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2014
2014
BACKGROUND We previously reported that a humanized anti-factor IXa/X bispecific antibody, hBS23, mimics the function of FVIII… Expand
Is this relevant?
2014
2014
Background: Although routine supplementation of exogenous factor VIII (FVIII) effectively prevents bleeding complications in… Expand
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