<div><p>In hemophilia A, routine prophylaxis with exogenous factor VIII (FVIII) requires frequent intravenous injections and can lead to the development of anti-FVIII alloantibodies (FVIII inhibitors). To overcome these drawbacks, we screened asymmetric bispecific IgG antibodies to factor IXa (FIXa) and factor X (FX), mimicking the FVIII cofactor function. Since the therapeutic potential of the lead bispecific antibody was marginal, FVIII-mimetic activity was improved by modifying its binding properties to FIXa and FX, and the pharmacokinetics was improved by engineering the charge properties of the variable region. Difficulties in manufacturing the bispecific antibody were overcome by identifying a common light chain for the anti-FIXa and ...
Development of inhibitory antibodies to coagulation factor VIII (fVIII) is the primary obstacle to t...
Inhibitory antibodies directed against coagulation factor VIII (FVIII) can be found in patients with...
A significant proportion of haemophilia A patients receiving transfusions of Factor VIII (FVIII) dev...
In hemophilia A, routine prophylaxis with exogenous factor VIII (FVIII) requires frequent intravenou...
Development of neutralizing antibodies against biotherapeutic agents administered to prevent or trea...
Hemophilia A is a bleeding disorder, affecting about 400 000 people worldwide. In addition to prolon...
With the development of molecular cloning technology and the deep understanding of antibody engineer...
<p>(A) FVIII-mimetic activity of hBS910 in thrombin generation assay (TGA). Effect of hBS910 (circle...
<div><p>Inhibitory antibodies directed against coagulation factor VIII (FVIII) can be found in patie...
Development of inhibitory antibodies to coagulation factor VIII (fVIII) is the primary obstacle to t...
Bispecific antibodies combine two different antigen-binding sites in a single molecule, enabling mor...
<p>(A) Improving FVIII-mimetic activity of the bispecific antibody. Effect of hBS1 (circles), hBS106...
ABSTRACTFor patients with hemophilia A, replacement of deficient factor VIII (FVIII) using plasma-de...
Bispecific antibodies (bsAbs) are antibodies with two binding sites directed at different antigens, ...
Treatment of heamophilia A requires frequent infusion of plasma- or recombinant-derived factor VIII....
Development of inhibitory antibodies to coagulation factor VIII (fVIII) is the primary obstacle to t...
Inhibitory antibodies directed against coagulation factor VIII (FVIII) can be found in patients with...
A significant proportion of haemophilia A patients receiving transfusions of Factor VIII (FVIII) dev...
In hemophilia A, routine prophylaxis with exogenous factor VIII (FVIII) requires frequent intravenou...
Development of neutralizing antibodies against biotherapeutic agents administered to prevent or trea...
Hemophilia A is a bleeding disorder, affecting about 400 000 people worldwide. In addition to prolon...
With the development of molecular cloning technology and the deep understanding of antibody engineer...
<p>(A) FVIII-mimetic activity of hBS910 in thrombin generation assay (TGA). Effect of hBS910 (circle...
<div><p>Inhibitory antibodies directed against coagulation factor VIII (FVIII) can be found in patie...
Development of inhibitory antibodies to coagulation factor VIII (fVIII) is the primary obstacle to t...
Bispecific antibodies combine two different antigen-binding sites in a single molecule, enabling mor...
<p>(A) Improving FVIII-mimetic activity of the bispecific antibody. Effect of hBS1 (circles), hBS106...
ABSTRACTFor patients with hemophilia A, replacement of deficient factor VIII (FVIII) using plasma-de...
Bispecific antibodies (bsAbs) are antibodies with two binding sites directed at different antigens, ...
Treatment of heamophilia A requires frequent infusion of plasma- or recombinant-derived factor VIII....
Development of inhibitory antibodies to coagulation factor VIII (fVIII) is the primary obstacle to t...
Inhibitory antibodies directed against coagulation factor VIII (FVIII) can be found in patients with...
A significant proportion of haemophilia A patients receiving transfusions of Factor VIII (FVIII) dev...