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Emicizumab in the treatment of acquired hemophilia A: A Two-Center experience [PDF]

open access: yesAnnals of Hematology
Emicizumab is a FVIII mimetic antibody used in the treatment of inherited hemophilia A that could potentially be used in acquired hemophilia A (AHA) to achieve hemostasis and shorten hospital stay while reducing bypass therapies. We report on 12 cases of
Malcolm Su   +3 more
doaj   +2 more sources

Augmented emicizumab-driven coagulation potential in hemophilia A state by in vitro and in vivo supplementation of combined factors IX and X [PDF]

open access: yesResearch and Practice in Thrombosis and Haemostasis
Background: Persons with hemophilia A (HA) and inhibitors undergoing emicizumab prophylaxis require bypassing agents when breakthrough bleeding occurs.
Mitsumasa Osuna   +4 more
doaj   +2 more sources

Anti-emicizumab antibodies and their relevance in clinical practice [PDF]

open access: yesResearch and Practice in Thrombosis and Haemostasis
Background: Emicizumab is licensed for treatment of people with hemophilia A (HA) of all ages, with and without factor (F)VIII inhibitors. It is well tolerated, and most of the treatment-related adverse events are of mild intensity and transient.
Carla Valsecchi   +5 more
doaj   +2 more sources

Emicizumab in children: bleeding episodes and outcome before and after transition to Emicizumab

open access: yesBMC Pediatrics, 2022
Purpose Real-world data and study data regarding therapy with Emicizumab in pediatric cohorts with haemophilia A is scarce. Especially, data on previously untreated pediatric patients (PUPs) and minimally treated patients (MTPs) are missing.
Hannah Glonnegger   +5 more
doaj   +4 more sources

Clinical Experience with Emicizumab and Rituximab as First-Line Treatment in a Case Series of Acquired Hemophilia A [PDF]

open access: yesHematology Reports
Background: Acquired hemophilia A (AHA) is a bleeding disorder caused by autoantibodies against coagulation factor VIII. Treatment includes controlling bleeding and eliminating the inhibitor.
Hikari Ota   +3 more
doaj   +2 more sources

Quantification of emicizumab by mass spectrometry in plasma of people with hemophilia A: A method validation study

open access: yesResearch and Practice in Thrombosis and Haemostasis, 2022
Background Emicizumab is a new treatment option for people with hemophilia A. Emicizumab was approved with a body‐weight‐based dosage regimen, without laboratory monitoring requirements.
Moniek De Maat   +2 more
exaly   +2 more sources

Emicizumab state‐of‐the‐art update

open access: yesHaemophilia, 2022
AbstractIntroductionEmicizumab is a bispecific monoclonal antibody developed to address the unmet needs of clotting factor replacement therapy and has become the benchmark for optimal prophylaxis in managing patients with haemophilia A with inhibitors.
Johnny Mahlangu   +2 more
exaly   +4 more sources

Emicizumab prophylaxis in a preterm infant with severe hemophilia A: a case report on the feasibility of early use [PDF]

open access: yesResearch and Practice in Thrombosis and Haemostasis
Background: Emicizumab provides effective prophylaxis for hemophilia A (HA), but evidence for preterm and very low-birth-weight infants remains limited. Key Clinical Question: Can emicizumab be safely initiated shortly after birth in a preterm, low-birth-
Eman Hassan   +6 more
doaj   +2 more sources

Importance of Inhibitor Surveillance During Emicizumab Prophylaxis in Young Children With Hemophilia: An Illustrative Case Series [PDF]

open access: yesCase Reports in Hematology
Hemophilia is an X-linked inherited bleeding disorder associated with bleeding, which starts in infancy. The age of initiation of prophylaxis with clotting factor concentrate is limited by the intravenous mode of administration. Emicizumab, a Factor VIII
Kelly A. Bush   +3 more
doaj   +2 more sources

NXT007 enhances in vitro coagulation potential in the coexistence of emicizumab in hemophilia A through distinct complex formation [PDF]

open access: yesResearch and Practice in Thrombosis and Haemostasis
Background: NXT007 is a factor (F)VIIIa-mimetic bispecific antibody (BsAb) for hemophilia A (HA), engineered from emicizumab. It is designed to achieve non-hemophiliac levels of plasma coagulation potential and is currently under clinical development. In
Kazuki Yamaguchi   +7 more
doaj   +2 more sources

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