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Hemophilia A Pipeline Drugs Analysis Report, 2024 Updates: FDA

Hemophilia A Pipeline Drugs Analysis Report, 2024 Updates: FDA
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VOYDEYA™ approved in the US as add-on therapy to ravulizumab or eculizumab for treatment of extravascular hemolysis in adults with the rare disease PNH

VOYDEYA™ approved in the US as add-on therapy to ravulizumab or eculizumab for treatment of extravascular hemolysis in adults with the rare disease PNH
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AstraZeneca Ultomiris gets USFDA approval for adults with neuromyelitis optica spectrum disorder

Ultomiris, a long-acting C5 complement inhibitor, provides immediate, complete and sustained complement inhibition.

United statesMarc dunoyerSeanj pittockMayo clinic centerMayo neuroimmunology laboratoryEuropean unionDrug administrationMayo clinicMultiple sclerosisAutoimmune neurologyNeuroimmunology laboratoryChief executive officerNorth americaExpanded disability status scale scoreAstrazenec newsRavulizumab cwvz

ULTOMIRIS® (ravulizumab-cwvz) approved in the US for the treatment of adults with neuromyelitis optica spectrum disorder (NMOSD)

First and only long-acting C5 complement inhibitor offers patients with AQP4 Ab+ NMOSD the potential to live relapse-free Unprecedented relapse risk reduction observed in CHAMPION-NMOSD trial.

United kingdomNew zealandUnited statesNeuromyelitis opticaHistochem cytochemAlexion pharmaceuticals incDrug administrationParoxysmal nocturnal hemoglobinuriaHemolytic uremic syndromeMyasthenia gravisNeuromyelitis optica spectrum disorderPatient safety cardMitigation strategyPrescribing informationMedication guideNorth america

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