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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

AstraZeneca (AZN) announces Ultomiris approved in the US for NMOSD

AstraZeneca (AZN) announces Ultomiris approved in the US for NMOSD
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United statesSeanj pittockMarc dunoyerMayo neuroimmunology laboratoryMayo clinic centerEuropean unionDrug administrationMayo clinicMultiple sclerosisAutoimmune neurologyNeuroimmunology laboratoryChief executive officer

AstraZeneca : Ultomiris approved in the US for the treatment of adults with neuromyelitis optica spectrum disorder (NMOSD) - Form 6-K -March 25, 2024 at 07:31 am EDT

a0626i FORM 6-K SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 Report of Foreign Issuer Pursuant to Rule 13a-16 or.

United statesUnited kingdomNew zealandMarc dunoyerSeanj pittockAdrian kempNeuromyelitis opticaHistochem cytochemDrug administrationMayo neuroimmunology laboratoryMayo clinic centerSecurities exchangeEuropean unionInvestor relations teamAlexion pharmaceuticals incCommission file number

Ultomiris Receives FDA Approval as First Long-Acting Treatment for AQP4 Ab+ NMOSD, Redefining Patient Care

Ultomiris Receives FDA Approval as First Long-Acting Treatment for AQP4 Ab+ NMOSD, Redefining Patient Care
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United kingdomNew zealandUnited statesNeuromyelitis opticaMarc dunoyerAdrian kempHistochem cytochemSeanj pittockAlexion pharmaceuticals incMayo clinic centerEuropean unionDrug administrationMayo neuroimmunology laboratoryUltomiris receivesFirst long acting treatmentRedefining patient

FDA Approves Ravulizumab-cwvz for Neuromyelitis Optica Spectrum Disorder

Zero relapses were reported among individuals that received ravulizumab-cwvz over the 73 weeks of treatment.

United statesSeanj pittockAlexion pharmaceuticals incMayo clinic centerMayo neuroimmunology laboratoryAlexion pharmaceuticalsMayo clinicMultiple sclerosisAutoimmune neurologyNeuroimmunology laboratorySafety studyAdult participants withNorth americaExpanded disability status scale score