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Workplace Options: Psychological Safety in Today s Global Workforce

Workplace Options: Psychological Safety in Today s Global Workforce
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United statesUnited kingdomJennifer dartAlan kingBob batchelorMary ellen gornickDennis riedlTeam performanceCorporate communicationsWorkplace optionsDebuts data driven study acrossExplores workplace issuesInclusive leadershipRenewed commitmentSafety studyGlobal context

FDA Approves Vadadustat for Oral Treatment of Anemia Due to Chronic Kidney Disease

Vadadustat (Vafseo; Akebia Therapeutics Inc) is indicated for individuals with chronic kidney disease who have been receiving dialysis for at least 3 months.

Safety studyEvaluate vadadustatMaintenance treatment

AstraZeneca Ultomiris granted approval in US for treatment of adults with neuromyelitis optica spectrum disorder

Ultomiris, the first long-acting C5 complement inhibitor, shows promise in reducing relapse risk for AQP4 Ab+ NMOSD patients. Learn more here.

United kingdomNew zealandUnited statesNeuromyelitis opticaHistochem cytochemEuropean unionDrug administrationAlexion pharmaceuticals incNorth americaExpanded disability status scale scoreAstrazeneca rare diseaseAlexion pharmaceuticalsRare diseasesAnn neurolCurr treat optionsSouth east

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

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