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AstraZeneca demonstrates commitment to patients living with amyloidosis at the 2024 International Symposium on Amyloidosis (ISA)

AstraZeneca demonstrates commitment to patients living with amyloidosis at the 2024 International Symposium on Amyloidosis (ISA)
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United statesUnited kingdomChristophe hotermansSarah waltersWaddington cruzWorld analysis utilizing electronic health recordsElectronic health records database analysisInternational symposium on amyloidosisElectronic health recordsIonis pharmaceuticalsHead of global medical affairsDrug administrationAstrazeneca pharmaceuticalsColumbia university irving medical centerAstrazeneca rare diseaseInternational symposium

Eplontersen granted U S FDA Fast Track designation for patients with transthyretin-mediated amyloid cardiomyopathy

CARLSBAD, Calif., Feb. 8, 2024 /PRNewswire/ Ionis Pharmaceuticals, Inc. announced today that the U.S. Food and Drug Administration has granted Fast Track designation to Ionis and AstraZeneca s.

Sarah waltersEugene schneiderIonis pharmaceuticalsDrug administrationIonis pharmaceuticals incColumbia university irving medical centerFast trackOrphan drug designationTransthyretin mediated amyloid cardiomyopathyConjugated antisenseSerum vitaminRecommended supplementationPrescribing informationUniversity irving medical centerDrug reduces deathUnderdiagnosed form

WAINUA™ (eplontersen) Granted First-Ever Regulatory Approval in the US for the Treatment of Adults With Polyneuropathy of Hereditary Transthyretin-Mediated Amyloidosis

WAINUA™ (eplontersen) Granted First-Ever Regulatory Approval in the US for the Treatment of Adults With Polyneuropathy of Hereditary Transthyretin-Mediated Amyloidosis
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United statesUnited kingdomIsabelle lousadaBrendan mcevoyMichaelj polydefkisChelsea tresslerEuropean parliamentCommission implementing decisionColumbia university irving medical centerIonis pharmaceuticalsDrug administrationAmyloidosis research consortiumEuropean commissionJournal of the american medical associationNeuropathy impairment scoreNorfolk quality

WAINUAtm (eplontersen) Granted First-Ever Regulatory Approval in the US for the Treatment of Adults With Polyneuropathy of Hereditary Transthyretin-Mediated Amyloidosis

WAINUAtm (eplontersen) Granted First-Ever Regulatory Approval in the US for the Treatment of Adults With Polyneuropathy of Hereditary Transthyretin-Mediated Amyloidosis
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United kingdomUnited statesMichaelj polydefkisIsabelle lousadaColumbia university irving medical centerProduct serviceAmyloidosis research consortiumCommission implementing decisionJournal of the american medical associationIonis pharmaceuticalsEuropean commissionEuropean parliamentDrug administrationGranted first ever regulatory approvalAdults with polyneuropathyHereditary transthyretin mediated

AstraZeneca s Wainua receives FDA approval in the US

AstraZeneca's Wainua receives FDA approval in the US

United statesIsabelle lousadaMichaelj polydefkisColumbia university irving medical centerEuropean parliamentDrug administrationJournal of the american medical associationCommission implementing decisionAmyloidosis research consortiumIonis pharmaceuticalsEuropean commissionNeuropathy impairment scoreNorfolk qualityLife questionnaire diabetic neuropathyAmerican medical associationJohns hopkins university school