Latest Breaking News On - Jorge Capapey

Alnylam s RNAi therapeutic expanded by FDA in advanced primary hyperoxaluria type 1

Alnylam s RNAi therapeutic expanded by FDA in advanced primary hyperoxaluria type 1
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Jorge capapeyAlnylam pharmaceuticalsEuropean medicines agencyDrug administrationAlnylam pharmaceutical

Alnylam Announces FDA Approval of Supplemental New Drug Application for OXLUMO® (lumasiran) in Advanced Primary Hyperoxaluria Type 1

Alnylam Announces FDA Approval of Supplemental New Drug Application for OXLUMO® (lumasiran) in Advanced Primary Hyperoxaluria Type 1
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United kingdomUnited statesChristine regan lindenboomJorge capapeyJosh brodskyKim hollanderHyperoxaluria foundationGlobal rare disease lead at alnylam pharmaceuticalsDrug administrationAlnylam pharmaceuticals incExchange commissionAlnylam pharmaceuticalsEuropean medicines agencyCommittee for medicinal products human usePrimary hyperoxaluria typeLower urinary

Alnylam Announces FDA Approval of Supplemental New Drug Application for OXLUMO® (lumasiran) in Advanced Primary Hyperoxaluria Type 1 - Alnylam Pharmaceuticals (NASDAQ:ALNY) - Press Release

- OXLUMO Now Indicated for the Treatment of Primary Hyperoxaluria Type 1 (PH1) to Lower Urinary and Plasma Oxalate Levels in Pediatric and Adult Patie

United statesUnited kingdomJorge capapeyKim hollanderHyperoxaluria foundationGlobal rare disease lead at alnylam pharmaceuticalsDrug administrationAlnylam pharmaceuticals incExchange commissionAlnylam pharmaceuticalsEuropean medicines agencyCommittee for medicinal products human usePrimary hyperoxaluria typeLower urinaryPlasma oxalate levelsAdult patients

Alnylam Pharma (ALNY) Announces FDA Approval of Supplemental New Drug Application for OXLUMO

Alnylam Pharma (ALNY) Announces FDA Approval of Supplemental New Drug Application for OXLUMO
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United kingdomUnited statesChristine regan lindenboomJorge capapeyJosh brodskyKim hollanderHyperoxaluria foundationGlobal rare disease lead at alnylam pharmaceuticalsDrug administrationAlnylam pharmaceuticals incExchange commissionAlnylam pharmaceuticalsEuropean medicines agencyCommittee for medicinal products human useNew drug applicationVice president

FDA approves label expansion of Alnylam s Oxlumo for PH1

The US FDA has approved Alnylam Pharmaceuticals’ sNDA for the expanded use of Oxlumo (lumasiran) to treat advanced primary hyperoxaluria type 1 (PH1).

Jorge capapeyAlnylam pharmaceuticals global rare diseasePharmaceuticals global rare disease

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