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Epilepsy Awareness Day: 70 pc of patients can live normal life with medicines, says expert

Epilepsy Awareness Day: 70 pc of patients can live normal life with medicines, says expert
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New delhiManjari tripathiInternational epilepsy dayHead of the neurology departmentEpilepsy awareness dayEpilepsy dayNeurology department

Former general manager Terry Ryan, longtime coach Rick Stelmaszek elected to Twins Hall of Fame

The duo will be inducted into the Twins Hall of Fame on Aug. 10.

United statesUniversity of minnesotaRoyce lewisSamantha hobertDenny hockingCarlos correaDenny neagleMike radcliffChuck knoblauchJoe nathanByron buxtonRick stelmaszekFrancisco lirianoBoof bonserScott ericksonJoe mauer

Alnylam s AMVUTTRA Gets Approval In Europe To Treat Hereditary Transthyretin-mediated Amyloidosis

BRUSSELS/FRANKFURT/PARIS (dpa-AFX) - RNAi therapeutics company Alnylam Pharmaceuticals, Inc. (ALNY) announced Tuesday that the European Commission has granted marketing authorization for AMVUTTRA

France generalBruxelles capitaleDavid adamsHead of the neurology departmentEuropean commissionDrug administrationAlnylam pharmaceuticals incBrazilian health regulatory agencyJapanese pharmaceuticalsEuropean unionUniversity of parisDevices agencyAlnylam pharmaceuticalsLead investigatorOrphan drug designationMedical devices

Alnylam Receives Approval in Europe for AMVUTTRA® (vutrisiran) for the Treatment of Hereditary Transthyretin-mediated (hATTR) Amyloidosis in Adult Patients with Stage 1 or Stage 2 Polyneuropathy

– AMVUTTRA Demonstrated Halting or Reversal in Neuropathy Impairment with Subcutaneous Administration Once Every Three Months – – Decision Follows Positive Opinion from the. | September 20, 2022

United kingdomFrance generalKasha witkosDavid adamsHead of the neurology departmentEuropean commissionDrug administrationAlnylam pharmaceuticals incAlnylam pharmaceuticalsExchange commissionBrazilian health regulatory agencyHead international region at alnylamJapanese pharmaceuticalsEuropean unionUniversity of parisDevices agency

Alnylam Receives Approval in Europe for AMVUTTRA (vutrisiran) for the Treatment of Hereditary Transthyretin-mediated (hATTR) Amyloidosis in Adult Patients with Stage 1 or Stage 2 Polyneuropathy

The EC approval is based on positive 18-month results from the HELIOS-A Phase 3 study, where AMVUTTRA significantly improved the signs and symptoms of hATTR amyloidosis, with more than 50 percent of patients experiencing halting or reversal of their polyneuropathy manifestations.

France generalUnited kingdomKasha witkosDavid adamsSubcutaneous administration once every three monthsHead of the neurology departmentEuropean commissionDrug administrationAlnylam pharmaceuticals incAlnylam pharmaceuticalsBrazilian health regulatory agencyHead international region at alnylamJapanese pharmaceuticalsEuropean unionEuropean medicines agencyUniversity of paris

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