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Health Canada Grants Marketing Authorization for TRIKAFTA® (elexacaftor/tezacaftor/ivacaftor and ivacaftor) in Children With Cystic Fibrosis Ages 6 Through 11 years With At Least One F508del Mutation

-Approximately 500 Canadians ages 6-11 are now eligible for TRIKAFTA®- -Vertex has submitted this indication to CADTH & INESSS for Health Technology Assessments- . | April 20, 2022

United statesUnited kingdomCity ofReshma kewalramaniMcgill university health centerExchange commissionCanadian agency for drugsPediatric pulmonary function laboratoryHealth technology assessmentsHealth canadaTechnologies in healthMcgill universityDepartment of pediatricsVertex pharmaceuticals incorporated nasdaqVertex pharmaceuticals incorporatedMarketing authorization

BRIEF—Health Canada approval for Trikafta in six to 11 year-olds

BRIEF—Health Canada approval for Trikafta in six to 11 year-olds
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Health Canada approves Vertex s Trikafta for cystic fibrosis in children

Health Canada issued marketing authorisation to Vertex Pharmaceuticals' Trikafta for children with cystic fibrosis aged six to 11 years.

Reshma kewalramaniVertex pharmaceuticalsCanadian agency for drugsHealth technology assessmentsEuropean commissionHealth canadaTechnologies in healthVertex pharmaceuticals incorporatedCanadian agencyHealth technologyVertex pharmaceutical kaftrioMeasurement instrumentsChain refrigeratedProcess technologies

Vital Signs: Digital Health Law Update Winter 2022 | Jones Day

Note From the Editors With 2022 well underway, the rapid pace of statutory, regulatory, policy, and industry activities in digital health continues in force. We bring you Vital Signs, a.

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Aytu BioPharma Announces AR101 Granted Orphan Designation in Europe for the Treatment of Ehlers-Danlos Syndrome

Aytu BioPharma Announces AR101 Granted Orphan Designation in Europe for the Treatment of Ehlers-Danlos Syndrome
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Aytu biopharmaChelcie listerJosh disbrowEuropean commissionDrug administrationExchange commissionStrategic communicationsAytu biopharma incSecurities exchangeEuropean medicines agencyHealth technology assessmentsEhlers danlos syndromeOrphan medicinal productsFull prescribing informationOrphan drugEuropean medicines