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    [{"orgOrder":0,"company":"CSL Behring","sponsor":"Not Applicable","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"U.S. Food and Drug Administration Approves HAEGARDA\u00ae for Prevention of Hereditary Angioedema (HAE) Attacks in Pediatric Patients","therapeuticArea":"Genetic Disease","highestDevelopmentStatus":"Approved","country":"U.S.A","productType":"Large molecule","productStatus":"Approved","date":"September 2020","url1":"","url2":"","graph1":"Genetic Disease","graph2":"Approved"}]

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    Human C1 Esterase Inhibitor

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              U.S. Food and Drug Administration Approves HAEGARDA® for Prevention of Hereditary Angioedema (HAE) Attacks in Pediatric Patients

              Details:

              The latest FDA approval was based on results from two CSL Behring-sponsored COMPACT trials. In the COMPACT pivotal study, HAEGARDA, at the FDA approved dose of 60 IU/kg, reduced the number of HAE attacks by a median of 95% relative to placebo.

              Lead Product(s): Human C1 Esterase Inhibitor

              Therapeutic Area: Genetic Disease Product Name: Haegarda

              Highest Development Status: Approved Product Type: Large molecule

              Partner/Sponsor/Collaborator: Not Applicable

              Deal Size: Not Applicable Upfront Cash: Not Applicable

              Deal Type: Not Applicable September 28, 2020

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