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Participant is aged 2 to less than (\\\u003C) 12 years at the time of lanadelumab initiation and is expected to have at least 6 months of follow-up information before turning 12.\n2. Participant has physician-confirmed diagnosis of HAE-C1INH.\n3. Participant initiated LTP with lanadelumab during the eligibility period.\n4. Signed consent\u002Fassent (where required by local regulations).\n5. Participant's medical record contains documentation of HAE attacks in the pre-index period and after lanadelumab initiation.\n\nExclusion Criteria:\n\n1. Participant was enrolled in a therapeutic investigational drug (lanadelumab or other drug) or device trial at index date.\n2. Participant with no documented HAE attacks in the 12 months prior to index date.","ALL","2 Years","11 Years",{"count":392,"type":393},40,"ESTIMATED","OBSERVATIONAL","HAE is a rare condition. It causes sudden swelling under the skin and inside the body, like in the belly, throat, or genitals. 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This will be measured by checking how long children who receive lanadelumab will be free of HAE attacks.\n\nOther goals are to understand how children with HAE-C1INH deficiency are being treated with lanadelumab, how well the treatment works for them, how safe it is and how often these children need to use healthcare services (like doctor visits, hospital stays, etc.) because of their condition.\n\nThe study will only look at data already existing in the participants' medical records. No treatment will be given as part of the study.",[397],"Hereditary Angioedema (HAE)",[399],"Drug Therapy","2026-06-16",{"date":402,"type":403},"2026-06-18","ACTUAL",{"date":405,"type":403},"2026-02-05",{"date":407,"type":393},"2026-06-30",{"name":5,"class":6},24]