Disease index

hereditary angioedema (HAE)

Rare disease · 2010–2024

4decisions
2medicines
2carried consumer input
2individual submissions

Every decision

MedicineMeetingOutcomeConsumer input
lanadelumab Preventative treatment of hereditary angioedema (HAE) Types 1 or 2 in patients aged 2 to 11 years who have experienced at least one treated acute attack within… Nov 2024 Recommended 2 individuals
icatibant Symptomatic treatment of acute attacks of hereditary angioedema (HAE) in adults with C1-esterase inhibitor deficiency. Jul 2017 Recommended no section in document
icatibant Symptomatic treatment of acute attacks of hereditary angioedema (HAE) in adults with C1-esterase-inhibitor deficiency. Nov 2016 Not recommended input received
icatibant Treatment of laryngeal/oro-pharyngeal and severe abdominal attacks of acute hereditary angioedema (HAE) for patients with confirmed diagnosis of C1-esterase… Jul 2010 Not recommended no section in document

Conditions are classified by a language model from the indication text of each submission, so an individual label here can be wrong. Consumer input is read from the document's own consumer comments section: 2 of 3 decisions since 2014 carried some. Silence means no comment reached the committee through that facility, not that nobody was affected. More on how this was built.