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Angioedema Treatment Market - Global Industry Analysis 2025
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Frequent approval of novel drugs from regulatory bodies is expected to boost growth of global angioedema treatment market
In 2017, U.S. Food and Drug Administration approved Haegarda, a C1 Esterase Inhibitor (Human) for subcutaneous administration indicated for the preventing hereditary angioedema (HAE) in adult and adolescent patients. In 2014, Pharming Group NV and Salix Pharmaceuticals, Ltd. received US Food and Drug Administration (FDA) approval for RUCONEST (C1 Esterase Inhibitor [Recombinant]) 50 IU/kg, indicated for the treatment of acute angioedema attacks in adult and adolescent patients with HAE. In 2016, CSL Behring received FDA approval for Berinert [C1 Esterase Inhibitor (Human)], indicated for the treatment of HAE attacks in pediatric patients. These multiple approvals of new drugs by regulatory bodies are expected to drive growth of global angioedema treatment market over the forecast period. Furthermore, initiatives taken by various organizations to support treatment of angioedema is also expected to support the growth of global angioedema treatment market. For instance in 2015, British Society for Allergy and Clinical Immunology (BSACI) provided a guideline for the management of chronic urticaria and angioedema. In 2013, the World Allergy Organization (WAO) also provided guideline for the Management of Hereditary Angioedema.
Angioedema Treatment Market Taxonomy
The angioedema treatment market is segmented on the basis of condition type, drug type, route of administration, distribution channel, and geography
By Condition Type:
Allergic angioedema
Drug-induced angioedema
Idiopathic angioedema
Hereditary angioedema (HAE)
By Drug Type:
C1 esterase inhibitor
Cinryze
Berinert
Ruconest
Haegarda
Selective bradykinin B2 receptor antagonist
Firazyr
Kallikrein inhibitor
Kalbitor
Others
By Route of Administration:
Injection
Intravenous
Subcutaneous
Oral
By Distribution Channel
Hospitals
Retail pharmacies
Online pharmacies
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Europe angioedema treatment market is expected show significant growth, owing to increasing presence of angioedema drug manufacturers
Europe is expected to be the second largest market for global angioedema treatment and it is also projected to witness a significant growth over the forecast period, owing to increasing number of new manufacturing plant in region. For instance in January 2018, Shire plc received U.S. Food and Drug Administration approval for the technology transfer of CINRYZE (C1 esterase inhibitor [human]) drug product manufacturing process to Vienna, Austria manufacturing site. CINRYZE is an injectable prescription medicine indicated for the treatment of HAE in teenagers and adults. North America is expected to hold the dominant position in global angioedema treatment market due to approval of new drugs indicated for the treatment of angioedema. For instance in 2014, Shire Canada Inc. received approval for its FIRAZYR (icatibant injection) in Canada. FIRAZYR is indicated for the treatment of acute attacks of HAE in adults with C1-esterase inhibitor deficiency.
Key players in angioedema treatment market include Shire plc, CSL Limited, Pharming Group NV, Ionis Pharmaceuticals, Inc., iBio Inc., and BioCryst Pharmaceuticals, Inc. In 2017, Shire plc. received European Commission (EC) approval for label extension, that increases indication for FIRAZYR (icatibant injection), broadening use to adolescents and children aged 2 years and older, with HAE caused by C1-esterase-inhibitor (C1-INH) deficiency.
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