Garadacimab: First Approval
- 22-04-2025
- Hereditary Angioedema
- AdisInsight Report
- Author
- Simon Fung
- Published in
- Drugs | Issue 6/2025
Abstract
Garadacimab (Andembry®) is a fully human IgG4/lambda recombinant monoclonal anti-activated Factor XII antibody being developed by CSL Behring for the prevention of hereditary angioedema attacks. In January 2025, garadacimab received its first approval in Australia and the UK for prevention of hereditary angioedema attacks in adult and adolescent patients aged ≥ 12 years. Additionally, in February 2025, garadacimab was approved for the same indication in the EU, Japan and Switzerland. In the USA and Canada, regulatory review of garadacimab is currently underway. This article summarizes the milestones in the development of garadacimab leading to this first approval for prevention of recurrent hereditary angioedema attacks in adult and adolescent patients aged ≥ 12 years.
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- Title
- Garadacimab: First Approval
- Author
-
Simon Fung
- Publication date
- 22-04-2025
- Publisher
- Springer International Publishing
- Published in
-
Drugs / Issue 6/2025
Print ISSN: 0012-6667
Electronic ISSN: 1179-1950 - DOI
- https://doi.org/10.1007/s40265-025-02180-2
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