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Treatment of acute attacks of hereditary angioedema (HAE) with the bradykinin B2 receptor antagonist icatibant

Filename 37. Magerl et al.,HAE B2 receptor,Rev. Port. de Imunoalerg.2010.pdf
Filesize 161,74 kB
Version r.037
Date added Juni 26, 2020
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Category Reviews
Tags bradykinin, Hereditary Angioedema, Icatibant
Authors Magerl, M., Keßler, B., and Maurer, M.
Citation Magerl, M., Keßler, B., and Maurer, M.: Treatment of acute attacks of hereditary angioedema (HAE) with the bradykinin B2 receptor antagonist icatibant. Rev. Port. Imunoalergologia 2010: 18; 207-214.
Corresponding authors Maurer, M.
DocNum R.37
DocType PDF
Edition; Page 18; 207-214
IF N/A
Publisher Rev. Port. Imunoalergologia
ReleaseDate 2010

Icatibant is a selective and competitive bradykinin B2 receptor antagonist. It was approved in 2008, for the symptomatic treatment of acute attacks of hereditary angioedema (HAE) in adults with a deficiency of the C1 esterase inhibitor. Icatibant is the first subcutaneous treatment for HAE. The efficacy of icatibant in the treatment of moderate to very severe cutaneous and abdominal attacks in patients with HAE was investigated in two Phase III trials in comparison with tranexamic acid and with placebo, respectively. The time to onset of symptom relief, the primary end point of the trial, was significantly shortened with icatibant compared to tranexamic acid. Icatibant demonstrated a favourable safety profile in clinical trials with no drug-related serious adverse events.

 

(Last update: 12.2023)

Number of original publications in peer-reviewed journals:580
Number of reviews in peer-reviewed journals:210
Number of publications (original work and reviews) in peer-reviewed journals:790
Cumulative IF for original publications in peer-reviewed journals:4196.39
Cumulative IF for reviews in peer-reviewed journals:1409.32
Cumulative IF of publications (original work & reviews) in peer-reviewed journals:5605.71
Total number of citations: 36,836, h-index: 99 (Web of Science December 2023)36836

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