Literature DB >> 26556097

Icatibant for Multiple Hereditary Angioedema Attacks across the Controlled and Open-Label Extension Phases of FAST-3.

William R Lumry1, Henriette Farkas, Dumitru Moldovan, Elias Toubi, Jovanna Baptista, Timothy Craig, Marc Riedl.   

Abstract

BACKGROUND: In randomized, controlled, double-blind, multicenter phase 3 studies, one icatibant injection was efficacious and generally well tolerated in patients with a single hereditary angioedema (HAE) attack. Here, the efficacy and safety of icatibant for multiple HAE attacks was evaluated across the controlled and open-label extension phases of the For Angioedema Subcutaneous Treatment (FAST)-3 study (NCT00912093).
METHODS: In the controlled phase, adults with HAE type I or II were randomized (1:1) to receive a single subcutaneous injection of icatibant 30 mg or placebo within 6 h of an attack becoming mild (laryngeal) or moderate (cutaneous/abdominal). Open-label icatibant was administered for severe laryngeal symptoms. In the open-label extension phase, patients could receive up to three icatibant injections per attack. Efficacy and safety were analyzed for the first five icatibant-treated attacks at any location (prospective analysis) and laryngeal attacks (post hoc analysis) across both phases. Efficacy outcomes were based on patient-reported symptom severity (visual analog scale).
RESULTS: In groups of patients with one to five icatibant-treated attacks at any location (n = 88), the median times to onset of symptom relief, onset of primary symptom relief and almost complete symptom relief were 1.9-2.1, 1.5-2.0 and 3.5-19.7 h, respectively. The same outcomes for laryngeal attacks (n = 25) were 1.0-2.0, 1.0-2.0 and 1.5-8.1 h, respectively. The most frequently reported adverse events were a worsening or recurrence of HAE attack, headache and nasopharyngitis. Two serious adverse events (arrhythmia and noncardiac chest pain) were considered to be related to icatibant.
CONCLUSIONS: Icatibant was efficacious and generally well tolerated across multiple HAE attacks, including laryngeal attacks.
© 2015 S. Karger AG, Basel.

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Year:  2015        PMID: 26556097     DOI: 10.1159/000441060

Source DB:  PubMed          Journal:  Int Arch Allergy Immunol        ISSN: 1018-2438            Impact factor:   2.749


  4 in total

Review 1.  Clinical manifestations of hereditary angioedema and a systematic review of treatment options.

Authors:  Mattie Rosi-Schumacher; Sejal J Shah; Timothy Craig; Neerav Goyal
Journal:  Laryngoscope Investig Otolaryngol       Date:  2021-04-03

Review 2.  Optimum Use of Acute Treatments for Hereditary Angioedema: Evidence-Based Expert Consensus.

Authors:  Hilary Longhurst
Journal:  Front Med (Lausanne)       Date:  2018-03-12

3.  Fresh frozen plasma for on-demand hereditary angioedema treatment in South Africa and Iran.

Authors:  Nicole Wentzel; Angelica Panieri; Maryam Ayazi; Sipho Duncan Ntshalintshali; Zahra Pourpak; Di Hawarden; Paul Potter; Michael E Levin; Mohammad Reza Fazlollahi; Jonathan Peter
Journal:  World Allergy Organ J       Date:  2019-10-12       Impact factor: 4.084

Review 4.  Assessment and management of disease burden and quality of life in patients with hereditary angioedema: a consensus report.

Authors:  Konrad Bork; John T Anderson; Teresa Caballero; Timothy Craig; Douglas T Johnston; H Henry Li; Hilary J Longhurst; Cristine Radojicic; Marc A Riedl
Journal:  Allergy Asthma Clin Immunol       Date:  2021-04-19       Impact factor: 3.406

  4 in total

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