[HTML][HTML] Assessment and management of disease burden and quality of life in patients with hereditary angioedema: a consensus report

K Bork, JT Anderson, T Caballero, T Craig… - Allergy, Asthma & …, 2021 - Springer
Background Hereditary angioedema (HAE) is a rare disease characterized by
unpredictable, potentially life-threatening attacks, resulting in significant physical and …

[HTML][HTML] The international WAO/EAACI guideline for the management of hereditary angioedema–The 2021 revision and update

M Maurer, M Magerl, S Betschel, W Aberer… - World Allergy …, 2022 - Elsevier
Hereditary Angioedema (HAE) is a rare and disabling disease for which early diagnosis and
effective therapy are critical. This revision and update of the global WAO/EAACI guideline on …

Angiotensin-converting enzyme inhibitor–induced angioedema

RG Wilkerson, ME Winters - Emergency Medicine Clinics, 2022 - emed.theclinics.com
Background ACEi medications were developed after it was noted that people bitten by the
Brazilian pit viper Bothrops jararaca developed profound hypotension and frequently died …

[HTML][HTML] Inhibition of prekallikrein for hereditary angioedema

LM Fijen, MA Riedl, L Bordone… - … England Journal of …, 2022 - Mass Medical Soc
Background Hereditary angioedema is characterized by recurrent and unpredictable
swellings that are disabling and potentially fatal. Selective inhibition of plasma prekallikrein …

Prophylactic use of an anti-activated factor XII monoclonal antibody, garadacimab, for patients with C1-esterase inhibitor-deficient hereditary angioedema: a …

T Craig, M Magerl, DS Levy, A Reshef, WR Lumry… - The Lancet, 2022 - thelancet.com
Background Hereditary angioedema is associated with dysregulation of the kallikrein–kinin
system. Factor XII (FXII) is a key initiator of the kallikrein–kinin system, which produces …

Efficacy and safety of garadacimab, a factor XIIa inhibitor for hereditary angioedema prevention (VANGUARD): a global, multicentre, randomised, double-blind …

TJ Craig, A Reshef, HH Li, JS Jacobs, JA Bernstein… - The Lancet, 2023 - thelancet.com
Background Hereditary angioedema is a rare and potentially life-threatening genetic
disease that is associated with kallikrein–kinin system dysregulation. Garadacimab …

Long‐term prevention of hereditary angioedema attacks with lanadelumab: The HELP OLE Study

A Banerji, JA Bernstein, DT Johnston, WR Lumry… - Allergy, 2022 - Wiley Online Library
Background The aim was to evaluate long‐term effectiveness and safety of lanadelumab in
patients≥ 12 y old with hereditary angioedema (HAE) 1/2 (NCT02741596). Methods …

Long‐term safety and effectiveness of berotralstat for hereditary angioedema: The open‐label APeX‐S study

H Farkas, M Stobiecki, J Peter… - Clinical and …, 2021 - Wiley Online Library
Background Berotralstat (BCX7353) is an oral, once‐daily inhibitor of plasma kallikrein
recently approved for prevention of angioedema attacks in adults and adolescents with …

Epidemiology, management, and treatment access of hereditary angioedema in the Asia Pacific region: outcomes from an international survey

PH Li, R Pawankar, BYH Thong, JS Fok… - The Journal of Allergy …, 2023 - Elsevier
Background Hereditary angioedema (HAE) is a rare genetic disease with significant
morbidity and mortality for which early diagnosis and effective therapy are critical. Many Asia …

[HTML][HTML] Randomized trial of the efficacy and safety of berotralstat (BCX7353) as an oral prophylactic therapy for hereditary angioedema: results of APeX-2 through 48 …

HJ Wedner, E Aygören-Pürsün, J Bernstein… - The Journal of Allergy …, 2021 - Elsevier
Background Berotralstat (BCX7353) is a recently approved, oral, once-daily kallikrein
inhibitor for hereditary angioedema (HAE) prophylaxis. In the APeX-2 trial, berotralstat …