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Prevention of Hereditary Angioedema Attacks with a Subcutaneous C1 Inhibitor
Author(s) -
Hilary Longhurst,
Marco Cicardi,
Timothy Craig,
Konrad Bork,
Clive Grattan,
James Baker,
Henry Li,
Avner Reshef,
James R. Bonner,
Jonathan A. Bernstein,
John Anderson,
William Lumry,
Henriette Farkas,
Constance H. Katelaris,
Gordon Sussman,
Joshua Jacobs,
Marc A. Riedl,
Michael Manning,
Jacques Hébert,
Paul K. Keith,
Shmuel Kivity,
Sergio Neri,
Donald S. Levy,
M. L. Baeza,
Robert Nathan,
Lawrence B. Schwartz,
Teresa Caballero,
William H. Yang,
Ioana Crisan,
Dolores Hernández Fernández de Rojas,
Iftikhar Hussain,
Michael Tarzi,
Bruce Ritchie,
Pavlína Králíčková,
Mar Guilarte,
Syed M. Rehman,
Aleena Banerji,
Richard Gower,
Debra M. Bensen-Kennedy,
Jonathan M. Edelman,
Henrike Feuersenger,
JohnPhilip Lawo,
Thomas Machnig,
Dipti Pawaskar,
Ingo Pragst,
Bruce L. Zuraw
Publication year - 2017
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1613627
Subject(s) - medicine , hereditary angioedema , angioedema , c1 inhibitor , dermatology , medline , political science , law
Hereditary angioedema is a disabling, potentially fatal condition caused by deficiency (type I) or dysfunction (type II) of the C1 inhibitor protein. In a phase 2 trial, the use of CSL830, a nanofiltered C1 inhibitor preparation that is suitable for subcutaneous injection, resulted in functional levels of C1 inhibitor activity that would be expected to provide effective prophylaxis of attacks.

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