Correction to: Allergy Asthma Clin Immunol (2019) 15:72 https://doi.org/10.1186/s13223-019-0376-8
Following the publication of this article [1], the authors requested to amend the characterisation of ‘lanadelumab’ from ‘humanised’ to the correct ‘fully human’.
Therefore, the fourth paragraph under Recommendation #24 should be amended to read:
“Lanadelumab (Takeda), a fully human monoclonal antibody against kallikrein, takes approximately 70 days to reach a steady state concentration [110], and is therefore not recommended for STP…”
Similarly, the first paragraph under Recommendation #27 should be amended to read:
“Lanadelumab is a subcutaneously injectable, fully human, anti-active plasma kallikrein monoclonal antibody (IgG1/κ-light chain)…”
Reference
Betschel S, Badiou J, Binkley K, Borici-Mazi R, Hébert J, Kanani A, Keith P, Lacuesta G, Waserman S, Yang B, Aygören-Pürsün E, Bernstein J, Bork K, Caballero T, Cicardi M, Craig T, Farkas H, Grumach A, Katelaris C, Longhurst H, Riedl M, Zuraw B, Berger M, Boursiquot J-N, Boysen H, Castaldo A, Chapdelaine H, Connors L, Lisa F, Goodyear D, Haynes A, Kamra P, Kim H, Lang-Robertson K, Leith E, McCusker C, Moote B, O’Keefe A, Othman I, Poon M-C, Ritchie B, St-Pierre C, Stark D, Tsai E. The International/Canadian Hereditary Angioedema Guideline. Allergy Asthma Clin Immunol. 2019;15:72. https://doi.org/10.1186/s13223-019-0376-8.
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Betschel, S., Badiou, J., Binkley, K. et al. Correction to: The International/Canadian Hereditary Angioedema Guideline. Allergy Asthma Clin Immunol 16, 33 (2020). https://doi.org/10.1186/s13223-020-00430-4
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DOI: https://doi.org/10.1186/s13223-020-00430-4