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Article: Becoming attack-free further improves health-related quality of life in patients with hereditary angioedema receiving garadacimab

TitleBecoming attack-free further improves health-related quality of life in patients with hereditary angioedema receiving garadacimab
Authors
Issue Date1-May-2025
PublisherOceanSide Publications; 1999
Citation
Allergy and Asthma Proceedings, 2025, v. 46, n. 3, p. 200-208 How to Cite?
AbstractBackground: Hereditary angioedema (HAE) is associated with substantial health-related quality of life (HRQoL) impairments. Complete disease control and life normalization are key treatment goals. In previous studies, garadacimab prevented HAE attacks with a favorable safety profile and HRQoL improvements. Objective: HRQoL was evaluated in patients with HAE receiving garadacimab stratified by attack-free status. Methods: In the pivotal phase III study (NCT04656418), 39 patients received garadacimab 200 mg subcutaneously once monthly and 25 volume-matched placebo. In the phase III open-label extension (OLE), 90 patients in the garadacimab-naive group (received placebo in previous studies or newly enrolled) and 71 patients in the previous garadacimab exposure group (received garadacimab in previous studies) received garadacimab (NCT04739059). Patients ages ≥ 18 years completed the Angioedema Quality of Life (AE-QoL) questionnaire in both studies; scores were evaluated post hoc by attack-free status. Results: In the pivotal phase III and phase III OLE studies, 62% and 60% of patients, respectively, were attack-free. In the pivotal phase III study, the mean AE-QoL total score improved with garadacimab, from 38.8 (day 1) to 6.6 (month 6) for attack-free patients (n = 19) and to 18.4 for patients with one or more attacks (n = 14) versus a change in mean AE-QoL total score from 43.7 to 40.5 with placebo (n = 20). In the phase III OLE study, the mean AE-QoL total score for patients who were garadacimab naive decreased from 46.2 (day 1) to 8.6 (month 12) for attack-free patients (n = 34) and from 54.5 to 23.5 for patients with one or more attacks (n = 30). For the previous garadacimab exposure group, AE-QoL improvements were maintained from previous studies, regardless of attack-free status. Conclusion: Garadacimab was associated with HRQoL improvement versus run-in in all groups. After garadacimab exposure in previous studies, improvements were maintained in the phase III OLE study. Attack-free patients had the greatest HRQoL improvements, bringing them closer to complete disease control and life normalization.
Persistent Identifierhttp://hdl.handle.net/10722/357734
ISSN
2023 Impact Factor: 2.6
2023 SCImago Journal Rankings: 0.630
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorStaubach, Petra-
dc.contributor.authorCraig, Timothy J.-
dc.contributor.authorFukuda, Tomoo-
dc.contributor.authorAygoren-Pursun, Emel-
dc.contributor.authorHakl, Roman-
dc.contributor.authorBraverman, Julia-
dc.contributor.authorLawo, John Philip-
dc.contributor.authorPollen, Maressa-
dc.contributor.authorNenci, Chiara-
dc.contributor.authorLi, Philip H.-
dc.contributor.authorFarkas, Henriette-
dc.date.accessioned2025-07-22T03:14:36Z-
dc.date.available2025-07-22T03:14:36Z-
dc.date.issued2025-05-01-
dc.identifier.citationAllergy and Asthma Proceedings, 2025, v. 46, n. 3, p. 200-208-
dc.identifier.issn1088-5412-
dc.identifier.urihttp://hdl.handle.net/10722/357734-
dc.description.abstractBackground: Hereditary angioedema (HAE) is associated with substantial health-related quality of life (HRQoL) impairments. Complete disease control and life normalization are key treatment goals. In previous studies, garadacimab prevented HAE attacks with a favorable safety profile and HRQoL improvements. Objective: HRQoL was evaluated in patients with HAE receiving garadacimab stratified by attack-free status. Methods: In the pivotal phase III study (NCT04656418), 39 patients received garadacimab 200 mg subcutaneously once monthly and 25 volume-matched placebo. In the phase III open-label extension (OLE), 90 patients in the garadacimab-naive group (received placebo in previous studies or newly enrolled) and 71 patients in the previous garadacimab exposure group (received garadacimab in previous studies) received garadacimab (NCT04739059). Patients ages ≥ 18 years completed the Angioedema Quality of Life (AE-QoL) questionnaire in both studies; scores were evaluated post hoc by attack-free status. Results: In the pivotal phase III and phase III OLE studies, 62% and 60% of patients, respectively, were attack-free. In the pivotal phase III study, the mean AE-QoL total score improved with garadacimab, from 38.8 (day 1) to 6.6 (month 6) for attack-free patients (n = 19) and to 18.4 for patients with one or more attacks (n = 14) versus a change in mean AE-QoL total score from 43.7 to 40.5 with placebo (n = 20). In the phase III OLE study, the mean AE-QoL total score for patients who were garadacimab naive decreased from 46.2 (day 1) to 8.6 (month 12) for attack-free patients (n = 34) and from 54.5 to 23.5 for patients with one or more attacks (n = 30). For the previous garadacimab exposure group, AE-QoL improvements were maintained from previous studies, regardless of attack-free status. Conclusion: Garadacimab was associated with HRQoL improvement versus run-in in all groups. After garadacimab exposure in previous studies, improvements were maintained in the phase III OLE study. Attack-free patients had the greatest HRQoL improvements, bringing them closer to complete disease control and life normalization.-
dc.languageeng-
dc.publisherOceanSide Publications; 1999-
dc.relation.ispartofAllergy and Asthma Proceedings-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleBecoming attack-free further improves health-related quality of life in patients with hereditary angioedema receiving garadacimab-
dc.typeArticle-
dc.identifier.doi10.2500/aap.2025.46.250026-
dc.identifier.pmid40380356-
dc.identifier.scopuseid_2-s2.0-105005492329-
dc.identifier.volume46-
dc.identifier.issue3-
dc.identifier.spage200-
dc.identifier.epage208-
dc.identifier.isiWOS:001517494500012-
dc.identifier.issnl1088-5412-

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